2025-05-09 18:23:27, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001199104 2982 bp mRNA linear PRI 07-JUL-2013 DEFINITION Homo sapiens NT5C1B-RDH14 readthrough (NT5C1B-RDH14), transcript variant 2, mRNA. ACCESSION NM_001199104 VERSION NM_001199104.1 GI:312283683 KEYWORDS RefSeq. SOURCE Homo sapiens (human) ORGANISM Homo sapiens Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. REFERENCE 1 (bases 1 to 2982) AUTHORS Prakash,T., Sharma,V.K., Adati,N., Ozawa,R., Kumar,N., Nishida,Y., Fujikake,T., Takeda,T. and Taylor,T.D. TITLE Expression of conjoined genes: another mechanism for gene regulation in eukaryotes JOURNAL PLoS ONE 5 (10), E13284 (2010) PUBMED 20967262 REMARK Publication Status: Online-Only COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AC079148.9 and AK057444.1. Summary: This locus represents naturally occurring read-through transcription between the neighboring NT5C1B (5'-nucleotidase, cytosolic IB) and RDH14 (retinol dehydrogenase 14) genes on chromosome 2. Alternative splicing results in multiple transcript variants, one of which encodes a fusion protein that shares sequence identity with the products of each individual gene. [provided by RefSeq, Nov 2010]. Transcript Variant: This variant (2) includes an additional in-frame exon in the 5' coding region, an alternate in-frame splice site in the central coding region, and an additional exon that causes a frameshift in the 3' coding region, compared to variant 1. The encoded isoform (2) is shorter and has a distinct C-terminus, and it lacks sequence identity with the RDH14 product, compared to isoform 1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. ##Evidence-Data-START## Transcript exon combination :: AK057444.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support ERS025084, ERS025085 [ECO:0000350] ##Evidence-Data-END## ##RefSeq-Attributes-START## readthrough transcript :: includes exons from GeneID 57665, 93034 ##RefSeq-Attributes-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-18 AC079148.9 144226-144243 c 19-2160 AK057444.1 1-2142 2161-2982 AC079148.9 109386-110207 c FEATURES Location/Qualifiers source 1..2982 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="2" /map="2p" gene 1..2982 /gene="NT5C1B-RDH14" /note="NT5C1B-RDH14 readthrough" /db_xref="GeneID:100526794" /db_xref="HGNC:38831" exon 1..142 /gene="NT5C1B-RDH14" /inference="alignment:Splign:1.39.8" misc_feature 8..10 /gene="NT5C1B-RDH14" /note="upstream in-frame stop codon" variation complement(92) /gene="NT5C1B-RDH14" /replace="a" /replace="t" /db_xref="dbSNP:368657100" variation complement(93) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:375020758" variation complement(102) /gene="NT5C1B-RDH14" /replace="a" /replace="c" /db_xref="dbSNP:370091625" CDS 113..1921 /gene="NT5C1B-RDH14" /note="isoform 2 is encoded by transcript variant 2; NT5C1B-RDH14 read-through transcript" /codon_start=1 /product="NT5C1B-RDH14 protein isoform 2" /protein_id="NP_001186033.1" /db_xref="GI:312283684" /db_xref="CCDS:CCDS56111.1" /db_xref="GeneID:100526794" /db_xref="HGNC:38831" /translation="
MSQTSLKQKKNEPGMRSSKESLEAEKRKESDKTGVRLSNQMRRAVNPNHSLRCCPFQGHSSCRRCLCAAEGTALGPCHTIRIYIHMCLLWEQGQQITMMRGSQESSLRKTDSRGYLVRSQWSRISRSPSTKAPSIDEPRSRNTSAKLPSSSTSSRTPSTSPSLHDSSPPPLSGQPSLQPPASPQLPRSLDSRPPTPPEPDPGSRRSTKMQENPEAWAQGIVREIRQTRDSQPLEYSRTSPTEWKSSSQRRGIYPASTQLDRNSLSEQQQQQREDEDDYEAAYWASMRSFYEKNPSCSRPWPPKPKNAITIALSSCALFNMVDGRKIYEQEGLEKYMEYQLTNENVILTPGPAFRFVKALQYVNARLRDLYPDEQDLFDIVLMTNNHAQVGVRLINSVNHYGLLIDRFCLTGGKDPIGYLKAYLTNLYIAADSEKVQEAIQEGIASATMFDGAKDMAYCDTQLRVAFDGDAVLFSDESEHFTKEHGLDKFFQYDTLCESKPLAQGPLKGFLEDLGRLQKKFYAKNERLLCPIRTYLVTARSAASSGARVLKTLRRWGLEIDEALFLAGAPKSPILVKIRPHIFFDDHMFHIEGAQRKSLGWMS
" misc_feature 1121..1897 /gene="NT5C1B-RDH14" /note="5'-nucleotidase; Region: 5-nucleotidase; pfam06189" /db_xref="CDD:148034" variation complement(133) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:17852342" exon 143..232 /gene="NT5C1B-RDH14" /inference="alignment:Splign:1.39.8" variation complement(148) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:139661780" variation complement(151) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:16985306" variation complement(152) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:150854562" variation complement(173) /gene="NT5C1B-RDH14" /replace="a" /replace="t" /db_xref="dbSNP:142250232" variation complement(178) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:373948064" variation complement(219) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:368786487" exon 233..412 /gene="NT5C1B-RDH14" /inference="alignment:Splign:1.39.8" variation complement(240) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:144387028" variation complement(251) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:140803100" variation complement(259) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:369042120" variation complement(261) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:373286312" variation complement(262) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:76041976" variation complement(271) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:3810839" variation complement(292) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:200114668" variation complement(302) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:199544140" variation complement(313) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:376548938" variation complement(324) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:367989070" variation complement(353) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:113913452" variation complement(354) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:150116798" variation complement(361) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:369072062" variation complement(368) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:376686535" variation complement(371) /gene="NT5C1B-RDH14" /replace="a" /replace="t" /db_xref="dbSNP:373559057" exon 413..550 /gene="NT5C1B-RDH14" /inference="alignment:Splign:1.39.8" variation complement(421) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:147993928" variation complement(431) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:201679289" variation complement(432) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:147855918" variation complement(434) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:375353460" variation complement(435) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:142174343" variation complement(449) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:114622083" variation complement(450) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:199873248" variation complement(461) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:200122449" variation complement(462) /gene="NT5C1B-RDH14" /replace="g" /replace="t" /db_xref="dbSNP:371760155" variation complement(465) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:367871143" variation complement(489) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:202225134" variation complement(502) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:371117462" variation complement(509) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:368550960" variation complement(518) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:201205997" variation complement(525) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:200286986" exon 551..1015 /gene="NT5C1B-RDH14" /inference="alignment:Splign:1.39.8" variation complement(589) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:61741495" variation complement(604) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:117298882" variation complement(622) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:200689028" variation complement(639) /gene="NT5C1B-RDH14" /replace="a" /replace="c" /db_xref="dbSNP:61742596" variation complement(672) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:61742608" variation complement(687) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:368950263" variation complement(764) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:369345171" variation complement(769) /gene="NT5C1B-RDH14" /replace="a" /replace="c" /db_xref="dbSNP:200514864" variation complement(794) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:373347393" variation complement(795) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:150624428" variation complement(807) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:369846764" variation complement(808) /gene="NT5C1B-RDH14" /replace="g" /replace="t" /db_xref="dbSNP:200273135" variation complement(811) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:144486690" variation complement(825) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:201047201" variation complement(861) /gene="NT5C1B-RDH14" /replace="g" /replace="t" /db_xref="dbSNP:76782074" variation complement(880) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:377296218" variation complement(887) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:202208251" variation complement(900) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:146399000" variation complement(924..926) /gene="NT5C1B-RDH14" /replace="" /replace="agc" /db_xref="dbSNP:145060005" variation complement(929) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:200906490" variation complement(934) /gene="NT5C1B-RDH14" /replace="a" /replace="c" /db_xref="dbSNP:191446499" variation complement(950) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:199965310" variation complement(977) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:113101936" variation complement(994..995) /gene="NT5C1B-RDH14" /replace="" /replace="a" /db_xref="dbSNP:34127788" variation complement(994) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:372417853" exon 1016..1183 /gene="NT5C1B-RDH14" /inference="alignment:Splign:1.39.8" variation complement(1084) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:151116969" variation complement(1088) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:370362544" variation complement(1093) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:376326986" variation complement(1109) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:372553926" variation complement(1123) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:16985301" variation complement(1127) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:138883415" variation complement(1139) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:140827083" variation complement(1168) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:145994780" exon 1184..1313 /gene="NT5C1B-RDH14" /inference="alignment:Splign:1.39.8" variation complement(1211) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:113497432" variation complement(1248) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:369708621" variation complement(1264) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:145263582" variation complement(1286) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:183534911" variation complement(1301) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:144184703" variation complement(1312) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:148193506" exon 1314..1436 /gene="NT5C1B-RDH14" /inference="alignment:Splign:1.39.8" variation complement(1319) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:150673884" variation complement(1328) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:148419532" variation complement(1329) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:142671746" variation complement(1333) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:146130311" variation complement(1335) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:149545160" variation complement(1342) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:140315086" variation complement(1343) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:145698850" variation complement(1390) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:140510680" variation complement(1406) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:148789216" variation complement(1418) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:145414794" exon 1437..1621 /gene="NT5C1B-RDH14" /inference="alignment:Splign:1.39.8" variation complement(1477) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:373568974" variation complement(1496) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:117487981" variation complement(1500) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:201567504" variation complement(1511) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:368221092" variation complement(1538) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:147377645" variation complement(1547) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:140280643" variation complement(1570) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:3902946" variation complement(1575) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:149286164" variation complement(1609) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:369771689" exon 1622..1896 /gene="NT5C1B-RDH14" /inference="alignment:Splign:1.39.8" variation complement(1666) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:147103410" variation complement(1667) /gene="NT5C1B-RDH14" /replace="a" /replace="t" /db_xref="dbSNP:79178256" variation complement(1687) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:376888692" variation complement(1688) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:201315955" variation complement(1691) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:112808478" variation complement(1773) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:147855687" variation complement(1779) /gene="NT5C1B-RDH14" /replace="g" /replace="t" /db_xref="dbSNP:200342649" variation complement(1788) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:146822895" variation complement(1789) /gene="NT5C1B-RDH14" /replace="a" /replace="t" /db_xref="dbSNP:201665017" variation complement(1793) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:140939592" variation complement(1794) /gene="NT5C1B-RDH14" /replace="a" /replace="c" /db_xref="dbSNP:144165826" variation complement(1832) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:374183150" variation complement(1852) /gene="NT5C1B-RDH14" /replace="a" /replace="c" /db_xref="dbSNP:202025887" variation complement(1864) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:142999822" variation complement(1881) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:147939092" exon 1897..2982 /gene="NT5C1B-RDH14" /inference="alignment:Splign:1.39.8" variation complement(1978) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:375822735" variation complement(2021) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:149867802" variation complement(2030) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:141384613" variation complement(2065) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:377520259" variation complement(2094) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:138658701" variation complement(2095) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:201424633" variation complement(2136) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:373055751" variation complement(2138) /gene="NT5C1B-RDH14" /replace="a" /replace="t" /db_xref="dbSNP:138843648" variation complement(2161) /gene="NT5C1B-RDH14" /replace="a" /replace="c" /db_xref="dbSNP:201455737" STS 2166..2973 /gene="NT5C1B-RDH14" /standard_name="RDH14__5475" /db_xref="UniSTS:463857" variation complement(2193) /gene="NT5C1B-RDH14" /replace="a" /replace="c" /db_xref="dbSNP:185675117" variation complement(2197) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:373938743" variation complement(2200) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:143289874" variation complement(2204) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:201623319" variation complement(2224) /gene="NT5C1B-RDH14" /replace="a" /replace="t" /db_xref="dbSNP:138173772" variation complement(2231) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:141886106" variation complement(2252) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:141569821" variation complement(2265) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:142589700" variation complement(2284) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:199868568" variation complement(2295) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:371846340" variation complement(2297) /gene="NT5C1B-RDH14" /replace="a" /replace="t" /db_xref="dbSNP:200669704" variation complement(2300) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:144461545" variation complement(2302) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:139953107" variation complement(2309) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:201317560" variation complement(2313) /gene="NT5C1B-RDH14" /replace="g" /replace="t" /db_xref="dbSNP:199674055" variation complement(2341) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:74378191" variation complement(2358) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:72775091" variation complement(2407) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:200234641" variation complement(2449) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:368455068" variation complement(2465) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:373588347" variation complement(2533) /gene="NT5C1B-RDH14" /replace="c" /replace="g" /db_xref="dbSNP:201282431" variation complement(2536) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:376900863" variation complement(2549) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:375620361" variation complement(2553) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:370947814" variation complement(2579) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:148385113" variation complement(2601) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:375607315" variation complement(2707) /gene="NT5C1B-RDH14" /replace="a" /replace="t" /db_xref="dbSNP:115362218" variation complement(2767) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:111233807" STS 2782..2919 /gene="NT5C1B-RDH14" /standard_name="RH102895" /db_xref="UniSTS:97229" variation complement(2805) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:190845828" variation complement(2838) /gene="NT5C1B-RDH14" /replace="c" /replace="t" /db_xref="dbSNP:367551928" variation complement(2933) /gene="NT5C1B-RDH14" /replace="a" /replace="g" /db_xref="dbSNP:186442746" variation complement(2976) /gene="NT5C1B-RDH14" /replace="a" /replace="t" /db_xref="dbSNP:180786126" ORIGIN
ataaatttgacattctaaatgcaaagctagactgagcaagggaagtgacaggaaatggagctggggagacaaaaatgtggataacaacaaaagaatttcaacaggtaaaaaaatgagtcaaacatctctcaaacagaaaaagaatgagcctggaatgaggtcctcaaaagagagtctagaagcagaaaaaagaaaggaatctgacaaaacaggagttcgtctgagcaatcagatgaggcgtgcagtcaatccgaatcactcgctgagatgttgccccttccagggtcactcgtcgtgtagacgctgcctttgtgcagctgagggaacagcccttggcccctgccacacaatacgtatttatattcacatgtgcctgttgtgggagcagggccagcagatcaccatgatgaggggatcacaagaatcatcactgcggaagacagactctcgagggtaccttgtgcgcagtcaatggtctagaatatcccggagcccatccaccaaggctccatccatagatgagcctagaagcaggaacaccagtgctaagctccccagcagctccacgagctcccggactccatccacctccccaagcctgcatgactcctcaccgccgccgctgtccgggcagccctcgctccagccacccgcgtcgccccagctgccccggtcgctggactcgcggcctcccacgcccccagagcccgatcctggctcccggcgcagcaccaaaatgcaagagaatccggaggcctgggcccaaggcatcgtgcgggaaatccgccagacccgggactcgcagccgctggaatattcgcgcacgtcccccaccgagtggaagtcctccagccagcgcagggggatctaccccgcctccacccagctggaccgcaactctctgtccgagcagcagcagcagcagcgggaggacgaggacgactacgaggctgcctactgggcatccatgaggtcgttctacgagaagaacccgagctgctcgcgcccctggccgcccaaacccaagaacgccatcaccattgctctctcatcctgcgcgctcttcaacatggtggacggcaggaaaatctacgagcaagagggtctggaaaagtacatggagtatcagctcaccaatgagaacgtcatcctgaccccgggcccggcgttccgcttcgtcaaggcactacagtatgtcaatgctagactccgtgatctatatcctgatgaacaggacttatttgatattgtactgatgactaataaccatgcccaagtgggagtgcggcttataaacagcgtcaatcactacggcttactgattgaccgcttctgtctgaccgggggaaaagaccccattggctatttgaaggcatatcttaccaacttgtatattgctgcagattctgaaaaagtgcaagaggcaatacaagaaggtattgcctctgcgacaatgtttgatggagccaaagacatggcttactgtgacactcagctccgtgtagcctttgatggggatgctgtcctcttctctgatgagtctgaacattttaccaaggagcatgggctcgacaaattcttccagtatgatacattatgtgaaagtaagcctcttgctcagggtcccctaaaaggctttctggaagatttaggcagactgcaaaagaagttctatgccaaaaatgaacggttactttgtcctatcaggacctacctggttacagctaggagtgcagccagttcaggcgcccgtgtgctgaagacccttcgacgctggggtctagagatagacgaagctcttttccttgctggagcccccaaaagtcccatcttggtgaagatccggccccacatcttctttgatgaccacatgttccacattgaaggggcacagaggaagagcctaggctggatgtcttgatcaataacgcagggatcttccagtgcccttacatgaagactgaagatgggtttgagatgcagttcggagtgaaccatctggggcactttctactcaccaatcttctccttggactcctcaaaagttcagctcccagcaggattgtggtagtttcttccaaactttataaatacggagacatcaattttgatgacttgaacagtgaacaaagctataataaaagcttttgttatagccggagcaaactggctaacattctttttaccagggaactagcccgccgcttagaaggcacaaatgtcaccgtcaatgtgttgcatcctggtattgtacggacaaatctggggaggcacatacacattccactgttggtcaaaccactcttcaatttggtgtcatgggcttttttcaaaactccagtagaaggtgcccagacttccatttatttggcctcttcacctgaggtagaaggagtgtcaggaagatactttggggattgtaaagaggaagaactgttgcccaaagctatggatgaatctgttgcaagaaaactctgggatatcagtgaagtgatggttggcctgctaaaataggaacaaggagtaaaagagctgtttataaaactgcatatcagttatatctgtgatcaggaatggtgtggattgagaacttgttacttgaagaaaaagaattttgatattggaatagcctgctaagaggtacatgtgggtattttggagttactgaaaaattatttttgggataagagaatttcagcaaagatgttttaaatatatatagtaagtataatgaataataagtacaatgaaaaatacaattatattgtaaaattataactgggcaagcatggatgacatattaatatttgtcagaattaagtgactcaaagtgctatcgagaggtttttcaagtatctttgagtttcatggccaaagtgttaactagttttactacaatgtttggtgtttgtgtggaaattatctgcctggtgtgtgcacacaagtcttacttggaataaatttactggtacaaattcttaa
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