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Variants search result for Homo sapiens
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49 records found for search term Rcbtb2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156164860CV2195918single nucleotide variantNM_001268.4(RCBTB2):c.98T>C (p.Ile33Thr)not specified [RCV004072177]uncertain significance134851568648515686Humanname
155950406CV2267846single nucleotide variantNM_001268.4(RCBTB2):c.72G>C (p.Lys24Asn)not specified [RCV004136147]uncertain significance134851571248515712Humanname
597764466CV3582858single nucleotide variantNM_001268.4(RCBTB2):c.28G>A (p.Gly10Arg)not specified [RCV004849786]uncertain significance134852191248521912Humanname
155971356CV2335678single nucleotide variantNM_001268.4(RCBTB2):c.142G>C (p.Ala48Pro)not specified [RCV004193879]uncertain significance134851564248515642Humanname
156212944CV2367009single nucleotide variantNM_001268.4(RCBTB2):c.193G>A (p.Asp65Asn)not specified [RCV004213411]uncertain significance134851559148515591Humanname
329382729CV2424536single nucleotide variantNM_001268.4(RCBTB2):c.247G>A (p.Val83Ile)not specified [RCV004254037]uncertain significance134851530748515307Humanname
401859910CV2765197single nucleotide variantNM_001268.4(RCBTB2):c.269G>A (p.Arg90Gln)not specified [RCV004339725]uncertain significance134851528548515285Humanname
598255271CV3898990single nucleotide variantNM_001268.4(RCBTB2):c.254G>C (p.Ser85Thr)not specified [RCV005259861]uncertain significance134851530048515300Humanname
8627459CV82603single nucleotide variantNM_001268.3(RCBTB2):c.1230C>T (p.Val410=)Malignant melanoma [RCV000062683]not provided134850175648501756Humanname
156379335CV2207941single nucleotide variantNM_001268.4(RCBTB2):c.377A>G (p.Asn126Ser)not specified [RCV004084358]uncertain significance134851286848512868Humanname
156104788CV2311068single nucleotide variantNM_001268.4(RCBTB2):c.631G>A (p.Ala211Thr)not specified [RCV004164073]uncertain significance134851206048512060Humanname
329393716CV2449813single nucleotide variantNM_001268.4(RCBTB2):c.889C>A (p.Gln297Lys)not specified [RCV004268915]uncertain significance134851066648510666Humanname
401888428CV2761289single nucleotide variantNM_001268.4(RCBTB2):c.775G>A (p.Val259Ile)not specified [RCV004341160]uncertain significance134851177848511778Humanname
401898277CV2791152single nucleotide variantNM_001268.4(RCBTB2):c.845G>C (p.Gly282Ala)not specified [RCV004356514]uncertain significance134851071048510710Humanname
405682441CV3319336single nucleotide variantNM_001268.4(RCBTB2):c.922G>A (p.Asp308Asn)not specified [RCV004443604]uncertain significance134851063348510633Humanname
407532100CV3465135single nucleotide variantNM_001268.4(RCBTB2):c.344C>T (p.Thr115Ile)not specified [RCV004657966]uncertain significance134851521048515210Humanname
407532102CV3465136single nucleotide variantNM_001268.4(RCBTB2):c.645G>A (p.Met215Ile)not specified [RCV004657967]uncertain significance134851204648512046Humanname
407507515CV3465137single nucleotide variantNM_001268.4(RCBTB2):c.847G>A (p.Ala283Thr)not specified [RCV004671750]uncertain significance134851070848510708Humanname
597729236CV3582852single nucleotide variantNM_001268.4(RCBTB2):c.968C>G (p.Ala323Gly)not specified [RCV004862893]uncertain significance134850287348502873Humanname
597764443CV3582853single nucleotide variantNM_001268.4(RCBTB2):c.433A>G (p.Ile145Val)not specified [RCV004849781]uncertain significance134851281248512812Humanname
597764454CV3582855single nucleotide variantNM_001268.4(RCBTB2):c.437C>T (p.Ser146Phe)not specified [RCV004849783]uncertain significance134851280848512808Humanname
597764458CV3582856single nucleotide variantNM_001268.4(RCBTB2):c.815T>C (p.Leu272Ser)not specified [RCV004849784]uncertain significance134851074048510740Humanname
598255276CV3898991single nucleotide variantNM_001268.4(RCBTB2):c.620T>C (p.Val207Ala)not specified [RCV005259862]uncertain significance134851207148512071Humanname
598255288CV3898993single nucleotide variantNM_001268.4(RCBTB2):c.587G>A (p.Arg196Gln)not specified [RCV005259864]uncertain significance134851210448512104Humanname
156176848CV2205353single nucleotide variantNM_001268.4(RCBTB2):c.1345T>C (p.Tyr449His)not specified [RCV004079964]uncertain significance134849966048499660Humanname
156019393CV2230008single nucleotide variantNM_001268.4(RCBTB2):c.1062C>G (p.Asp354Glu)not specified [RCV004105813]uncertain significance134850277948502779Humanname
156003091CV2258028single nucleotide variantNM_001268.4(RCBTB2):c.1315C>G (p.Pro439Ala)not specified [RCV004129826]uncertain significance134849969048499690Humanname
155988826CV2259610single nucleotide variantNM_001268.4(RCBTB2):c.1066G>A (p.Val356Met)not specified [RCV004116653]uncertain significance134850277548502775Humanname
156076305CV2281578single nucleotide variantNM_001268.4(RCBTB2):c.1378G>A (p.Ala460Thr)not specified [RCV004153879]uncertain significance134849962748499627Humanname
156147577CV2289488single nucleotide variantNM_001268.4(RCBTB2):c.1262C>T (p.Ser421Leu)not specified [RCV004154218]uncertain significance134849974348499743Humanname
156101923CV2291428single nucleotide variantNM_001268.4(RCBTB2):c.1457G>C (p.Gly486Ala)not specified [RCV004155759]uncertain significance134849624948496249Humanname
156062128CV2320964single nucleotide variantNM_001268.4(RCBTB2):c.1580G>A (p.Gly527Asp)not specified [RCV004172766]uncertain significance134849018748490187Humanname
156307924CV2332169single nucleotide variantNM_001268.4(RCBTB2):c.1093G>A (p.Val365Ile)not specified [RCV004189205]uncertain significance134850274848502748Humanname
155923621CV2347537single nucleotide variantNM_001268.4(RCBTB2):c.1013G>A (p.Arg338Gln)not specified [RCV004200480]uncertain significance134850282848502828Humanname
155910957CV2366769single nucleotide variantNM_001268.4(RCBTB2):c.1480G>A (p.Ala494Thr)not specified [RCV004210762]uncertain significance134849622648496226Humanname
155906233CV2393909single nucleotide variantNM_001268.4(RCBTB2):c.1085C>T (p.Thr362Met)not specified [RCV004233728]uncertain significance134850275648502756Humanname
401735723CV2695385single nucleotide variantNM_001268.4(RCBTB2):c.1324C>T (p.Arg442Trp)not specified [RCV004305590]uncertain significance134849968148499681Humanname
401887790CV2770444single nucleotide variantNM_001268.4(RCBTB2):c.1336G>A (p.Glu446Lys)not specified [RCV004358084]uncertain significance134849966948499669Humanname
401890737CV2775606single nucleotide variantNM_001268.4(RCBTB2):c.1565T>A (p.Val522Glu)not specified [RCV004350761]uncertain significance134849020248490202Humanname
405682429CV3319333single nucleotide variantNM_001268.4(RCBTB2):c.1148C>T (p.Ser383Leu)not specified [RCV004443601]uncertain significance134850183848501838Humanname
405682438CV3319335single nucleotide variantNM_001268.4(RCBTB2):c.1259G>A (p.Arg420His)not specified [RCV004443603]uncertain significance134849974648499746Humanname
407532159CV3465138single nucleotide variantNM_001268.4(RCBTB2):c.1202A>T (p.Asp401Val)not specified [RCV004657968]uncertain significance134850178448501784Humanname
407532161CV3465139single nucleotide variantNM_001268.4(RCBTB2):c.1258C>T (p.Arg420Cys)not specified [RCV004657969]uncertain significance134849974748499747Humanname
597764450CV3582854single nucleotide variantNM_001268.4(RCBTB2):c.1508A>G (p.Asp503Gly)not specified [RCV004849782]uncertain significance134849619848496198Humanname
597764462CV3582857single nucleotide variantNM_001268.4(RCBTB2):c.1465G>A (p.Glu489Lys)not specified [RCV004849785]uncertain significance134849624148496241Humanname
598255252CV3898987single nucleotide variantNM_001268.4(RCBTB2):c.1636G>A (p.Val546Ile)not specified [RCV005259858]uncertain significance134849013148490131Humanname
598255259CV3898988single nucleotide variantNM_001268.4(RCBTB2):c.1238A>G (p.Lys413Arg)not specified [RCV005259859]uncertain significance134850174848501748Humanname
598255265CV3898989single nucleotide variantNM_001268.4(RCBTB2):c.1247G>A (p.Cys416Tyr)not specified [RCV005259860]uncertain significance134849975848499758Humanname
598255282CV3898992single nucleotide variantNM_001268.4(RCBTB2):c.1279G>A (p.Glu427Lys)not specified [RCV005259863]uncertain significance134849972648499726Humanname