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Variants search result for Homo sapiens
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32 records found for search term Tfb1m
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8581662CV116107single nucleotide variantNM_016020.3(TFB1M):c.547-4362A>GLung cancer [RCV000096630]uncertain significance6155289639155289639Humanname
155922467CV2207504single nucleotide variantNM_016020.4(TFB1M):c.19C>T (p.Leu7Phe)not specified [RCV004089976]uncertain significance6155314410155314410Humanname
401879424CV2755090single nucleotide variantNM_016020.4(TFB1M):c.10T>C (p.Ser4Pro)not specified [RCV004335243]likely benign6155314419155314419Humanname
15166676CV721836single nucleotide variantNM_016020.4(TFB1M):c.180C>T (p.Tyr60=)not provided [RCV000882682]benign6155311293155311293Humanname
329397567CV2463861single nucleotide variantNM_016020.4(TFB1M):c.290T>G (p.Leu97Arg)not specified [RCV004279939]uncertain significance6155298581155298581Humanname
401736377CV2689327single nucleotide variantNM_016020.4(TFB1M):c.170C>T (p.Ala57Val)not specified [RCV004306152]uncertain significance6155311303155311303Humanname
401737616CV2695846single nucleotide variantNM_016020.4(TFB1M):c.213A>T (p.Arg71Ser)not specified [RCV004308128]uncertain significance6155311260155311260Humanname
597751433CV3619843single nucleotide variantNM_016020.4(TFB1M):c.105G>C (p.Gln35His)not specified [RCV004866925]uncertain significance6155314324155314324Humanname
597751437CV3619845single nucleotide variantNM_016020.4(TFB1M):c.202G>A (p.Gly68Arg)not specified [RCV004866927]uncertain significance6155311271155311271Humanname
8626120CV81264single nucleotide variantNM_016020.3(TFB1M):c.112C>T (p.Leu38Phe)Malignant melanoma [RCV000061342]not provided6155314317155314317Humanname
155927641CV2285205single nucleotide variantNM_016020.4(TFB1M):c.595A>G (p.Met199Val)not specified [RCV004145412]uncertain significance6155285229155285229Humanname
156005790CV2290401single nucleotide variantNM_016020.4(TFB1M):c.655C>T (p.Pro219Ser)not specified [RCV004154821]uncertain significance6155285169155285169Humanname
156166844CV2330153single nucleotide variantNM_016020.4(TFB1M):c.620G>A (p.Arg207Gln)not specified [RCV004185640]likely benign6155285204155285204Humanname
155919358CV2360235single nucleotide variantNM_016020.4(TFB1M):c.404A>G (p.Asn135Ser)not specified [RCV004208582]uncertain significance6155297095155297095Humanname
156153716CV2395005single nucleotide variantNM_016020.4(TFB1M):c.785G>A (p.Arg262Gln)not specified [RCV004236698]uncertain significance6155260282155260282Humanname
156194260CV2398205single nucleotide variantNM_016020.4(TFB1M):c.578G>A (p.Arg193His)not specified [RCV004241774]uncertain significance6155285246155285246Humanname
329349529CV2436972single nucleotide variantNM_016020.4(TFB1M):c.935A>G (p.Asp312Gly)not specified [RCV004260343]uncertain significance6155257942155257942Humanname
329401857CV2457947single nucleotide variantNM_016020.4(TFB1M):c.424C>A (p.Leu142Met)not specified [RCV004271531]uncertain significance6155297075155297075Humanname
405783322CV3342668single nucleotide variantNM_016020.4(TFB1M):c.322G>A (p.Val108Ile)not specified [RCV004472344]uncertain significance6155298549155298549Humanname
405783327CV3342669single nucleotide variantNM_016020.4(TFB1M):c.817C>T (p.Arg273Cys)not specified [RCV004472345]uncertain significance6155258060155258060Humanname
405783333CV3342670single nucleotide variantNM_016020.4(TFB1M):c.878G>A (p.Arg293His)not specified [RCV004472346]uncertain significance6155257999155257999Humanname
405783340CV3342671single nucleotide variantNM_016020.4(TFB1M):c.916G>A (p.Val306Ile)not specified [RCV004472347]uncertain significance6155257961155257961Humanname
407519945CV3482567single nucleotide variantNM_016020.4(TFB1M):c.398C>T (p.Pro133Leu)not specified [RCV004676768]uncertain significance6155297101155297101Humanname
597688355CV3619841single nucleotide variantNM_016020.4(TFB1M):c.983G>A (p.Arg328Gln)not specified [RCV004866923]likely benign6155257894155257894Humanname
597688365CV3619842single nucleotide variantNM_016020.4(TFB1M):c.906C>G (p.Ser302Arg)not specified [RCV004866924]uncertain significance6155257971155257971Humanname
597688375CV3619844single nucleotide variantNM_016020.4(TFB1M):c.850G>T (p.Ala284Ser)not specified [RCV004866926]uncertain significance6155258027155258027Humanname
598183238CV3917041single nucleotide variantNM_016020.4(TFB1M):c.646G>A (p.Ala216Thr)not specified [RCV005287074]uncertain significance6155285178155285178Humanname
598183251CV3917043single nucleotide variantNM_016020.4(TFB1M):c.623A>G (p.His208Arg)not specified [RCV005287076]uncertain significance6155285201155285201Humanname
598165672CV3917044single nucleotide variantNM_016020.4(TFB1M):c.482G>A (p.Arg161Lys)not specified [RCV005283489]uncertain significance6155297017155297017Humanname
598183258CV3917045single nucleotide variantNM_016020.4(TFB1M):c.836G>A (p.Arg279Lys)not specified [RCV005287077]likely benign6155258041155258041Humanname
598183264CV3917046single nucleotide variantNM_016020.4(TFB1M):c.716A>G (p.Glu239Gly)not specified [RCV005287078]uncertain significance6155260351155260351Humanname
598165678CV3917047single nucleotide variantNM_016020.4(TFB1M):c.889A>G (p.Ile297Val)not specified [RCV005283490]likely benign6155257988155257988Humanname