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Variants search result for Homo sapiens
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22 records found for search term Sult1b1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401726679CV2738275single nucleotide variantNM_014465.4(SULT1B1):c.376-6044T>CLevothyroxine response [RCV003317016]other46974030869740308Humanname
329389215CV2467194single nucleotide variantNM_014465.4(SULT1B1):c.10C>T (p.Pro4Ser)not specified [RCV004285011]uncertain significance46975520869755208Humanname
15160338CV709432single nucleotide variantNM_014465.4(SULT1B1):c.192T>C (p.Asp64=)not provided [RCV000969882]benign46975475569754755Humanname
407530202CV3481864single nucleotide variantNM_014465.4(SULT1B1):c.78C>A (p.Ser26Arg)not specified [RCV004681747]uncertain significance46975514069755140Humanname
405705294CV3327400single nucleotide variantNM_014465.4(SULT1B1):c.272C>T (p.Thr91Ile)not specified [RCV004460992]likely benign46975467569754675Humanname
407497233CV3481865single nucleotide variantNM_014465.4(SULT1B1):c.286C>A (p.Gln96Lys)not specified [RCV004668335]uncertain significance46974981069749810Humanname
407497237CV3481867single nucleotide variantNM_014465.4(SULT1B1):c.278G>A (p.Gly93Asp)not specified [RCV004668336]uncertain significance46974981869749818Humanname
156297678CV2246900single nucleotide variantNM_014465.4(SULT1B1):c.628A>G (p.Arg210Gly)not specified [RCV004112702]uncertain significance46973065169730651Humanname
156174362CV2334529single nucleotide variantNM_014465.4(SULT1B1):c.665A>G (p.Asp222Gly)not specified [RCV004188490]uncertain significance46973061469730614Humanname
401723551CV2724943single nucleotide variantNM_014465.4(SULT1B1):c.569T>A (p.Leu190His)not specified [RCV004319707]uncertain significance46973344169733441Humanname
401869808CV2792187single nucleotide variantNM_014465.4(SULT1B1):c.392G>C (p.Arg131Pro)not specified [RCV004361394]uncertain significance46973424869734248Humanname
401923314CV2822555single nucleotide variantNM_014465.4(SULT1B1):c.782C>T (p.Thr261Met)not provided [RCV003435029]likely benign46972719769727197Humanname
405705302CV3327401single nucleotide variantNM_014465.4(SULT1B1):c.836C>T (p.Ala279Val)not specified [RCV004460993]uncertain significance46972714369727143Humanname
405705717CV3327402single nucleotide variantNM_014465.4(SULT1B1):c.838A>G (p.Ile280Val)not specified [RCV004460994]uncertain significance46972714169727141Humanname
405705722CV3327403single nucleotide variantNM_014465.4(SULT1B1):c.877C>T (p.Arg293Cys)not specified [RCV004460995]uncertain significance46972710269727102Humanname
407530203CV3481866single nucleotide variantNM_014465.4(SULT1B1):c.848C>T (p.Thr283Ile)not specified [RCV004681748]uncertain significance46972713169727131Humanname
597759654CV3611999single nucleotide variantNM_014465.4(SULT1B1):c.657G>C (p.Glu219Asp)not specified [RCV004869030]uncertain significance46973062269730622Humanname
597759658CV3612000single nucleotide variantNM_014465.4(SULT1B1):c.315T>G (p.Ile105Met)not specified [RCV004869031]uncertain significance46974978169749781Humanname
597759663CV3612001single nucleotide variantNM_014465.4(SULT1B1):c.630A>T (p.Arg210Ser)not specified [RCV004869032]uncertain significance46973064969730649Humanname
597759666CV3612002single nucleotide variantNM_014465.4(SULT1B1):c.677A>G (p.His226Arg)not specified [RCV004869033]uncertain significance46973060269730602Humanname
598221681CV3912441single nucleotide variantNM_014465.4(SULT1B1):c.569T>C (p.Leu190Pro)not specified [RCV005293658]uncertain significance46973344169733441Humanname
15196542CV698610single nucleotide variantNM_014465.4(SULT1B1):c.433T>G (p.Leu145Val)not provided [RCV000956218]benign46973420769734207Humanname