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Variants search result for Homo sapiens
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19 records found for search term Grpel1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405772137CV3258976single nucleotide variantNM_025196.4(GRPEL1):c.7G>C (p.Ala3Pro)not specified [RCV004396117]uncertain significance470680267068026Humanname
405772114CV3258972single nucleotide variantNM_025196.4(GRPEL1):c.26C>T (p.Ala9Val)not specified [RCV004396113]uncertain significance470680077068007Humanname
405772145CV3258977single nucleotide variantNM_025196.4(GRPEL1):c.92C>T (p.Thr31Met)not specified [RCV004396118]uncertain significance470641947064194Humanname
329364146CV2460356single nucleotide variantNM_025196.4(GRPEL1):c.119T>C (p.Leu40Pro)not specified [RCV004268674]uncertain significance470641677064167Humanname
329353421CV2469252single nucleotide variantNM_025196.4(GRPEL1):c.232T>C (p.Tyr78His)not specified [RCV004280593]uncertain significance470624607062460Humanname
401891053CV2778618single nucleotide variantNM_025196.4(GRPEL1):c.149A>G (p.Lys50Arg)not specified [RCV004344265]uncertain significance470641377064137Humanname
405772109CV3258971single nucleotide variantNM_025196.4(GRPEL1):c.265C>T (p.Arg89Trp)not specified [RCV004396112]uncertain significance470624277062427Humanname
407463855CV3433376single nucleotide variantNM_025196.4(GRPEL1):c.182T>C (p.Leu61Pro)not specified [RCV004634934]uncertain significance470641047064104Humanname
156232495CV2227687single nucleotide variantNM_025196.4(GRPEL1):c.453C>G (p.Ile151Met)not specified [RCV004094078]uncertain significance470610637061063Humanname
156047969CV2244987single nucleotide variantNM_025196.4(GRPEL1):c.365C>A (p.Thr122Lys)not specified [RCV004104721]uncertain significance470611517061151Humanname
156074326CV2281431single nucleotide variantNM_025196.4(GRPEL1):c.590T>C (p.Val197Ala)not specified [RCV004153762]uncertain significance470609267060926Humanname
155990222CV2374678single nucleotide variantNM_025196.4(GRPEL1):c.397G>A (p.Asp133Asn)not specified [RCV004225293]uncertain significance470611197061119Humanname
401733699CV2713184single nucleotide variantNM_025196.4(GRPEL1):c.422A>G (p.Tyr141Cys)not specified [RCV004316726]uncertain significance470610947061094Humanname
401927899CV2822397single nucleotide variantNM_025196.4(GRPEL1):c.349G>A (p.Val117Ile)not provided [RCV003439239]likely benign470611677061167Humanname
405772121CV3258973single nucleotide variantNM_025196.4(GRPEL1):c.372T>G (p.Cys124Trp)not specified [RCV004396114]uncertain significance470611447061144Humanname
405772132CV3258975single nucleotide variantNM_025196.4(GRPEL1):c.404C>G (p.Pro135Arg)not specified [RCV004396116]uncertain significance470611127061112Humanname
407463851CV3433375single nucleotide variantNM_025196.4(GRPEL1):c.406C>T (p.His136Tyr)not specified [RCV004634933]uncertain significance470611107061110Humanname
597771675CV3678903single nucleotide variantNM_025196.4(GRPEL1):c.365C>T (p.Thr122Ile)not specified [RCV004928423]uncertain significance470611517061151Humanname
597756145CV3678904single nucleotide variantNM_025196.4(GRPEL1):c.608G>A (p.Gly203Glu)not specified [RCV004924802]uncertain significance470609087060908Humanname