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Variants search result for Homo sapiens
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21 records found for search term Reg1a
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15202276CV747789single nucleotide variantNM_002909.5(REG1A):c.30G>C (p.Leu10=)not provided [RCV000913382]benign27912089179120891Humanname
155645533CV1710891single nucleotide variantNM_002909.5(REG1A):c.168C>T (p.Thr56=)Kidney disorder [RCV002294672]likely benign27912166579121665Human2name
598204107CV3909279single nucleotide variantNM_002909.5(REG1A):c.13A>G (p.Ser5Gly)not specified [RCV005269487]likely benign27912087479120874Humanname
155645519CV1710881single nucleotide variantNM_002909.5(REG1A):c.80C>G (p.Thr27Arg)Focal segmental glomerulosclerosis [RCV002294662]uncertain significance27912157779121577Human2name
405683213CV3315640single nucleotide variantNM_002909.5(REG1A):c.57G>C (p.Gln19His)not specified [RCV004443797]uncertain significance27912091879120918Humanname
597765021CV3583227single nucleotide variantNM_002909.5(REG1A):c.55C>G (p.Gln19Glu)not specified [RCV004849926]uncertain significance27912091679120916Humanname
597765025CV3583228single nucleotide variantNM_002909.5(REG1A):c.56A>G (p.Gln19Arg)not specified [RCV004849927]uncertain significance27912091779120917Humanname
598204113CV3909280single nucleotide variantNM_002909.5(REG1A):c.67C>G (p.Gln23Glu)not specified [RCV005269488]likely benign27912156479121564Humanname
598204119CV3909281single nucleotide variantNM_002909.5(REG1A):c.72G>T (p.Glu24Asp)not specified [RCV005269489]uncertain significance27912156979121569Humanname
15202007CV719974single nucleotide variantNM_002909.5(REG1A):c.450G>A (p.Lys150=)not provided [RCV000891356]benign27912316479123164Humanname
401864353CV2777804single nucleotide variantNM_002909.5(REG1A):c.172G>A (p.Val58Ile)not specified [RCV004345993]uncertain significance27912166979121669Humanname
407532296CV3465283single nucleotide variantNM_002909.5(REG1A):c.137A>G (p.Tyr46Cys)not specified [RCV004658067]uncertain significance27912163479121634Humanname
8630455CV85610single nucleotide variantNM_002909.4(REG1A):c.203A>T (p.Asn68Ile)Malignant melanoma [RCV000065693]not provided27912200779122007Humanname
8630456CV85611single nucleotide variantNM_002909.4(REG1A):c.206C>T (p.Ser69Leu)Malignant melanoma [RCV000065694]not provided27912201079122010Humanname
8630457CV85612single nucleotide variantNM_002909.4(REG1A):c.221C>T (p.Ser74Phe)Malignant melanoma [RCV000065695]not provided27912202579122025Humanname
156226219CV2352723single nucleotide variantNM_002909.5(REG1A):c.389G>A (p.Ser130Asn)not specified [RCV004198746]likely benign27912290879122908Humanname
156039494CV2384270single nucleotide variantNM_002909.5(REG1A):c.325C>T (p.Arg109Cys)not specified [RCV004227657]uncertain significance27912284479122844Humanname
401743417CV2684699single nucleotide variantNM_002909.5(REG1A):c.449A>G (p.Lys150Arg)not specified [RCV004293791]uncertain significance27912316379123163Humanname
405683206CV3315638single nucleotide variantNM_002909.5(REG1A):c.300T>G (p.Ile100Met)not specified [RCV004443795]uncertain significance27912210479122104Humanname
405683210CV3315639single nucleotide variantNM_002909.5(REG1A):c.388A>G (p.Ser130Gly)not specified [RCV004443796]uncertain significance27912290779122907Humanname
8630458CV85613single nucleotide variantNM_002909.4(REG1A):c.425C>T (p.Ser142Leu)Malignant melanoma [RCV000065696]not provided27912294479122944Humanname