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16 records found for search term Lrrc3b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598273070CV3984684single nucleotide variantNM_052953.4(LRRC3B):c.24A>C (p.Leu8Phe)not specified [RCV005350624]uncertain significance32670969626709696Humanname
598251001CV3984685single nucleotide variantNM_052953.4(LRRC3B):c.25A>C (p.Thr9Pro)not specified [RCV005366606]uncertain significance32670969726709697Humanname
8625598CV80722single nucleotide variantNM_052953.2(LRRC3B):c.240C>T (p.Pro80=)Malignant melanoma [RCV000060799]not provided32670991226709912Humanname
156007184CV2357863single nucleotide variantNM_052953.4(LRRC3B):c.28C>G (p.Arg10Gly)not specified [RCV004205144]uncertain significance32670970026709700Humanname
401752390CV2723219single nucleotide variantNM_052953.4(LRRC3B):c.56A>G (p.Gln19Arg)not specified [RCV004329455]uncertain significance32670972826709728Humanname
597778572CV3693390single nucleotide variantNM_052953.4(LRRC3B):c.41T>C (p.Met14Thr)not specified [RCV004930164]uncertain significance32670971326709713Humanname
15189654CV698018single nucleotide variantNM_052953.4(LRRC3B):c.573C>T (p.Asp191=)not provided [RCV000954244]benign32671024526710245Humanname
156297215CV2297655single nucleotide variantNM_052953.4(LRRC3B):c.179G>A (p.Arg60Lys)not specified [RCV004155342]uncertain significance32670985126709851Humanname
597626185CV3693389single nucleotide variantNM_052953.4(LRRC3B):c.155A>G (p.Asn52Ser)not specified [RCV004938555]uncertain significance32670982726709827Humanname
156241471CV2246110single nucleotide variantNM_052953.4(LRRC3B):c.574G>A (p.Ala192Thr)not specified [RCV004114014]uncertain significance32671024626710246Humanname
156111200CV2261714single nucleotide variantNM_052953.4(LRRC3B):c.664G>T (p.Val222Leu)not specified [RCV004126015]uncertain significance32671033626710336Humanname
156151746CV2268974single nucleotide variantNM_052953.4(LRRC3B):c.658T>C (p.Tyr220His)not specified [RCV004128375]uncertain significance32671033026710330Humanname
405655797CV3277398single nucleotide variantNM_052953.4(LRRC3B):c.642C>A (p.Phe214Leu)not specified [RCV004415551]uncertain significance32671031426710314Humanname
598250996CV3984683single nucleotide variantNM_052953.4(LRRC3B):c.644C>T (p.Thr215Ile)not specified [RCV005366605]uncertain significance32671031626710316Humanname
598251008CV3984686single nucleotide variantNM_052953.4(LRRC3B):c.752A>G (p.Glu251Gly)not specified [RCV005366607]uncertain significance32671042426710424Humanname
598222302CV3984687single nucleotide variantNM_052953.4(LRRC3B):c.327A>C (p.Lys109Asn)not specified [RCV005379871]uncertain significance32670999926709999Humanname