ClinVar Miner

List of variants in gene DSC2 reported as uncertain significance by Color

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Total variants: 26
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HGVS dbSNP
NM_024422.3(DSC2):c.1081G>A (p.Val361Met) rs751810874
NM_024422.3(DSC2):c.1707C>A (p.Asp569Glu) rs201517977
NM_024422.3(DSC2):c.2138C>T (p.Thr713Met) rs180863872
NM_024422.3(DSC2):c.2344G>A (p.Glu782Lys) rs866805043
NM_024422.4(DSC2):c.1766T>C (p.Met589Thr) rs201856473
NM_024422.4(DSC2):c.2335G>A (p.Gly779Arg) rs139290300
NM_024422.4(DSC2):c.2587G>A (p.Gly863Arg) rs147109895
NM_024422.4(DSC2):c.327A>G (p.Ile109Met) rs373305929
NM_024422.4(DSC2):c.408A>G (p.Arg136=) rs561653481
NM_024422.4(DSC2):c.802A>G (p.Thr268Ala) rs201015785
NM_024422.5(DSC2):c.1037A>T (p.Asp346Val)
NM_024422.5(DSC2):c.1157C>G (p.Thr386Ser)
NM_024422.5(DSC2):c.1343G>A (p.Ser448Asn)
NM_024422.5(DSC2):c.1750A>G (p.Ile584Val)
NM_024422.5(DSC2):c.1907C>G (p.Ser636Cys)
NM_024422.5(DSC2):c.2020G>A (p.Glu674Lys)
NM_024422.5(DSC2):c.2035C>T (p.His679Tyr)
NM_024422.5(DSC2):c.2229A>C (p.Glu743Asp)
NM_024422.5(DSC2):c.2318G>T (p.Gly773Val)
NM_024422.5(DSC2):c.2392C>T (p.Arg798Trp)
NM_024422.5(DSC2):c.286A>G (p.Ile96Val) rs772447450
NM_024422.5(DSC2):c.393G>T (p.Arg131Ser)
NM_024422.5(DSC2):c.548G>A (p.Arg183Gln) rs554713834
NM_024422.5(DSC2):c.664A>G (p.Thr222Ala)
NM_024422.5(DSC2):c.740C>A (p.Thr247Asn)
NM_024422.5(DSC2):c.906C>T (p.Gly302=)

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