ClinVar Miner

List of variants in gene NDST1 reported as uncertain significance for not provided

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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_001543.5(NDST1):c.239G>A (p.Arg80His) rs145390254 0.00145
NM_001543.5(NDST1):c.760G>A (p.Ala254Thr) rs146548363 0.00083
NM_001543.5(NDST1):c.334C>T (p.Arg112Cys) rs138962514 0.00036
NM_001543.5(NDST1):c.2405T>C (p.Ile802Thr) rs146304238 0.00010
NM_001543.5(NDST1):c.1690G>C (p.Val564Leu) rs774976739 0.00006
NM_001543.5(NDST1):c.161C>G (p.Pro54Arg) rs140436588 0.00004
NM_001543.5(NDST1):c.169G>A (p.Gly57Arg) rs540715914 0.00004
NM_001543.5(NDST1):c.1736A>G (p.Asp579Gly) rs763682889 0.00004
NM_001543.5(NDST1):c.883G>A (p.Val295Met) rs747017483 0.00001
NM_001543.5(NDST1):c.1008+4T>A
NM_001543.5(NDST1):c.1057A>C (p.Thr353Pro) rs2151285581
NM_001543.5(NDST1):c.141del (p.Ser48fs)
NM_001543.5(NDST1):c.1432A>G (p.Ile478Val) rs373125426
NM_001543.5(NDST1):c.1666C>G (p.Leu556Val)
NM_001543.5(NDST1):c.1690G>A (p.Val564Met) rs774976739
NM_001543.5(NDST1):c.1726GAG[1] (p.Glu577del) rs757264097
NM_001543.5(NDST1):c.1850C>T (p.Thr617Ile)
NM_001543.5(NDST1):c.188C>T (p.Ala63Val) rs764353194
NM_001543.5(NDST1):c.1951T>C (p.Tyr651His)
NM_001543.5(NDST1):c.197G>A (p.Arg66His)
NM_001543.5(NDST1):c.2060C>T (p.Pro687Leu) rs940152063
NM_001543.5(NDST1):c.2062C>T (p.Arg688Trp)
NM_001543.5(NDST1):c.2090C>T (p.Ala697Val)
NM_001543.5(NDST1):c.2206G>A (p.Ala736Thr)
NM_001543.5(NDST1):c.2225C>T (p.Ser742Leu)
NM_001543.5(NDST1):c.227C>T (p.Ala76Val)
NM_001543.5(NDST1):c.2287C>T (p.Arg763Cys)
NM_001543.5(NDST1):c.2345G>A (p.Arg782His)
NM_001543.5(NDST1):c.2371A>G (p.Met791Val)
NM_001543.5(NDST1):c.23G>A (p.Arg8Gln)
NM_001543.5(NDST1):c.2426C>T (p.Ala809Val)
NM_001543.5(NDST1):c.2457A>C (p.Gln819His)
NM_001543.5(NDST1):c.281C>T (p.Ser94Leu)
NM_001543.5(NDST1):c.347C>T (p.Ala116Val)
NM_001543.5(NDST1):c.39C>G (p.His13Gln) rs777877507
NM_001543.5(NDST1):c.765C>A (p.Asp255Glu)
NM_001543.5(NDST1):c.766G>A (p.Ala256Thr)
NM_001543.5(NDST1):c.905C>T (p.Thr302Met)
NM_001543.5(NDST1):c.914G>A (p.Arg305His)
NM_001543.5(NDST1):c.950A>T (p.Asp317Val)
NM_001543.5(NDST1):c.967G>A (p.Val323Met)

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