ClinVar Miner

List of variants in gene SNTA1 reported as uncertain significance by Illumina Laboratory Services, Illumina

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Total variants: 31
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HGVS dbSNP gnomAD frequency
NM_003098.3(SNTA1):c.828G>A (p.Lys276=) rs35938843 0.00969
NM_003098.3(SNTA1):c.993C>T (p.Arg331=) rs143309917 0.00125
NM_003098.3(SNTA1):c.984C>T (p.Pro328=) rs138863915 0.00121
NM_003098.3(SNTA1):c.787G>T (p.Ala263Ser) rs150576530 0.00054
NM_003098.3(SNTA1):c.*79C>A rs78892511 0.00040
NM_003098.3(SNTA1):c.210G>C (p.Pro70=) rs751651742 0.00039
NM_003098.3(SNTA1):c.566C>T (p.Ser189Leu) rs144860423 0.00020
NM_003098.3(SNTA1):c.*231C>T rs187657721 0.00018
NM_003098.3(SNTA1):c.1442C>T (p.Ser481Leu) rs370531842 0.00007
NM_003098.3(SNTA1):c.*132C>T rs757013849 0.00006
NM_003098.3(SNTA1):c.1238-14T>C rs369876616 0.00006
NM_003098.3(SNTA1):c.992G>A (p.Arg331His) rs575431717 0.00004
NM_003098.3(SNTA1):c.817C>T (p.Pro273Ser) rs750459988 0.00003
NM_003098.3(SNTA1):c.1118G>A (p.Arg373His) rs754648214 0.00002
NM_003098.3(SNTA1):c.1205G>A (p.Arg402Gln) rs771369802 0.00002
NM_003098.3(SNTA1):c.1479C>T (p.Phe493=) rs559827815 0.00002
NM_003098.3(SNTA1):c.538A>G (p.Thr180Ala) rs747367304 0.00002
NM_003098.3(SNTA1):c.*333G>A rs1222182431 0.00001
NM_003098.3(SNTA1):c.*6G>A rs565582070 0.00001
NM_003098.3(SNTA1):c.1181G>A (p.Arg394His) rs750278583 0.00001
NM_003098.3(SNTA1):c.1256G>A (p.Arg419His) rs751302839 0.00001
NM_003098.3(SNTA1):c.1504G>A (p.Gly502Arg) rs768377696 0.00001
NM_003098.3(SNTA1):c.375G>C (p.Gln125His) rs201421292 0.00001
NM_003098.3(SNTA1):c.514G>A (p.Val172Ile) rs775580363 0.00001
NM_003098.3(SNTA1):c.*412G>C rs566401281
NM_003098.3(SNTA1):c.1025C>G (p.Pro342Arg) rs1989758393
NM_003098.3(SNTA1):c.1238-13G>C rs748801869
NM_003098.3(SNTA1):c.312C>A (p.Gly104=) rs533476140
NM_003098.3(SNTA1):c.651G>A (p.Leu217=) rs886056626
NM_003098.3(SNTA1):c.740T>G (p.Leu247Arg) rs1989777102
NM_003098.3(SNTA1):c.816G>T (p.Thr272=) rs371028127

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