ClinVar Miner

List of variants in gene SNTA1 reported as likely benign for not specified

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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_003098.3(SNTA1):c.221C>T (p.Pro74Leu) rs572545726 0.00198
NM_003098.3(SNTA1):c.784A>C (p.Thr262Pro) rs200316080 0.00041
NM_003098.3(SNTA1):c.1088A>C (p.Glu363Ala) rs147964932 0.00017
NM_003098.3(SNTA1):c.1425+18del rs746145193 0.00012
NM_003098.3(SNTA1):c.815C>T (p.Thr272Met) rs144465646 0.00011
NM_003098.3(SNTA1):c.1442C>T (p.Ser481Leu) rs370531842 0.00007
NM_003098.3(SNTA1):c.1158G>A (p.Pro386=) rs774320273 0.00004
NM_003098.3(SNTA1):c.339C>G (p.Leu113=) rs746780665 0.00004
NM_003098.3(SNTA1):c.910C>T (p.Leu304=) rs141775350 0.00004
NM_003098.3(SNTA1):c.310+19G>A rs554224001 0.00003
NM_003098.3(SNTA1):c.701+6G>A rs763906288 0.00002
NM_003098.3(SNTA1):c.702-7C>G rs780688953 0.00002
NM_003098.3(SNTA1):c.*14C>T rs761196972 0.00001
NM_003098.3(SNTA1):c.173A>G (p.Glu58Gly) rs555231776 0.00001
NM_003098.3(SNTA1):c.630C>T (p.Ser210=) rs747390007 0.00001
NM_003098.3(SNTA1):c.1480C>T (p.Leu494=) rs763351253
NM_003098.3(SNTA1):c.219G>C (p.Gly73=) rs764093818
NM_003098.3(SNTA1):c.229C>T (p.Leu77=) rs886038523
NM_003098.3(SNTA1):c.240G>A (p.Ala80=) rs765352601
NM_003098.3(SNTA1):c.310+12_310+27del rs1441274981
NM_003098.3(SNTA1):c.311-6G>A rs139532210
NM_003098.3(SNTA1):c.846G>A (p.Leu282=) rs778688832
NM_003098.3(SNTA1):c.910-10T>A rs1555817114

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