ClinVar Miner

List of variants in gene SNTA1 studied for not specified

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Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_003098.3(SNTA1):c.807T>C (p.Asn269=) rs73270015 0.02196
NM_003098.3(SNTA1):c.1350C>T (p.Phe450=) rs116747979 0.01203
NM_003098.3(SNTA1):c.555C>T (p.Val185=) rs34995247 0.00948
NM_003098.3(SNTA1):c.317G>A (p.Arg106Gln) rs75025585 0.00904
NM_003098.3(SNTA1):c.166C>T (p.Pro56Ser) rs573772189 0.00585
NM_003098.3(SNTA1):c.701+10G>A rs6057846 0.00419
NM_003098.3(SNTA1):c.1426-5T>C rs183939417 0.00221
NM_003098.3(SNTA1):c.770C>G (p.Ala257Gly) rs56157422 0.00217
NM_003098.3(SNTA1):c.311-6G>C rs139532210 0.00201
NM_003098.3(SNTA1):c.221C>T (p.Pro74Leu) rs572545726 0.00198
NM_003098.3(SNTA1):c.984C>T (p.Pro328=) rs138863915 0.00121
NM_003098.3(SNTA1):c.497-7C>T rs116972153 0.00063
NM_003098.3(SNTA1):c.787G>T (p.Ala263Ser) rs150576530 0.00054
NM_003098.3(SNTA1):c.784A>C (p.Thr262Pro) rs200316080 0.00041
NM_003098.3(SNTA1):c.677G>A (p.Cys226Tyr) rs34479952 0.00037
NM_003098.3(SNTA1):c.909+17G>T rs376695170 0.00021
NM_003098.3(SNTA1):c.1088A>C (p.Glu363Ala) rs147964932 0.00017
NM_003098.3(SNTA1):c.311-20C>T rs200764326 0.00013
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.452C>T (p.Ala151Val) rs772936861 0.00004
NM_003098.3(SNTA1):c.910C>T (p.Leu304=) rs141775350 0.00004
NM_003098.3(SNTA1):c.1238-11C>T rs779500941 0.00003
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.1339C>T (p.Arg447Ter) rs1187536758 0.00001
NM_003098.3(SNTA1):c.1425+1G>A rs113809208 0.00001
NM_003098.3(SNTA1):c.1425C>T (p.Ile475=) rs775932782 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.759T>A (p.Asp253Glu) rs759487225 0.00001
NM_003098.3(SNTA1):c.1480C>T (p.Leu494=) rs763351253
NM_003098.3(SNTA1):c.1498del (p.Arg500fs) rs1568745571
NM_003098.3(SNTA1):c.205G>A (p.Glu69Lys) rs1555822126
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.567A>T (p.Ser189=) rs552315106
NM_003098.3(SNTA1):c.846G>A (p.Leu282=) rs778688832
NM_003098.3(SNTA1):c.910-10T>A rs1555817114

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