ClinVar Miner

List of variants in gene SNTA1 reported as likely benign by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP gnomAD frequency
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.221C>T (p.Pro74Leu) rs572545726 0.00198
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.1488C>A (p.Ala496=) rs34901081 0.00106
NM_003098.3(SNTA1):c.440C>A (p.Thr147Asn) rs141724500 0.00067
NM_003098.3(SNTA1):c.787G>T (p.Ala263Ser) rs150576530 0.00054
NM_003098.3(SNTA1):c.619C>T (p.Arg207Trp) rs139537086 0.00044
NM_003098.3(SNTA1):c.784A>C (p.Thr262Pro) rs200316080 0.00041
NM_003098.3(SNTA1):c.210G>C (p.Pro70=) rs751651742 0.00039
NM_003098.3(SNTA1):c.677G>A (p.Cys226Tyr) rs34479952 0.00037
NM_003098.3(SNTA1):c.566C>T (p.Ser189Leu) rs144860423 0.00020
NM_003098.3(SNTA1):c.1088A>C (p.Glu363Ala) rs147964932 0.00017
NM_003098.3(SNTA1):c.430T>G (p.Ser144Ala) rs142978180 0.00017
NM_003098.3(SNTA1):c.1032C>T (p.Ile344=) rs541665582 0.00015
NM_003098.3(SNTA1):c.815C>T (p.Thr272Met) rs144465646 0.00011
NM_003098.3(SNTA1):c.1377C>T (p.Asp459=) rs146134721 0.00009
NM_003098.3(SNTA1):c.589C>T (p.Arg197Trp) rs530603992 0.00006
NM_003098.3(SNTA1):c.339C>G (p.Leu113=) rs746780665 0.00004
NM_003098.3(SNTA1):c.447T>C (p.Asp149=) rs760527177 0.00004
NM_003098.3(SNTA1):c.513C>T (p.Asp171=) rs182320044 0.00004
NM_003098.3(SNTA1):c.820C>T (p.Arg274Trp) rs201763667 0.00004
NM_003098.3(SNTA1):c.910C>T (p.Leu304=) rs141775350 0.00004
NM_003098.3(SNTA1):c.1309G>A (p.Glu437Lys) rs371648806 0.00003
NM_003098.3(SNTA1):c.160G>C (p.Gly54Arg) rs786205848 0.00003
NM_003098.3(SNTA1):c.1209C>T (p.Ala403=) rs144821472 0.00002
NM_003098.3(SNTA1):c.1440C>T (p.His480=) rs201485963 0.00002
NM_003098.3(SNTA1):c.522G>A (p.Pro174=) rs780808390 0.00002
NM_003098.3(SNTA1):c.620G>A (p.Arg207Gln) rs771180054 0.00002
NM_003098.3(SNTA1):c.972C>T (p.Tyr324=) rs761467167 0.00002
NM_003098.3(SNTA1):c.1006C>T (p.Arg336Trp) rs747104878 0.00001
NM_003098.3(SNTA1):c.1104G>A (p.Leu368=) rs758435546 0.00001
NM_003098.3(SNTA1):c.1230G>A (p.Val410=) rs142580715 0.00001
NM_003098.3(SNTA1):c.1245G>A (p.Thr415=) rs780680201 0.00001
NM_003098.3(SNTA1):c.1359G>A (p.Leu453=) rs760768761 0.00001
NM_003098.3(SNTA1):c.1386T>C (p.Ser462=) rs1335638175 0.00001
NM_003098.3(SNTA1):c.1485G>A (p.Ser495=) rs374100952 0.00001
NM_003098.3(SNTA1):c.173A>G (p.Glu58Gly) rs555231776 0.00001
NM_003098.3(SNTA1):c.526T>C (p.Phe176Leu) rs781703999 0.00001
NM_003098.3(SNTA1):c.630C>T (p.Ser210=) rs747390007 0.00001
NM_003098.3(SNTA1):c.837G>A (p.Leu279=) rs746607636 0.00001
NM_003098.3(SNTA1):c.1050C>T (p.His350=)
NM_003098.3(SNTA1):c.1122C>T (p.His374=)
NM_003098.3(SNTA1):c.1182C>A (p.Arg394=)
NM_003098.3(SNTA1):c.1278C>T (p.His426=)
NM_003098.3(SNTA1):c.1305G>A (p.Ala435=)
NM_003098.3(SNTA1):c.1335C>T (p.Leu445=)
NM_003098.3(SNTA1):c.1353G>A (p.Glu451=)
NM_003098.3(SNTA1):c.1396C>T (p.Leu466=)
NM_003098.3(SNTA1):c.1517_*2dup (p.Ter506=)
NM_003098.3(SNTA1):c.159C>T (p.Pro53=)
NM_003098.3(SNTA1):c.162C>G (p.Gly54=)
NM_003098.3(SNTA1):c.168G>T (p.Pro56=)
NM_003098.3(SNTA1):c.201C>G (p.Ala67=)
NM_003098.3(SNTA1):c.213C>G (p.Gly71=) rs1374381593
NM_003098.3(SNTA1):c.216C>A (p.Ala72=)
NM_003098.3(SNTA1):c.219G>C (p.Gly73=) rs764093818
NM_003098.3(SNTA1):c.222C>T (p.Pro74=)
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.312C>A (p.Gly104=) rs533476140
NM_003098.3(SNTA1):c.312C>T (p.Gly104=) rs533476140
NM_003098.3(SNTA1):c.361T>C (p.Leu121=)
NM_003098.3(SNTA1):c.453G>A (p.Ala151=) rs949573711
NM_003098.3(SNTA1):c.456G>A (p.Val152=)
NM_003098.3(SNTA1):c.540T>C (p.Thr180=) rs1600844808
NM_003098.3(SNTA1):c.567A>C (p.Ser189=) rs552315106
NM_003098.3(SNTA1):c.567A>T (p.Ser189=) rs552315106
NM_003098.3(SNTA1):c.669G>A (p.Ser223=) rs199762207
NM_003098.3(SNTA1):c.699C>T (p.Pro233=)
NM_003098.3(SNTA1):c.717C>T (p.Cys239=)
NM_003098.3(SNTA1):c.725A>G (p.Asp242Gly)
NM_003098.3(SNTA1):c.735C>T (p.Asp245=)
NM_003098.3(SNTA1):c.768T>C (p.Ser256=)
NM_003098.3(SNTA1):c.777G>A (p.Ser259=)
NM_003098.3(SNTA1):c.819G>A (p.Pro273=)
NM_003098.3(SNTA1):c.885G>A (p.Lys295=)
NM_003098.3(SNTA1):c.891T>A (p.Ile297=)
NM_003098.3(SNTA1):c.933C>T (p.Pro311=)
NM_003098.3(SNTA1):c.974T>C (p.Leu325Ser)

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