List of variants in gene SNTA1 reported as likely benign for Long QT syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 101

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HGVS	dbSNP	gnomAD frequency
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.440C>A (p.Thr147Asn)	rs141724500	0.00067
NM_003098.3(SNTA1):c.619C>T (p.Arg207Trp)	rs139537086	0.00044
NM_003098.3(SNTA1):c.210G>C (p.Pro70=)	rs751651742	0.00039
NM_003098.3(SNTA1):c.1080C>T (p.Tyr360=)	rs141844806	0.00019
NM_003098.3(SNTA1):c.1032C>T (p.Ile344=)	rs541665582	0.00015
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.1377C>T (p.Asp459=)	rs146134721	0.00009
NM_003098.3(SNTA1):c.1238-14T>C	rs369876616	0.00006
NM_003098.3(SNTA1):c.1281C>T (p.Ile427=)	rs761116006	0.00006
NM_003098.3(SNTA1):c.589C>T (p.Arg197Trp)	rs530603992	0.00006
NM_003098.3(SNTA1):c.162C>T (p.Gly54=)	rs544127915	0.00005
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.447T>C (p.Asp149=)	rs760527177	0.00004
NM_003098.3(SNTA1):c.513C>T (p.Asp171=)	rs182320044	0.00004
NM_003098.3(SNTA1):c.847T>C (p.Leu283=)	rs754862058	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.1209C>T (p.Ala403=)	rs144821472	0.00002
NM_003098.3(SNTA1):c.1212C>T (p.Ala404=)	rs754521867	0.00002
NM_003098.3(SNTA1):c.1440C>T (p.His480=)	rs201485963	0.00002
NM_003098.3(SNTA1):c.1479C>T (p.Phe493=)	rs559827815	0.00002
NM_003098.3(SNTA1):c.522G>A (p.Pro174=)	rs780808390	0.00002
NM_003098.3(SNTA1):c.702-7C>G	rs780688953	0.00002
NM_003098.3(SNTA1):c.1104G>A (p.Leu368=)	rs758435546	0.00001
NM_003098.3(SNTA1):c.1245G>A (p.Thr415=)	rs780680201	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.198C>A (p.Gly66=)	rs1335292078	0.00001
NM_003098.3(SNTA1):c.354C>T (p.Phe118=)	rs1178809115	0.00001
NM_003098.3(SNTA1):c.441C>T (p.Thr147=)	rs1421000101	0.00001
NM_003098.3(SNTA1):c.630C>T (p.Ser210=)	rs747390007	0.00001
NM_003098.3(SNTA1):c.816G>A (p.Thr272=)	rs371028127	0.00001
NM_003098.3(SNTA1):c.837G>A (p.Leu279=)	rs746607636	0.00001
NM_003098.3(SNTA1):c.1038C>T (p.Thr346=)	rs763466091
NM_003098.3(SNTA1):c.1040+11G>A
NM_003098.3(SNTA1):c.1041-11C>G
NM_003098.3(SNTA1):c.1047G>A (p.Val349=)	rs954667824
NM_003098.3(SNTA1):c.1047G>C (p.Val349=)
NM_003098.3(SNTA1):c.1053A>G (p.Ser351=)	rs1555816772
NM_003098.3(SNTA1):c.1122C>T (p.His374=)
NM_003098.3(SNTA1):c.1158G>T (p.Pro386=)	rs774320273
NM_003098.3(SNTA1):c.1164G>A (p.Glu388=)
NM_003098.3(SNTA1):c.1191G>C (p.Val397=)	rs1555816721
NM_003098.3(SNTA1):c.1197C>T (p.Gly399=)
NM_003098.3(SNTA1):c.1237+20G>A	rs1989701964
NM_003098.3(SNTA1):c.1238-13G>C	rs748801869
NM_003098.3(SNTA1):c.1238-9dup
NM_003098.3(SNTA1):c.1269G>A (p.Leu423=)
NM_003098.3(SNTA1):c.1338G>A (p.Leu446=)
NM_003098.3(SNTA1):c.1425+15G>A
NM_003098.3(SNTA1):c.1428G>A (p.Gln476=)	rs1060504991
NM_003098.3(SNTA1):c.1443G>A (p.Ser481=)
NM_003098.3(SNTA1):c.1480C>T (p.Leu494=)	rs763351253
NM_003098.3(SNTA1):c.1482G>T (p.Leu494=)
NM_003098.3(SNTA1):c.150T>G (p.Gly50=)
NM_003098.3(SNTA1):c.168G>T (p.Pro56=)
NM_003098.3(SNTA1):c.180G>A (p.Glu60=)
NM_003098.3(SNTA1):c.201C>G (p.Ala67=)
NM_003098.3(SNTA1):c.210G>T (p.Pro70=)	rs751651742
NM_003098.3(SNTA1):c.213C>G (p.Gly71=)	rs1374381593
NM_003098.3(SNTA1):c.222C>G (p.Pro74=)	rs752864338
NM_003098.3(SNTA1):c.225G>A (p.Pro75=)	rs2146814729
NM_003098.3(SNTA1):c.240G>A (p.Ala80=)	rs765352601
NM_003098.3(SNTA1):c.240G>T (p.Ala80=)	rs765352601
NM_003098.3(SNTA1):c.310+10G>C
NM_003098.3(SNTA1):c.310+12_310+27del	rs1441274981
NM_003098.3(SNTA1):c.310+17G>A
NM_003098.3(SNTA1):c.311-16T>G	rs998028927
NM_003098.3(SNTA1):c.311-6G>A	rs139532210
NM_003098.3(SNTA1):c.390T>C (p.Phe130=)	rs2146808171
NM_003098.3(SNTA1):c.414G>T (p.Val138=)
NM_003098.3(SNTA1):c.496+12C>T
NM_003098.3(SNTA1):c.496+13G>A
NM_003098.3(SNTA1):c.497-14TC[4]	rs752630265
NM_003098.3(SNTA1):c.582C>T (p.Pro194=)
NM_003098.3(SNTA1):c.649T>C (p.Leu217=)	rs1555818113
NM_003098.3(SNTA1):c.669G>A (p.Ser223=)	rs199762207
NM_003098.3(SNTA1):c.684C>T (p.Pro228=)
NM_003098.3(SNTA1):c.699C>T (p.Pro233=)
NM_003098.3(SNTA1):c.701+10G>C
NM_003098.3(SNTA1):c.702-13T>A
NM_003098.3(SNTA1):c.702-13T>C
NM_003098.3(SNTA1):c.702-7C>A	rs780688953
NM_003098.3(SNTA1):c.702-8G>A
NM_003098.3(SNTA1):c.750G>A (p.Arg250=)	rs1014697667
NM_003098.3(SNTA1):c.756G>A (p.Lys252=)
NM_003098.3(SNTA1):c.783G>A (p.Ala261=)
NM_003098.3(SNTA1):c.798C>T (p.Ala266=)
NM_003098.3(SNTA1):c.822G>A (p.Arg274=)
NM_003098.3(SNTA1):c.840G>A (p.Gln280=)
NM_003098.3(SNTA1):c.910-9del
NM_003098.3(SNTA1):c.939G>T (p.Leu313=)	rs1181358730
NM_003098.3(SNTA1):c.969C>T (p.Leu323=)
NM_003098.3(SNTA1):c.975G>A (p.Leu325=)
NM_003098.3(SNTA1):c.981C>T (p.Leu327=)
NM_003098.3(SNTA1):c.984C>G (p.Pro328=)	rs138863915

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