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

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_003098.3(SNTA1):c.496+111G>A	rs180921012	0.01416
NM_003098.3(SNTA1):c.1040+175G>A	rs77700180	0.00802
NM_003098.3(SNTA1):c.496+81G>T	rs150532233	0.00581
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.1488C>A (p.Ala496=)	rs34901081	0.00106
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.1080C>T (p.Tyr360=)	rs141844806	0.00019
NM_003098.3(SNTA1):c.1032C>T (p.Ile344=)	rs541665582	0.00015
NM_003098.3(SNTA1):c.311-20C>T	rs200764326	0.00013
NM_003098.3(SNTA1):c.847T>C (p.Leu283=)	rs754862058	0.00004
NM_003098.3(SNTA1):c.1437G>A (p.Leu479=)	rs780011608	0.00003
NM_003098.3(SNTA1):c.1440C>T (p.His480=)	rs201485963	0.00002
NM_003098.3(SNTA1):c.972C>T (p.Tyr324=)	rs761467167	0.00002
NM_003098.3(SNTA1):c.1011A>G (p.Pro337=)	rs758676160	0.00001
NM_003098.3(SNTA1):c.1386T>C (p.Ser462=)	rs1335638175	0.00001
NM_003098.3(SNTA1):c.173A>G (p.Glu58Gly)	rs555231776	0.00001
NM_003098.3(SNTA1):c.201C>T (p.Ala67=)	rs1403481465	0.00001
NM_003098.2(SNTA1):c.-382C>A	rs186369578
NM_003098.3(SNTA1):c.1517_*2dup (p.Ter506=)
NM_003098.3(SNTA1):c.162C>A (p.Gly54=)	rs544127915
NM_003098.3(SNTA1):c.207G>T (p.Glu69Asp)	rs2146814802
NM_003098.3(SNTA1):c.210G>T (p.Pro70=)	rs751651742
NM_003098.3(SNTA1):c.312C>T (p.Gly104=)	rs533476140
NM_003098.3(SNTA1):c.540T>C (p.Thr180=)	rs1600844808
NM_003098.3(SNTA1):c.552G>A (p.Ser184=)	rs781530478
NM_003098.3(SNTA1):c.771G>A (p.Ala257=)	rs113412654

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