List of variants in gene SNTA1 reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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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.828G>A (p.Lys276=)	rs35938843	0.00969
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.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.787G>T (p.Ala263Ser)	rs150576530	0.00054
NM_003098.3(SNTA1):c.1255C>T (p.Arg419Cys)	rs375515058	0.00001
NM_003098.3(SNTA1):c.205G>A (p.Glu69Lys)	rs1555822126
NM_003098.3(SNTA1):c.669G>A (p.Ser223=)	rs199762207

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