"PreventionGenetics, part of Exact Sciences"[submitter] AND "SNTA1"[ge - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 496193	NM_003098.3(SNTA1):c.*8C>T	SNTA1	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 215503	NM_003098.3(SNTA1):c.1426-5T>C	SNTA1	Single nucleotide variant (intron variant)	Long QT syndrome +4 more	GBenign/Likely benign
Select item 191548	NM_003098.3(SNTA1):c.770C>G (p.Ala257Gly)	SNTA1 (A257G)	Single nucleotide variant (missense variant)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 190911	NM_003098.3(SNTA1):c.677G>A (p.Cys226Tyr)	SNTA1 (C226Y)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +4 more	GConflicting classifications of pathogenicity
Select item 1741549	NM_003098.3(SNTA1):c.456G>A (p.Val152=)	SNTA1	Single nucleotide variant (synonymous variant)	SNTA1-related disorder +1 more	GLikely benign
Select item 511314	NM_003098.3(SNTA1):c.339C>G (p.Leu113=)	SNTA1	Single nucleotide variant (synonymous variant)	SNTA1-related disorder +3 more	GLikely benign
Select item 36777	NM_003098.3(SNTA1):c.311-6G>C	SNTA1	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 1147833	NM_003098.3(SNTA1):c.279C>A (p.Ala93=)	LOC130065679, SNTA1	Single nucleotide variant (synonymous variant)	SNTA1-related disorder +2 more	GLikely benign
Select item 1543594	NM_003098.3(SNTA1):c.240G>T (p.Ala80=)	SNTA1	Single nucleotide variant (synonymous variant)	SNTA1-related disorder +1 more	GLikely benign
Select item 258904	NM_003098.3(SNTA1):c.229C>T (p.Leu77=)	SNTA1	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 263476	NM_003098.3(SNTA1):c.221C>T (p.Pro74Leu)	SNTA1 (P74L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +5 more	GConflicting classifications of pathogenicity
Select item 2629505	NM_003098.3(SNTA1):c.62C>T (p.Ser21Leu)	LOC130065680, SNTA1 (S21L)	Single nucleotide variant (missense variant)	SNTA1-related disorder +1 more	GConflicting classifications of pathogenicity