"PreventionGenetics, part of Exact Sciences"[submitter] AND "SRA1"[gen - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 785142	NM_001035235.4(SRA1):c.653C>T (p.Pro218Leu)	SRA1 (P202L +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 1301591	NM_001035235.4(SRA1):c.500T>C (p.Ile167Thr)	SRA1 (I151T +1 more)	Single nucleotide variant (missense variant +1 more)	SRA1-related disorder +2 more	GBenign/Likely benign
Select item 1591816	NM_001035235.4(SRA1):c.413G>A (p.Gly138Glu)	SRA1 (G122E +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 3040039	NM_001035235.4(SRA1):c.314C>T (p.Pro105Leu)	SRA1 (P105L)	Single nucleotide variant (missense variant +2 more)	SRA1-related disorder	GLikely benign
Select item 1549469	NM_001035235.4(SRA1):c.230C>T (p.Pro77Leu)	SRA1 (P77L)	Single nucleotide variant (missense variant +2 more)	SRA1-related disorder +1 more	GLikely benign
Select item 1608102	NM_001035235.4(SRA1):c.182C>T (p.Pro61Leu)	SRA1 (P61L)	Single nucleotide variant (missense variant +2 more)	SRA1-related disorder +1 more	GBenign/Likely benign
Select item 1335598	NM_001035235.4(SRA1):c.58C>G (p.Gln20Glu)	SRA1 (Q20E)	Single nucleotide variant (missense variant +2 more)	SRA1-related disorder +1 more	GBenign/Likely benign
Select item 785143	NM_001035235.4(SRA1):c.48C>T (p.Asn16=)	SRA1 (T68M)	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GBenign
Select item 3058167	NM_001035235.4(SRA1):c.26-11C>T	SRA1 (S57L)	Single nucleotide variant (missense variant +2 more)	SRA1-related disorder	GLikely benign
Select item 3041584	NM_001035235.4(SRA1):c.26-64C>T	SRA1	Single nucleotide variant (synonymous variant +2 more)	SRA1-related disorder	GLikely benign
Select item 3044899	NM_001035235.3(SRA1):c.-6C>G	SRA1	Single nucleotide variant (non-coding transcript variant)	SRA1-related disorder	GLikely benign