"PreventionGenetics, part of Exact Sciences"[submitter] AND "SERPINA3" - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3039814	NM_001085.5(SERPINA3):c.-6T>C	SERPINA3	Single nucleotide variant (5 prime UTR variant)	SERPINA3-related condition	GLikely benign
Select item 18051	NM_001085.5(SERPINA3):c.25G>A (p.Ala9Thr)	SERPINA3 (A9T)	Single nucleotide variant (missense variant)	SERPINA3-related condition +1 more	GBenign
Select item 2644481	NM_001085.5(SERPINA3):c.73C>T (p.Pro25Ser)	SERPINA3 (P25S)	Single nucleotide variant (missense variant)	SERPINA3-related condition +1 more	GLikely benign
Select item 3039878	NM_001085.5(SERPINA3):c.141C>T (p.Leu47=)	SERPINA3	Single nucleotide variant (synonymous variant)	SERPINA3-related condition	GLikely benign
Select item 403428	NM_001085.5(SERPINA3):c.303A>G (p.Lys101=)	SERPINA3	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 3041574	NM_001085.5(SERPINA3):c.363C>T (p.His121=)	SERPINA3	Single nucleotide variant (synonymous variant)	SERPINA3-related condition	GLikely benign
Select item 776856	NM_001085.5(SERPINA3):c.603G>A (p.Ser201=)	SERPINA3	Single nucleotide variant (synonymous variant)	SERPINA3-related condition +1 more	GBenign
Select item 708583	NM_001085.5(SERPINA3):c.710A>G (p.Lys237Arg)	SERPINA3 (K237R)	Single nucleotide variant (missense variant)	SERPINA3-related condition +1 more	GLikely benign
Select item 18050	NM_001085.5(SERPINA3):c.754C>G (p.Pro252Ala)	SERPINA3 (P252A)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2644484	NM_001085.5(SERPINA3):c.786C>A (p.Thr262=)	SERPINA3	Single nucleotide variant (synonymous variant)	SERPINA3-related condition +1 more	GLikely benign
Select item 3037686	NM_001085.5(SERPINA3):c.819C>T (p.Ser273=)	SERPINA3	Single nucleotide variant (synonymous variant)	SERPINA3-related condition	GBenign
Select item 728783	NM_001085.5(SERPINA3):c.893G>A (p.Arg298Gln)	SERPINA3 (R298Q)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3040753	NM_001085.5(SERPINA3):c.957G>A (p.Ser319=)	SERPINA3	Single nucleotide variant (synonymous variant)	SERPINA3-related condition	GLikely benign
Select item 3037310	NM_001085.5(SERPINA3):c.1041A>G (p.Thr347=)	SERPINA3	Single nucleotide variant (synonymous variant)	SERPINA3-related condition	GBenign