"PreventionGenetics, part of Exact Sciences"[submitter] AND "CASP10"[g - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2632986	NM_032977.4(CASP10):c.131T>C (p.Ile44Thr)	CASP10 (I44T)	Single nucleotide variant (missense variant)	CASP10-related disorder	GUncertain significance
Select item 333417	NM_032977.4(CASP10):c.174C>T (p.Ala58=)	CASP10	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 2632930	NM_032977.4(CASP10):c.466C>G (p.Leu156Val)	CASP10 (L156V)	Single nucleotide variant (missense variant)	CASP10-related disorder	GUncertain significance
Select item 565644	NM_032977.4(CASP10):c.507C>G (p.Cys169Trp)	CASP10 (C169W)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A +1 more	GUncertain significance
Select item 3048244	NM_032977.4(CASP10):c.606C>T (p.Asp202=)	CASP10	Single nucleotide variant (synonymous variant)	CASP10-related disorder	GLikely benign
Select item 2634914	NM_032977.4(CASP10):c.623A>G (p.Tyr208Cys)	CASP10 (Y208C)	Single nucleotide variant (missense variant)	CASP10-related disorder	GUncertain significance
Select item 661386	NM_032977.4(CASP10):c.664A>G (p.Thr222Ala)	CASP10 (T222A)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A +2 more	GUncertain significance
Select item 1916910	NM_032977.4(CASP10):c.684+4G>T	CASP10	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 2A +1 more	GConflicting classifications of pathogenicity
Select item 467717	NM_032977.4(CASP10):c.715A>T (p.Ser239Cys)	CASP10 (S239C)	Single nucleotide variant (missense variant +1 more)	CASP10-related disorder +1 more	GLikely benign
Select item 961874	NM_032977.4(CASP10):c.838C>T (p.Arg280Trp)	CASP10 (S249L +2 more)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 2A +1 more	GUncertain significance
Select item 753583	NM_032977.4(CASP10):c.1041C>T (p.Asp347=)	CASP10	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 2A +1 more	GLikely benign
Select item 3029247	NM_032977.4(CASP10):c.1044G>A (p.Gly348=)	CASP10	Single nucleotide variant (synonymous variant +1 more)	CASP10-related disorder	GLikely benign
Select item 1251933	NM_032977.4(CASP10):c.1159C>G (p.Pro387Ala)	CASP10 (P320A +2 more)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 2A +2 more	GUncertain significance
Select item 2058509	NM_032977.4(CASP10):c.1198G>A (p.Ala400Thr)	CASP10 (A357T +2 more)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 2A +1 more	GUncertain significance
Select item 535760	NM_032977.4(CASP10):c.1202_1208del (p.Cys401fs)	CASP10 (C334fs +2 more)	Deletion (frameshift variant +1 more)	CASP10-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 333439	NM_032977.4(CASP10):c.1415+8C>G	CASP10	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 2A +1 more	GBenign/Likely benign
Select item 743264	NM_032977.4(CASP10):c.1452C>T (p.Asn484=)	CASP10	Single nucleotide variant (synonymous variant +2 more)	CASP10-related disorder +1 more	GLikely benign
Select item 2635032	NM_001206542.2(CASP10):c.1414C>G (p.Arg472Gly)	CASP10 (R472G +1 more)	Single nucleotide variant (missense variant)	CASP10-related disorder	GUncertain significance