"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "GSEC"[g - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 376909	NM_014026.6(DCPS):c.677G>A (p.Gly226Asp)	GSEC, DCPS (G226D +1 more)	Single nucleotide variant (missense variant)	Al-Raqad syndrome +2 more	GBenign/Likely benign
Select item 732989	NM_014026.6(DCPS):c.717G>A (p.Pro239=)	DCPS, GSEC	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 377334	NM_014026.6(DCPS):c.791G>A (p.Arg264Gln)	DCPS, GSEC (R264Q +1 more)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 749774	NM_014026.6(DCPS):c.804C>T (p.His268=)	DCPS, GSEC	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 733947	NM_014026.6(DCPS):c.855C>T (p.Phe285=)	DCPS, GSEC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 782778	NM_014026.6(DCPS):c.868T>G (p.Ser290Ala)	DCPS, GSEC (S290A +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 733666	NM_014026.6(DCPS):c.906C>T (p.Ile302=)	DCPS, GSEC	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 733915	NM_014026.6(DCPS):c.954C>T (p.Thr318=)	DCPS, GSEC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 795094	NM_014026.6(DCPS):c.972C>T (p.Asp324=)	DCPS, GSEC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 718596	NM_014026.6(DCPS):c.977C>G (p.Pro326Arg)	DCPS, GSEC (P333R +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 775095	NM_014026.6(DCPS):c.1013G>A (p.Ter338=)	DCPS, GSEC	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign