"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "DCPS"[gene - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2642531	NM_014026.6(DCPS):c.240C>T (p.Ala80=)	DCPS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642532	NM_014026.6(DCPS):c.377-1024C>T	DCPS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2642533	NM_014026.6(DCPS):c.510C>T (p.Ser170=)	DCPS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 712729	NM_014026.6(DCPS):c.558G>A (p.Ala186=)	DCPS	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1176928	NM_014026.6(DCPS):c.637-6A>G	DCPS, GSEC	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1879218	NM_014026.6(DCPS):c.670C>T (p.Arg224Cys)	GSEC, DCPS (R224C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 376909	NM_014026.6(DCPS):c.677G>A (p.Gly226Asp)	DCPS, GSEC (G226D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GBenign/Likely benign
Select item 749774	NM_014026.6(DCPS):c.804C>T (p.His268=)	DCPS, GSEC	Single nucleotide variant (synonymous variant)	DCPS-related condition +1 more	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 2642534	NM_014026.6(DCPS):c.861C>T (p.Ala287=)	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)	DCPS-related condition +1 more	GLikely benign
Select item 3026246	NM_014026.6(DCPS):c.897T>C (p.Ala299=)	DCPS, GSEC	Single nucleotide variant (synonymous 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 775095	NM_014026.6(DCPS):c.1013G>A (p.Ter338=)	DCPS, GSEC	Single nucleotide variant (synonymous variant)	DCPS-related condition +1 more	GBenign/Likely benign