PCID2[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3305121	NM_001127202.4(PCID2):c.1190C>T (p.Thr397Met)	PCID2 (T355M +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 732181	NM_001127202.4(PCID2):c.1111-4G>A	PCID2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2622317	NM_001127202.4(PCID2):c.883C>A (p.His295Asn)	PCID2 (H293N +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3210203	NM_001127202.4(PCID2):c.856G>A (p.Val286Met)	PCID2 (V119M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339350	NM_001127202.4(PCID2):c.748A>G (p.Met250Val)	PCID2 (M250V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557882	NM_001127202.4(PCID2):c.728C>G (p.Ser243Cys)	PCID2 (S241C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3305122	NM_001127202.4(PCID2):c.694T>G (p.Tyr232Asp)	PCID2 (Y190D +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394500	NM_001127202.4(PCID2):c.673G>A (p.Asp225Asn)	PCID2 (D183N +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 734849	NM_001127202.4(PCID2):c.405G>T (p.Gly135=)	PCID2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2312684	NM_001127202.4(PCID2):c.280G>A (p.Ala94Thr)	PCID2 (A94T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3210202	NM_001127202.4(PCID2):c.278G>A (p.Arg93Gln)	PCID2 (R147Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3210200	NM_001127202.4(PCID2):c.248G>A (p.Cys83Tyr)	PCID2 (C41Y +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2537239	NM_001127202.4(PCID2):c.43G>A (p.Glu15Lys)	PCID2 (E13K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance