C0032027[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 402483	NM_001366385.1(CARD14):c.633G>A (p.Glu211=)	CARD14	Single nucleotide variant (synonymous variant +1 more)	Psoriasis 2 +3 more	GConflicting classifications of pathogenicity
Select item 1192693	NM_001366385.1(CARD14):c.675+26G>A	CARD14	Single nucleotide variant (intron variant)	Pityriasis rubra pilaris +3 more	GConflicting classifications of pathogenicity
Select item 402484	NM_001366385.1(CARD14):c.676-6G>A	CARD14	Single nucleotide variant (intron variant)	not specified +3 more	GBenign
Select item 402485	NM_001366385.1(CARD14):c.1641G>C (p.Arg547Ser)	CARD14 (R547S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GBenign
Select item 1192694	NM_001366385.1(CARD14):c.1852-60T>C	CARD14, SGSH	Single nucleotide variant (intron variant)	Pityriasis rubra pilaris +3 more	GBenign
Select item 1192695	NM_001366385.1(CARD14):c.1979-125C>A	CARD14, SGSH	Single nucleotide variant (intron variant)	Pityriasis rubra pilaris +2 more	GBenign
Select item 402482	NM_001366385.1(CARD14):c.2219+14T>A	CARD14, SGSH	Single nucleotide variant (3 prime UTR variant +1 more)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 1192536	NM_001366385.1(CARD14):c.2398+30A>G	CARD14, SGSH	Single nucleotide variant (intron variant)	Pityriasis rubra pilaris +3 more	GBenign
Select item 1192537	NM_001366385.1(CARD14):c.2398+42T>C	CARD14, SGSH	Single nucleotide variant (intron variant)	Pityriasis rubra pilaris +3 more	GBenign
Select item 1192538	NM_001366385.1(CARD14):c.2398+49G>A	CARD14, SGSH	Single nucleotide variant (intron variant)	Pityriasis rubra pilaris +3 more	GBenign
Select item 402486	NM_001366385.1(CARD14):c.2399-4A>G	LOC126862662, SGSH +1 more	Single nucleotide variant (intron variant)	not specified +3 more	GBenign; association
Select item 402487	NM_001366385.1(CARD14):c.2458C>T (p.Arg820Trp)	CARD14, LOC126862662 +1 more (R820W)	Single nucleotide variant (missense variant +1 more)	Psoriasis 2 +4 more	GConflicting classifications of pathogenicity