Related gene-specific medical variations for Gene (Select 83648) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3091968	NM_053279.3(FAM167A):c.619A>G (p.Asn207Asp)	FAM167A, FAM167A-AS1 (N207D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091967	NM_053279.3(FAM167A):c.545G>T (p.Cys182Phe)	FAM167A, FAM167A-AS1 (C182F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091966	NM_053279.3(FAM167A):c.427C>T (p.Arg143Cys)	FAM167A, FAM167A-AS1 (R143C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2658403	NM_053279.3(FAM167A):c.600C>T (p.Gly200=)	FAM167A, FAM167A-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2534043	NM_053279.3(FAM167A):c.580A>G (p.Thr194Ala)	FAM167A, FAM167A-AS1 (T194A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389209	NM_053279.3(FAM167A):c.485G>T (p.Arg162Met)	FAM167A, FAM167A-AS1 (R162M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338641	NM_053279.3(FAM167A):c.528G>C (p.Glu176Asp)	FAM167A, FAM167A-AS1 (E176D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329463	NM_053279.3(FAM167A):c.439G>A (p.Asp147Asn)	FAM167A, FAM167A-AS1 (D147N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270377	NM_053279.3(FAM167A):c.635C>A (p.Ser212Tyr)	FAM167A, FAM167A-AS1 (S212Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance