Related gene-specific medical variations for Gene (Select 23650) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3328690	NM_012101.4(TRIM29):c.1243G>A (p.Asp415Asn)	LOC112042780, TRIM29 (D415N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458198	NM_012101.4(TRIM29):c.1264C>T (p.Arg422Cys)	LOC112042780, TRIM29 (R161C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400747	NM_012101.4(TRIM29):c.1229G>A (p.Gly410Asp)	LOC112042780, TRIM29 (G149D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362959	NM_012101.4(TRIM29):c.1300C>T (p.Arg434Cys)	LOC112042780, TRIM29 (R173C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353737	NM_012101.4(TRIM29):c.1289C>T (p.Ala430Val)	LOC112042780, TRIM29 (A169V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294321	NM_012101.4(TRIM29):c.1281G>A (p.Met427Ile)	LOC112042780, TRIM29 (M166I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279889	NM_012101.4(TRIM29):c.1301G>C (p.Arg434Pro)	LOC112042780, TRIM29 (R173P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246577	NM_012101.4(TRIM29):c.1270G>A (p.Val424Ile)	LOC112042780, TRIM29 (V424I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 781049	NM_012101.4(TRIM29):c.1333+8C>A	LOC112042780, TRIM29	Single nucleotide variant (intron variant)	not provided	GBenign