Related gene-specific medical variations for Gene (Select 573) - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3260006	NM_004323.6(BAG1):c.47G>T (p.Arg16Leu)	BAG1, LOC130001652 (R16L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3259995	NM_004323.6(BAG1):c.209C>G (p.Pro70Arg)	BAG1, LOC130001651 (P70R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3132799	NM_004323.6(BAG1):c.411G>T (p.Glu137Asp)	BAG1, LOC130001651 (E22D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3132798	NM_004323.6(BAG1):c.391A>G (p.Ser131Gly)	BAG1, LOC130001651 (S16G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3132797	NM_004323.6(BAG1):c.346A>G (p.Met116Val)	BAG1, LOC130001651 (M116V +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3132796	NM_004323.6(BAG1):c.190G>A (p.Ala64Thr)	BAG1, LOC130001651 (A64T)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2530726	NM_004323.6(BAG1):c.194C>T (p.Ala65Val)	BAG1, LOC130001651 (A65V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2470058	NM_004323.6(BAG1):c.146C>T (p.Ala49Val)	BAG1, LOC130001652 (A49V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2465033	NM_004323.6(BAG1):c.131C>T (p.Ser44Phe)	BAG1, LOC130001652 (S44F)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2404474	NM_004323.6(BAG1):c.244C>T (p.Arg82Trp)	BAG1, LOC130001651 (R11W +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2393791	NM_004323.6(BAG1):c.73C>T (p.Arg25Trp)	BAG1, LOC130001652 (R25W)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2356886	NM_004323.6(BAG1):c.46C>T (p.Arg16Trp)	BAG1, LOC130001652 (R16W)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2292146	NM_004323.6(BAG1):c.14G>T (p.Gly5Val)	BAG1, LOC130001652 (G5V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2276052	NM_004323.6(BAG1):c.146C>G (p.Ala49Gly)	BAG1, LOC130001652 (A49G)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2257643	NM_004323.6(BAG1):c.328G>A (p.Ala110Thr)	BAG1, LOC130001651 (A39T +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2238478	NM_004323.6(BAG1):c.134G>T (p.Gly45Val)	BAG1, LOC130001652 (G45V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance