Related gene-specific medical variations for Gene (Select 9274) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3260665	NM_004765.4(BCL7C):c.643C>T (p.Pro215Ser)	BCL7C, MIR762HG (P215S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3133442	NM_004765.4(BCL7C):c.220C>T (p.Arg74Cys)	BCL7C, MIR762HG (R74C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570243	NM_004765.4(BCL7C):c.422C>A (p.Pro141Gln)	BCL7C, MIR762HG (P141Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569200	NM_004765.4(BCL7C):c.535G>A (p.Glu179Lys)	BCL7C, MIR762HG (E179K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543387	NM_004765.4(BCL7C):c.251G>C (p.Gly84Ala)	BCL7C, MIR762HG (G84A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535517	NM_004765.4(BCL7C):c.109A>G (p.Thr37Ala)	BCL7C, MIR762HG (T37A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522976	NM_004765.4(BCL7C):c.602C>T (p.Ser201Leu)	BCL7C, MIR762HG (S201L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2332521	NM_004765.4(BCL7C):c.73A>G (p.Ile25Val)	BCL7C, MIR762HG (I25V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308011	NM_004765.4(BCL7C):c.188G>A (p.Gly63Asp)	BCL7C, MIR762HG (G63D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258897	NM_004765.4(BCL7C):c.224G>A (p.Arg75Gln)	BCL7C, MIR762HG (R75Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254400	NM_004765.4(BCL7C):c.308C>T (p.Ser103Leu)	BCL7C, MIR762HG (S103L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223266	NM_004765.4(BCL7C):c.425G>A (p.Arg142Gln)	BCL7C, MIR762HG (R142Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2205794	NM_004765.4(BCL7C):c.617C>A (p.Pro206Gln)	BCL7C, MIR762HG (P206Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1878504	NM_004765.4(BCL7C):c.528+3G>C	BCL7C, MIR762HG	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	Gnot provided