Related gene-specific medical variations for Gene (Select 639) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3309738	NM_001198.4(PRDM1):c.425G>A (p.Gly142Glu)	LOC126859755, PRDM1 (G142E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 135091	NM_001198.4(PRDM1):c.2312G>A (p.Gly771Asp)	PRDM1 (G771D +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135090	NM_001198.4(PRDM1):c.2233G>A (p.Val745Met)	PRDM1 (V745M +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135088	NM_001198.4(PRDM1):c.1141T>C (p.Tyr381His)	PRDM1 (Y381H +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135087	NM_001198.4(PRDM1):c.1222G>C (p.Ala408Pro)	PRDM1 (A408P +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135086	NM_001198.4(PRDM1):c.1061G>A (p.Ser354Asn)	PRDM1 (S354N +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135084	NM_001198.4(PRDM1):c.1400C>T (p.Pro467Leu)	PRDM1 (P467L +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135082	NM_001198.4(PRDM1):c.1148C>T (p.Thr383Met)	PRDM1 (T383M +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135081	NM_001198.4(PRDM1):c.1100C>T (p.Ser367Phe)	PRDM1 (S367F +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135080	NM_001198.4(PRDM1):c.1306A>G (p.Asn436Asp)	PRDM1 (N436D +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135079	NM_001198.4(PRDM1):c.1147A>G (p.Thr383Ala)	PRDM1 (T383A +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135077	NM_001198.4(PRDM1):c.448G>A (p.Gly150Ser)	LOC126859755, PRDM1 (G150S +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135075	NM_001198.4(PRDM1):c.502C>G (p.Pro168Ala)	PRDM1 (P168A +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135074	NM_001198.4(PRDM1):c.220G>A (p.Gly74Ser)	PRDM1 (G74S)	Single nucleotide variant (missense variant)	not specified	Gnot provided