Related gene-specific medical variations for Gene (Select 8805) - ClinVar - NCBI

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Links from Gene

Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3182304	NM_015905.3(TRIM24):c.352T>G (p.Phe118Val)	LOC129999452, TRIM24 (F118V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534701	NM_015905.3(TRIM24):c.296C>G (p.Ala99Gly)	LOC129999452, TRIM24 (A99G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534700	NM_015905.3(TRIM24):c.133G>A (p.Gly45Ser)	LOC129999452, TRIM24 (G45S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2445371	NM_015905.3(TRIM24):c.2338T>A (p.Ser780Thr)	TRIM24 (S746T +1 more)	Single nucleotide variant (missense variant)	Ovarian cancer	GBenign
Select item 2445349	NM_015905.3(TRIM24):c.2050C>T (p.Arg684Cys)	TRIM24 (R650C +1 more)	Single nucleotide variant (missense variant)	Ovarian cancer	GLikely pathogenic
Select item 2445296	NM_015905.3(TRIM24):c.259C>T (p.Arg87Cys)	TRIM24, LOC129999452 (R87C)	Single nucleotide variant (missense variant)	Ovarian cancer	GBenign
Select item 2445247	NM_015905.3(TRIM24):c.2899G>A (p.Ala967Thr)	TRIM24 (A933T +1 more)	Single nucleotide variant (missense variant)	Ovarian cancer	GBenign
Select item 2445236	NM_015905.3(TRIM24):c.76G>A (p.Ala26Thr)	TRIM24 (A26T)	Single nucleotide variant (missense variant)	Ovarian cancer	GBenign
Select item 2401832	NM_015905.3(TRIM24):c.341G>T (p.Gly114Val)	LOC129999452, TRIM24 (G114V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384345	NM_015905.3(TRIM24):c.55G>C (p.Ala19Pro)	LOC129999451, TRIM24 (A19P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382082	NM_015905.3(TRIM24):c.290G>C (p.Gly97Ala)	LOC129999452, TRIM24 (G97A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360429	NM_015905.3(TRIM24):c.44C>T (p.Ala15Val)	LOC129999451, TRIM24 (A15V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326628	NM_015905.3(TRIM24):c.257A>T (p.Gln86Leu)	LOC129999452, TRIM24 (Q86L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214716	NM_015905.3(TRIM24):c.193A>T (p.Ser65Cys)	LOC129999452, TRIM24 (S65C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance