Related gene-specific medical variations for Gene (Select 84925) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3165011	NM_032839.3(SLC49A4):c.76T>A (p.Ser26Thr)	LOC129937389, SLC49A4 (S26T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165009	NM_032839.3(SLC49A4):c.62C>G (p.Pro21Arg)	LOC129937389, SLC49A4 (P21R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165004	NM_032839.3(SLC49A4):c.133G>T (p.Gly45Trp)	LOC129937389, SLC49A4 (G45W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594825	NM_032839.3(SLC49A4):c.58G>C (p.Gly20Arg)	LOC129937389, SLC49A4 (G20R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536873	NM_032839.3(SLC49A4):c.94G>A (p.Ala32Thr)	LOC129937389, SLC49A4 (A32T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484021	NM_032839.3(SLC49A4):c.107C>T (p.Ala36Val)	LOC129937389, SLC49A4 (A36V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2445280	NM_032839.3(SLC49A4):c.1133C>A (p.Thr378Asn)	SLC49A4 (T378N)	Single nucleotide variant (missense variant)	Ovarian cancer	GBenign
Select item 2445277	NM_032839.3(SLC49A4):c.112C>T (p.Pro38Ser)	LOC129937389, SLC49A4 (P38S)	Single nucleotide variant (missense variant)	Ovarian cancer	GBenign

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