Related gene-specific medical variations for Gene (Select 79961) - ClinVar - NCBI

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Links from Gene

Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3271551	NM_024901.5(DENND2D):c.1244C>T (p.Ser415Phe)	DENND2D, LOC126805826 (S412F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271549	NM_024901.5(DENND2D):c.1177T>C (p.Tyr393His)	DENND2D, LOC126805826 (Y390H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271546	NM_024901.5(DENND2D):c.1186C>T (p.Arg396Trp)	DENND2D, LOC126805826 (R393W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271544	NM_024901.5(DENND2D):c.22C>T (p.Arg8Trp)	DENND2D, LOC129931164 (R8W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3271543	NM_024901.5(DENND2D):c.44G>A (p.Arg15His)	DENND2D, LOC129931164 (R15H)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3081568	NM_024901.5(DENND2D):c.29T>G (p.Phe10Cys)	DENND2D, LOC129931164 (F10C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3081564	NM_024901.5(DENND2D):c.1322G>C (p.Ser441Thr)	DENND2D, LOC126805826 (S438T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081563	NM_024901.5(DENND2D):c.1193C>A (p.Ala398Glu)	DENND2D, LOC126805826 (A398E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615020	NM_024901.5(DENND2D):c.32G>A (p.Arg11Lys)	DENND2D, LOC129931164 (R11K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2594384	NM_024901.5(DENND2D):c.1220G>T (p.Arg407Ile)	DENND2D, LOC126805826 (R404I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589245	NM_024901.5(DENND2D):c.1117G>A (p.Glu373Lys)	DENND2D, LOC126805826 (E370K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263127	NM_024901.5(DENND2D):c.1219A>G (p.Arg407Gly)	DENND2D, LOC126805826 (R407G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215223	NM_024901.5(DENND2D):c.1172C>T (p.Ala391Val)	DENND2D, LOC126805826 (A391V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance