"PreventionGenetics, part of Exact Sciences"[submitter] AND "DENND4B"[ - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3034631	NM_014856.3(DENND4B):c.4419C>T (p.His1473=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related condition	GLikely benign
Select item 3051405	NM_014856.3(DENND4B):c.4374C>G (p.Ala1458=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related condition	GLikely benign
Select item 3044596	NM_014856.3(DENND4B):c.4311A>G (p.Thr1437=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related condition	GBenign
Select item 3033743	NM_014856.3(DENND4B):c.3913T>C (p.Leu1305=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related condition	GLikely benign
Select item 3048236	NM_014856.3(DENND4B):c.3624-6C>T	DENND4B	Single nucleotide variant (intron variant)	DENND4B-related condition	GLikely benign
Select item 3052285	NM_014856.3(DENND4B):c.3269G>A (p.Arg1090His)	DENND4B (R1090H +1 more)	Single nucleotide variant (missense variant)	DENND4B-related condition	GLikely benign
Select item 3048357	NM_014856.3(DENND4B):c.3036G>A (p.Pro1012=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related condition	GLikely benign
Select item 599506	NM_014856.3(DENND4B):c.2828G>C (p.Trp943Ser)	DENND4B (W943S +1 more)	Single nucleotide variant (missense variant)	DENND4B-related condition	GLikely benign
Select item 3061201	NM_014856.3(DENND4B):c.2704CAG[16] (p.Gln910_Glu911insGlnGlnGlnGlnGlnGlnGln)	DENND4B	Microsatellite (inframe insertion)	DENND4B-related condition	GUncertain significance
Select item 3042126	NM_014856.3(DENND4B):c.2704CAG[10] (p.Gln910_Glu911insGln)	DENND4B	Microsatellite (inframe insertion)	DENND4B-related condition	GLikely benign
Select item 3059203	NM_014856.3(DENND4B):c.2704CAG[6] (p.Gln908_Gln910del)	DENND4B	Microsatellite (inframe deletion)	DENND4B-related condition	GBenign
Select item 3033510	NM_014856.3(DENND4B):c.2703_2729del (p.Gln902_Gln910del)	DENND4B	Deletion (inframe deletion)	DENND4B-related condition	GLikely benign
Select item 3037524	NM_014856.3(DENND4B):c.2703A>G (p.Gln901=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related condition	GBenign
Select item 3043052	NM_014856.3(DENND4B):c.2439+10C>T	DENND4B	Single nucleotide variant (intron variant)	DENND4B-related condition	GLikely benign
Select item 3052690	NM_014856.3(DENND4B):c.2103C>T (p.Tyr701=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related condition	GBenign
Select item 3051109	NM_014856.3(DENND4B):c.1905G>A (p.Glu635=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related condition	GLikely benign
Select item 3058049	NM_014856.3(DENND4B):c.1819+4T>C	DENND4B	Single nucleotide variant (intron variant)	DENND4B-related condition	GLikely benign
Select item 3046379	NM_014856.3(DENND4B):c.1665G>A (p.Val555=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related condition	GLikely benign
Select item 2633376	NM_014856.3(DENND4B):c.1318C>G (p.Leu440Val)	DENND4B (L440V +1 more)	Single nucleotide variant (missense variant)	DENND4B-related condition	GUncertain significance
Select item 2639363	NM_014856.3(DENND4B):c.1317C>G (p.Ala439=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related condition +1 more	GLikely benign
Select item 3033812	NM_014856.3(DENND4B):c.1056-3del	DENND4B	Deletion (intron variant)	DENND4B-related condition	GLikely benign
Select item 3050560	NM_014856.3(DENND4B):c.948T>C (p.Arg316=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related condition	GLikely benign
Select item 3053889	NM_014856.3(DENND4B):c.897C>T (p.Ser299=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related condition	GLikely benign
Select item 3045601	NM_014856.3(DENND4B):c.843G>A (p.Ala281=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related condition	GBenign
Select item 3049934	NM_014856.3(DENND4B):c.703G>A (p.Val235Ile)	DENND4B (V235I +1 more)	Single nucleotide variant (missense variant)	DENND4B-related condition	GLikely benign
Select item 3057373	NM_014856.3(DENND4B):c.690C>T (p.Pro230=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related condition	GLikely benign
Select item 2371083	NM_014856.3(DENND4B):c.371C>T (p.Thr124Met)	DENND4B (T135M +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2591016	NM_014856.3(DENND4B):c.307G>A (p.Val103Ile)	DENND4B (V114I +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3044585	NM_014856.3(DENND4B):c.108G>C (p.Gly36=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related condition	GBenign
Select item 2628853	NM_014856.3(DENND4B):c.46G>A (p.Ala16Thr)	DENND4B (A16T +1 more)	Single nucleotide variant (missense variant)	DENND4B-related condition	GUncertain significance
Select item 3056982	NM_014856.3(DENND4B):c.39C>T (p.Phe13=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related condition	GLikely benign
Select item 2639364	NM_014856.3(DENND4B):c.30G>A (p.Val10=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related condition +1 more	GLikely benign
Select item 3055732	NM_014856.3(DENND4B):c.-6G>C	DENND4B (G10R)	Single nucleotide variant (missense variant +1 more)	DENND4B-related condition	GBenign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 33