"Ambry Genetics"[submitter] AND "DENND10"[gene] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3081418	NM_207009.4(DENND10):c.8C>T (p.Ala3Val)	DENND10, LOC130004824 (A3V)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3081406	NM_207009.4(DENND10):c.44T>C (p.Val15Ala)	DENND10, LOC130004824 (V15A)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2481861	NM_207009.4(DENND10):c.47G>C (p.Gly16Ala)	DENND10, LOC130004824 (G16A)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2485295	NM_207009.4(DENND10):c.104C>T (p.Thr35Met)	DENND10 (T35M +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3081405	NM_207009.4(DENND10):c.247A>C (p.Lys83Gln)	DENND10 (K83Q +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2551596	NM_207009.4(DENND10):c.380T>C (p.Ile127Thr)	DENND10 (I54T +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3081407	NM_207009.4(DENND10):c.452G>A (p.Arg151Gln)	DENND10 (R151Q +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3081408	NM_207009.4(DENND10):c.479A>G (p.Lys160Arg)	DENND10 (K160R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2495048	NM_207009.4(DENND10):c.500G>A (p.Gly167Glu)	DENND10 (G159E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081410	NM_207009.4(DENND10):c.553G>A (p.Val185Met)	DENND10 (V112M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530203	NM_207009.4(DENND10):c.590C>T (p.Thr197Ile)	DENND10 (T124I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081411	NM_207009.4(DENND10):c.608T>C (p.Leu203Pro)	DENND10 (L130P +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2616360	NM_207009.4(DENND10):c.632C>T (p.Thr211Ile)	DENND10 (T138I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3081412	NM_207009.4(DENND10):c.652C>T (p.His218Tyr)	DENND10 (H67Y +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3081413	NM_207009.4(DENND10):c.661G>A (p.Ala221Thr)	DENND10 (A213T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3081414	NM_207009.4(DENND10):c.761A>G (p.Asn254Ser)	DENND10 (N103S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3081415	NM_207009.4(DENND10):c.785T>C (p.Ile262Thr)	DENND10 (I111T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3081416	NM_207009.4(DENND10):c.823C>G (p.Leu275Val)	DENND10 (L202V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532727	NM_207009.4(DENND10):c.886C>T (p.His296Tyr)	DENND10 (H296Y +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3081417	NM_207009.4(DENND10):c.896A>G (p.Gln299Arg)	DENND10 (Q299R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 20