"Ambry Genetics"[submitter] AND "DTX4"[gene] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2323868	NM_015177.2(DTX4):c.43G>A (p.Glu15Lys)	DTX4, LOC121392917 (E15K)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2390005	NM_015177.2(DTX4):c.68G>A (p.Ser23Asn)	DTX4 (S23N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2622965	NM_015177.2(DTX4):c.208A>T (p.Thr70Ser)	DTX4 (T70S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2232171	NM_015177.2(DTX4):c.238T>C (p.Tyr80His)	DTX4 (Y80H)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2537086	NM_015177.2(DTX4):c.295A>C (p.Asn99His)	DTX4 (N99H)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2328762	NM_015177.2(DTX4):c.302C>G (p.Ser101Cys)	DTX4 (S101C)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2276245	NM_015177.2(DTX4):c.454C>T (p.Arg152Cys)	DTX4 (R46C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2595378	NM_015177.2(DTX4):c.463C>T (p.Arg155Trp)	DTX4 (R155W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2207270	NM_015177.2(DTX4):c.464G>A (p.Arg155Gln)	DTX4 (R155Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2528837	NM_015177.2(DTX4):c.511G>A (p.Ala171Thr)	DTX4 (A171T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2548694	NM_015177.2(DTX4):c.580T>C (p.Cys194Arg)	DTX4 (C194R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2395470	NM_015177.2(DTX4):c.594G>A (p.Met198Ile)	DTX4 (M198I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2477970	NM_015177.2(DTX4):c.697C>T (p.Pro233Ser)	DTX4 (P233S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2250867	NM_015177.2(DTX4):c.862G>C (p.Ala288Pro)	DTX4 (A182P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2543002	NM_015177.2(DTX4):c.887A>C (p.Asn296Thr)	DTX4 (N296T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2486923	NM_015177.2(DTX4):c.1057A>C (p.Lys353Gln)	DTX4 (K247Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2615678	NM_015177.2(DTX4):c.1174G>C (p.Glu392Gln)	DTX4 (E392Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2372235	NM_015177.2(DTX4):c.1573G>A (p.Ala525Thr)	DTX4 (A525T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2288268	NM_015177.2(DTX4):c.1657C>T (p.Arg553Cys)	DTX4 (R553C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2240146	NM_015177.2(DTX4):c.1699G>A (p.Glu567Lys)	DTX4 (E567K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2602719	NM_015177.2(DTX4):c.1838G>A (p.Ser613Asn)	DTX4 (S507N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 21