"Ambry Genetics"[submitter] AND "HOXD8"[gene] - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2299094	NM_019558.4(HOXD8):c.31T>C (p.Ser11Pro)	HOXD8, LOC100129455 (S11P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249915	NM_019558.4(HOXD8):c.88A>C (p.Thr30Pro)	HOXD8, LOC100129455 (T30P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106751	NM_019558.4(HOXD8):c.118G>A (p.Val40Ile)	HOXD8, LOC100129455 (V40I)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2569321	NM_019558.4(HOXD8):c.127C>T (p.Arg43Cys)	HOXD8, LOC100129455 (R43C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393736	NM_019558.4(HOXD8):c.130C>T (p.His44Tyr)	HOXD8, LOC100129455 (H44Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2320582	NM_019558.4(HOXD8):c.130C>G (p.His44Asp)	HOXD8, LOC100129455 (H44D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2305757	NM_019558.4(HOXD8):c.139G>T (p.Ala47Ser)	HOXD8, LOC100129455 (A47S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2240763	NM_019558.4(HOXD8):c.143C>A (p.Ala48Glu)	HOXD8, LOC100129455 (A48E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267198	NM_019558.4(HOXD8):c.169A>C (p.Ser57Arg)	HOXD8 (S57R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106752	NM_019558.4(HOXD8):c.211C>T (p.His71Tyr)	HOXD8 (H71Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106753	NM_019558.4(HOXD8):c.212A>C (p.His71Pro)	HOXD8 (H71P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2220729	NM_019558.4(HOXD8):c.213C>A (p.His71Gln)	HOXD8 (H71Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3284703	NM_019558.4(HOXD8):c.220C>T (p.Pro74Ser)	HOXD8 (P74S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106754	NM_019558.4(HOXD8):c.221C>T (p.Pro74Leu)	HOXD8 (P74L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234509	NM_019558.4(HOXD8):c.224C>G (p.Ser75Cys)	HOXD8 (S75C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3284702	NM_019558.4(HOXD8):c.250G>A (p.Gly84Ser)	HOXD8 (G84S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244019	NM_019558.4(HOXD8):c.298A>C (p.Ser100Arg)	HOXD8 (S100R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3284701	NM_019558.4(HOXD8):c.311C>T (p.Ala104Val)	HOXD8 (A104V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2522234	NM_019558.4(HOXD8):c.325C>T (p.Pro109Ser)	HOXD8 (P109S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106755	NM_019558.4(HOXD8):c.328C>T (p.Pro110Ser)	HOXD8 (P110S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3284706	NM_019558.4(HOXD8):c.329C>A (p.Pro110His)	HOXD8 (P110H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546708	NM_019558.4(HOXD8):c.347C>A (p.Pro116Gln)	HOXD8 (P116Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542253	NM_019558.4(HOXD8):c.364C>A (p.Pro122Thr)	HOXD8 (P122T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106756	NM_019558.4(HOXD8):c.382G>A (p.Ala128Thr)	HOXD8 (A128T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3284704	NM_019558.4(HOXD8):c.404A>G (p.Lys135Arg)	HOXD8 (K135R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2291767	NM_019558.4(HOXD8):c.421A>C (p.Asn141His)	HOXD8 (N141H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2284147	NM_019558.4(HOXD8):c.455A>C (p.Gln152Pro)	HOXD8 (Q152P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106757	NM_019558.4(HOXD8):c.569G>A (p.Arg190Lys)	HOXD8 (R190K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231769	NM_019558.4(HOXD8):c.583C>T (p.Pro195Ser)	HOXD8 (P195S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363613	NM_019558.4(HOXD8):c.670A>G (p.Arg224Gly)	HOXD8 (R224G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494615	NM_019558.4(HOXD8):c.703G>A (p.Ala235Thr)	HOXD8 (A51T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3284705	NM_019558.4(HOXD8):c.742A>G (p.Arg248Gly)	HOXD8 (R247G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285559	NM_019558.4(HOXD8):c.835G>A (p.Glu279Lys)	HOXD8 (E95K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 33