"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "HOXD10"[ge - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2651560	NM_002148.4(HOXD10):c.211G>A (p.Val71Met)	HOXD10 (V71M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 332479	NM_002148.4(HOXD10):c.266G>A (p.Arg89Gln)	HOXD10 (R89Q)	Single nucleotide variant (missense variant)	Congenital vertical talus +1 more	GConflicting classifications of pathogenicity
Select item 425236	NM_002148.4(HOXD10):c.284C>A (p.Thr95Lys)	HOXD10 (T95K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 808888	NM_002148.4(HOXD10):c.292G>A (p.Val98Ile)	HOXD10 (V98I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 332480	NM_002148.4(HOXD10):c.372T>G (p.Ile124Met)	HOXD10 (I124M)	Single nucleotide variant (missense variant)	Congenital vertical talus +2 more	GConflicting classifications of pathogenicity
Select item 332484	NM_002148.4(HOXD10):c.561G>A (p.Lys187=)	HOXD10	Single nucleotide variant (synonymous variant)	Congenital vertical talus +1 more	GConflicting classifications of pathogenicity
Select item 3025750	NM_002148.4(HOXD10):c.619G>T (p.Gly207Cys)	HOXD10 (G207C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2651561	NM_002148.4(HOXD10):c.745+8T>G	HOXD10	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 332490	NM_002148.4(HOXD10):c.*2T>C	HOXD10	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 2651563	NM_002148.4(HOXD10):c.207_208insGTATATATATATATATATAT	HOXD10	Insertion (3 prime UTR variant)	not provided	GBenign
Select item 2651562	NM_002148.4(HOXD10):c.205_211TA[3]TGTATATATATATATATATATATAT[1]	HOXD10	Microsatellite (3 prime UTR variant)	not provided	GBenign
Select item 2651564	NM_002148.4(HOXD10):c.*234AT[6]AAA[1]	HOXD10	Microsatellite (3 prime UTR variant)	not provided	GBenign
Select item 2571102	NM_002148.4(HOXD10):c.*234AT[7]AAA[1]	HOXD10	Microsatellite (3 prime UTR variant)	not provided	GLikely benign
Select item 1694983	NM_002148.4(HOXD10):c.*234AT[8]AAA[1]	HOXD10	Microsatellite (3 prime UTR variant)	not provided	GLikely benign
Select item 332505	NM_002148.4(HOXD10):c.*468A>T	HOXD10	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GConflicting classifications of pathogenicity