List of variants in gene HOXD10 reported as uncertain significance for congenital deformities of limbs

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_002148.4(HOXD10):c.*235A>T	rs76652386	0.00942
NM_002148.4(HOXD10):c.*468A>T	rs532592274	0.00271
NM_002148.4(HOXD10):c.*233T>A	rs867263804	0.00045
NM_002148.4(HOXD10):c.*278G>A	rs565659273	0.00044
NM_002148.4(HOXD10):c.*270G>A	rs779201977	0.00034
NM_002148.4(HOXD10):c.*208A>G	rs867143553	0.00008
NM_002148.4(HOXD10):c.266G>A (p.Arg89Gln)	rs374700658	0.00005
NM_002148.4(HOXD10):c.420C>G (p.Pro140=)	rs375702128	0.00005
NM_002148.4(HOXD10):c.-6C>G	rs538359875	0.00001
NM_002148.4(HOXD10):c.561G>A (p.Lys187=)	rs143870330	0.00001
NM_002148.4(HOXD10):c.*205TA[13]	rs6147035
NM_002148.4(HOXD10):c.*205TA[14]	rs6147035
NM_002148.4(HOXD10):c.*205TA[17]	rs6147035
NM_002148.4(HOXD10):c.*205TA[18]	rs6147035
NM_002148.4(HOXD10):c.*205TA[21]	rs6147035
NM_002148.4(HOXD10):c.*205TA[23]	rs6147035
NM_002148.4(HOXD10):c.*21C>T	rs570165195
NM_002148.4(HOXD10):c.*235delinsTATATATATAT	rs886055161
NM_002148.4(HOXD10):c.*235delinsTATATATATATATATAT	rs886055161
NM_002148.4(HOXD10):c.*34G>A	rs1689824324
NM_002148.4(HOXD10):c.*76G>C	rs558709855
NM_002148.4(HOXD10):c.*83G>A	rs1008365837
NM_002148.4(HOXD10):c.-10C>A	rs781377305
NM_002148.4(HOXD10):c.116C>T (p.Pro39Leu)	rs886055157
NM_002148.4(HOXD10):c.341G>T (p.Cys114Phe)
NM_002148.4(HOXD10):c.543C>A (p.Asn181Lys)	rs886055158
NM_002148.4(HOXD10):c.684G>C (p.Glu228Asp)	rs1378675941
NM_002148.4(HOXD10):c.753C>G (p.Ile251Met)
NM_002148.4(HOXD10):c.786T>A (p.Thr262=)	rs755118732
NM_002148.4(HOXD10):c.87C>T (p.Ser29=)	rs752887490

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