ClinVar Miner

List of variants in gene IFNA10 studied for not specified

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_002171.2(IFNA10):c.437A>C (p.Tyr146Ser) rs139697457 0.00073
NM_002171.2(IFNA10):c.114G>T (p.Leu38Phe) rs138686794 0.00046
NM_002171.2(IFNA10):c.205A>C (p.Asn69His) rs1062570 0.00046
NM_002171.2(IFNA10):c.519A>T (p.Arg173Ser) rs141756650 0.00046
NM_002171.2(IFNA10):c.565G>A (p.Asp189Asn) rs149261728 0.00039
NM_002171.2(IFNA10):c.152C>G (p.Ser51Cys) rs545860454 0.00028
NM_002171.2(IFNA10):c.280G>A (p.Glu94Lys) rs146907935 0.00015
NM_002171.2(IFNA10):c.398C>A (p.Pro133His) rs369916950 0.00014
NM_002171.2(IFNA10):c.385G>A (p.Val129Met) rs542010952 0.00007
NM_002171.2(IFNA10):c.215A>G (p.Gln72Arg) rs781635594 0.00006
NM_002171.2(IFNA10):c.410A>T (p.Glu137Val) rs559723085 0.00003
NM_002171.2(IFNA10):c.551G>T (p.Arg184Ile) rs748009686 0.00002
NM_002171.2(IFNA10):c.133G>C (p.Gly45Arg) rs763865345 0.00001
NM_002171.2(IFNA10):c.523C>T (p.Leu175Phe) rs553280752 0.00001
NM_002171.2(IFNA10):c.544C>A (p.Gln182Lys) rs1275950936 0.00001
NM_002171.2(IFNA10):c.141C>G (p.Ile47Met) rs1238121993
NM_002171.2(IFNA10):c.143C>G (p.Ser48Cys) rs746398984
NM_002171.2(IFNA10):c.150C>A (p.Phe50Leu)
NM_002171.2(IFNA10):c.194A>T (p.Glu65Val)
NM_002171.2(IFNA10):c.199G>A (p.Asp67Asn) rs748350258
NM_002171.2(IFNA10):c.362C>T (p.Ala121Val)
NM_002171.2(IFNA10):c.391G>C (p.Glu131Gln)
NM_002171.2(IFNA10):c.394A>G (p.Thr132Ala)
NM_002171.2(IFNA10):c.395C>T (p.Thr132Ile)
NM_002171.2(IFNA10):c.397C>G (p.Pro133Ala)
NM_002171.2(IFNA10):c.403A>T (p.Met135Leu) rs2537264408
NM_002171.2(IFNA10):c.439T>G (p.Phe147Val)
NM_002171.2(IFNA10):c.43A>C (p.Ser15Arg) rs2537265088
NM_002171.2(IFNA10):c.452C>T (p.Thr151Ile)
NM_002171.2(IFNA10):c.460C>G (p.Leu154Val)
NM_002171.2(IFNA10):c.480C>A (p.Ser160Arg)
NM_002171.2(IFNA10):c.480C>G (p.Ser160Arg)
NM_002171.2(IFNA10):c.527C>T (p.Ser176Leu) rs762249251
NM_002171.2(IFNA10):c.71G>C (p.Cys24Ser)

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