ClinVar Miner

List of variants in gene combination C1orf105, PIGC

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Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_153747.2(PIGC):c.267T>C (p.Gly89=) rs2230471 0.85989
NM_153747.2(PIGC):c.796C>T (p.Pro266Ser) rs1063412 0.44041
NM_153747.2(PIGC):c.676C>T (p.Arg226Trp) rs34001453 0.00635
NM_153747.2(PIGC):c.498T>C (p.Tyr166=) rs138512059 0.00451
NM_153747.2(PIGC):c.393T>C (p.Tyr131=) rs61747502 0.00111
NM_153747.2(PIGC):c.389C>T (p.Thr130Ile) rs146481462 0.00043
NM_153747.2(PIGC):c.308T>C (p.Ile103Thr) rs61747503 0.00031
NM_153747.2(PIGC):c.61C>T (p.Arg21Ter) rs115209243 0.00031
NM_153747.2(PIGC):c.445A>G (p.Ile149Val) rs200105210 0.00021
NM_153747.2(PIGC):c.119A>G (p.Asn40Ser) rs779814454 0.00009
NM_153747.2(PIGC):c.812G>A (p.Arg271His) rs370905635 0.00008
NM_153747.2(PIGC):c.113G>A (p.Arg38Gln) rs201429163 0.00007
NM_153747.2(PIGC):c.739A>G (p.Ser247Gly) rs751068367 0.00004
NM_153747.2(PIGC):c.574C>T (p.Arg192Cys) rs768479943 0.00001
NM_153747.2(PIGC):c.635T>C (p.Leu212Pro) rs1553259602 0.00001
GRCh37/hg19 1q24.3(chr1:172399416-172468762)x1
NC_000001.10:g.(?_172410869)_(172411762_?)dup
NM_153747.2(PIGC):c.112C>T (p.Arg38Trp)
NM_153747.2(PIGC):c.126T>C (p.His42=)
NM_153747.2(PIGC):c.12_13insTTGTGACTAACA (p.Pro5delinsLeuTer)
NM_153747.2(PIGC):c.138C>A (p.Tyr46Ter) rs375570541
NM_153747.2(PIGC):c.13C>A (p.Pro5Thr)
NM_153747.2(PIGC):c.16G>A (p.Val6Met)
NM_153747.2(PIGC):c.193G>A (p.Val65Ile)
NM_153747.2(PIGC):c.223A>G (p.Met75Val)
NM_153747.2(PIGC):c.225G>A (p.Met75Ile)
NM_153747.2(PIGC):c.247C>T (p.His83Tyr)
NM_153747.2(PIGC):c.256T>A (p.Leu86Ile) rs2149169681
NM_153747.2(PIGC):c.266G>A (p.Gly89Asp) rs1647406021
NM_153747.2(PIGC):c.275C>A (p.Ser92Tyr)
NM_153747.2(PIGC):c.286G>A (p.Gly96Arg)
NM_153747.2(PIGC):c.325C>T (p.Arg109Trp)
NM_153747.2(PIGC):c.330G>T (p.Lys110Asn)
NM_153747.2(PIGC):c.336T>C (p.Ser112=)
NM_153747.2(PIGC):c.36C>G (p.Val12=)
NM_153747.2(PIGC):c.411G>A (p.Leu137=)
NM_153747.2(PIGC):c.484A>T (p.Ile162Phe)
NM_153747.2(PIGC):c.530T>C (p.Leu177Pro)
NM_153747.2(PIGC):c.531A>G (p.Leu177=)
NM_153747.2(PIGC):c.533C>T (p.Ser178Phe)
NM_153747.2(PIGC):c.557C>G (p.Ser186Cys)
NM_153747.2(PIGC):c.566T>G (p.Leu189Trp) rs1553259614
NM_153747.2(PIGC):c.580C>A (p.Pro194Thr)
NM_153747.2(PIGC):c.584G>A (p.Arg195Gln)
NM_153747.2(PIGC):c.593A>G (p.His198Arg)
NM_153747.2(PIGC):c.605T>G (p.Met202Arg)
NM_153747.2(PIGC):c.635T>G (p.Leu212Arg)
NM_153747.2(PIGC):c.644T>C (p.Met215Thr)
NM_153747.2(PIGC):c.659T>C (p.Leu220Pro) rs786205667
NM_153747.2(PIGC):c.677G>A (p.Arg226Gln)
NM_153747.2(PIGC):c.68C>T (p.Pro23Leu)
NM_153747.2(PIGC):c.70T>C (p.Phe24Leu)
NM_153747.2(PIGC):c.734C>G (p.Ser245Cys)
NM_153747.2(PIGC):c.770T>C (p.Leu257Pro)
NM_153747.2(PIGC):c.791T>C (p.Leu264Pro)
NM_153747.2(PIGC):c.83A>G (p.Tyr28Cys)
NM_153747.2(PIGC):c.84T>C (p.Tyr28=)
NM_153747.2(PIGC):c.850G>A (p.Asp284Asn)
NM_153747.2(PIGC):c.859G>T (p.Glu287Ter)
NM_153747.2(PIGC):c.861A>G (p.Glu287=)
NM_153747.2(PIGC):c.865A>C (p.Lys289Gln)
NM_153747.2(PIGC):c.881G>T (p.Arg294Met)
NM_153747.2(PIGC):c.91C>T (p.Arg31Trp)
NM_153747.2(PIGC):c.94C>A (p.Arg32=)

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