ClinVar Miner

List of variants in gene CTDP1 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_004715.5(CTDP1):c.2817T>C (p.Asp939=) rs626169 0.90284
NM_004715.5(CTDP1):c.863+398C>T rs676713 0.76142
NM_004715.5(CTDP1):c.181T>G (p.Ser61Ala) rs17855830 0.63679
NM_004715.5(CTDP1):c.2069-20C>T rs8084175 0.12733
NM_004715.5(CTDP1):c.1019C>T (p.Thr340Met) rs2279103 0.12725
NM_004715.5(CTDP1):c.1066T>C (p.Ser356Pro) rs139598569 0.00322
NM_004715.5(CTDP1):c.2223T>C (p.Pro741=) rs77320492 0.00184
NM_004715.5(CTDP1):c.294G>A (p.Pro98=) rs187756055 0.00138
NM_004715.5(CTDP1):c.780A>G (p.Leu260=) rs148352897 0.00113
NM_004715.5(CTDP1):c.863+10C>T rs375464090 0.00099
NM_004715.5(CTDP1):c.2323G>A (p.Asp775Asn) rs145870152 0.00038
NM_004715.5(CTDP1):c.2727G>A (p.Ala909=) rs142544366 0.00035
NM_004715.5(CTDP1):c.1626C>T (p.Cys542=) rs141075287 0.00023
NM_004715.5(CTDP1):c.669G>A (p.Thr223=) rs146831211 0.00017
NM_004715.5(CTDP1):c.2028C>T (p.Asp676=) rs369463770 0.00006
NM_004715.5(CTDP1):c.2217C>T (p.Asn739=) rs142525132 0.00005
NM_004715.5(CTDP1):c.-5C>T
NM_004715.5(CTDP1):c.1290G>A (p.Ala430=)
NM_004715.5(CTDP1):c.1338G>A (p.Thr446=)
NM_004715.5(CTDP1):c.1341C>A (p.Gly447=)
NM_004715.5(CTDP1):c.1419C>G (p.Ala473=)
NM_004715.5(CTDP1):c.1487C>T (p.Ala496Val)
NM_004715.5(CTDP1):c.1543G>A (p.Gly515Arg)
NM_004715.5(CTDP1):c.1692G>A (p.Ser564=)
NM_004715.5(CTDP1):c.1829G>A (p.Arg610His)
NM_004715.5(CTDP1):c.1938G>A (p.Pro646=)
NM_004715.5(CTDP1):c.1987C>T (p.Leu663=)
NM_004715.5(CTDP1):c.2055C>T (p.Ile685=)
NM_004715.5(CTDP1):c.2259C>T (p.Thr753=)
NM_004715.5(CTDP1):c.2421G>A (p.Ala807=)
NM_004715.5(CTDP1):c.2439G>A (p.Pro813=)
NM_004715.5(CTDP1):c.2535G>A (p.Pro845=)
NM_004715.5(CTDP1):c.384C>G (p.Gly128=)
NM_004715.5(CTDP1):c.492+8G>T rs187068493
NM_004715.5(CTDP1):c.591C>T (p.Thr197=)
NM_004715.5(CTDP1):c.759A>G (p.Ala253=)
NM_004715.5(CTDP1):c.864-3T>C

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