ClinVar Miner

List of variants in gene CTDP1 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 85
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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.492+102A>G rs655609 0.77264
NM_004715.5(CTDP1):c.1031-263T>C rs529195 0.76265
NM_004715.5(CTDP1):c.773-224A>G rs517479 0.76121
NM_004715.5(CTDP1):c.2747+156C>A rs4799081 0.72898
NM_004715.5(CTDP1):c.181T>G (p.Ser61Ala) rs17855830 0.63679
NM_004715.5(CTDP1):c.399-106C>T rs558700 0.51813
NM_004715.5(CTDP1):c.-104G>T rs56006341 0.30556
NM_004715.5(CTDP1):c.2069-156G>A rs2242177 0.30445
NM_004715.5(CTDP1):c.621+49T>C rs2242174 0.30311
NM_004715.5(CTDP1):c.2580+100G>A rs9956086 0.24410
NM_004715.5(CTDP1):c.978G>A (p.Thr326=) rs599554 0.20817
NM_004715.5(CTDP1):c.1461G>A (p.Pro487=) rs2126082 0.18278
NC_000018.10:g.79679756G>A rs56246515 0.17751
NM_004715.5(CTDP1):c.*51G>A rs76088733 0.17237
NM_004715.5(CTDP1):c.2748-157C>T rs578051 0.16112
NM_004715.5(CTDP1):c.398+269C>T rs898619 0.15399
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.492+153G>A rs55781531 0.12608
NM_004715.5(CTDP1):c.2417+150G>A rs55830009 0.12205
NM_004715.5(CTDP1):c.2068+131A>G rs76553883 0.07791
NM_004715.5(CTDP1):c.186G>C (p.Gly62=) rs79644263 0.05976
NM_004715.5(CTDP1):c.314+100C>T rs113762153 0.05750
NM_004715.5(CTDP1):c.863+15G>A rs62097743 0.04726
NM_004715.5(CTDP1):c.315-109G>A rs112726648 0.04260
NM_004715.5(CTDP1):c.1995G>A (p.Ala665=) rs11549119 0.03715
NM_004715.5(CTDP1):c.2412C>T (p.Ser804=) rs35456241 0.03715
NM_004715.5(CTDP1):c.863+247G>A rs186289786 0.03543
NM_004715.5(CTDP1):c.622-132C>T rs113114336 0.03108
NM_004715.5(CTDP1):c.2580+255G>A rs115803470 0.02324
NM_004715.5(CTDP1):c.317C>T (p.Ala106Val) rs115044443 0.02310
NM_004715.5(CTDP1):c.729C>T (p.His243=) rs35925235 0.02230
NM_004715.5(CTDP1):c.621+184T>C rs116739591 0.02078
NM_004715.5(CTDP1):c.398+210C>T rs112906035 0.02077
NM_004715.5(CTDP1):c.492+228G>A rs112570447 0.02076
NM_004715.5(CTDP1):c.315-225G>C rs115564654 0.01910
NM_004715.5(CTDP1):c.492+7C>T rs115851227 0.01593
NM_004715.5(CTDP1):c.772+276G>A rs112301532 0.01537
NM_004715.5(CTDP1):c.772+114A>G rs113399282 0.01533
NM_004715.5(CTDP1):c.2241G>C (p.Arg747=) rs151072597 0.01353
NM_004715.5(CTDP1):c.1166C>T (p.Ala389Val) rs144647072 0.00968
NM_004715.5(CTDP1):c.213G>C (p.Gly71=) rs201234471 0.00821
NM_004715.5(CTDP1):c.150C>G (p.Ala50=) rs564311662 0.00730
NM_004715.5(CTDP1):c.621+17T>C rs112822941 0.00724
NM_004715.5(CTDP1):c.1908C>T (p.Asp636=) rs143177926 0.00515
NM_004715.5(CTDP1):c.2068+45G>C rs79257976 0.00493
NM_004715.5(CTDP1):c.2264T>C (p.Leu755Ser) rs34967023 0.00489
NM_004715.5(CTDP1):c.708C>T (p.Ile236=) rs139050858 0.00468
NM_004715.5(CTDP1):c.1251A>G (p.Gln417=) rs34942031 0.00447
NM_004715.5(CTDP1):c.1602G>T (p.Glu534Asp) rs112655649 0.00349
NM_004715.5(CTDP1):c.1066T>C (p.Ser356Pro) rs139598569 0.00322
NM_004715.5(CTDP1):c.1311G>A (p.Pro437=) rs373108713 0.00296
NM_004715.5(CTDP1):c.2274G>A (p.Pro758=) rs140627086 0.00288
NM_004715.5(CTDP1):c.2070C>T (p.Gly690=) rs145726709 0.00262
NM_004715.5(CTDP1):c.2322C>T (p.Tyr774=) rs35234657 0.00242
NM_004715.5(CTDP1):c.2581-5G>T rs199505565 0.00239
NM_004715.5(CTDP1):c.2748-4G>T rs140538707 0.00227
NM_004715.5(CTDP1):c.2223T>C (p.Pro741=) rs77320492 0.00184
NM_004715.5(CTDP1):c.786C>T (p.Pro262=) rs140645111 0.00139
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.2069-14C>T rs199774811 0.00099
NM_004715.5(CTDP1):c.863+10C>T rs375464090 0.00099
NM_004715.5(CTDP1):c.2742G>T (p.Gly914=) rs145979721 0.00060
NM_004715.5(CTDP1):c.1056C>G (p.Val352=) rs147146455 0.00050
NM_004715.5(CTDP1):c.14C>A (p.Ala5Asp) rs571765834 0.00023
NM_004715.5(CTDP1):c.1626C>T (p.Cys542=) rs141075287 0.00023
NM_004715.5(CTDP1):c.2190C>T (p.Asp730=) rs150792349 0.00016
NM_004715.5(CTDP1):c.153G>C (p.Val51=) rs751687521 0.00001
NM_004715.5(CTDP1):c.1728GGA[8] (p.Glu582dup) rs3833180
NM_004715.5(CTDP1):c.2069-163C>G rs676367
NM_004715.5(CTDP1):c.2069-7C>T
NM_004715.5(CTDP1):c.225C>T (p.Arg75=)
NM_004715.5(CTDP1):c.2747+234del rs10709142
NM_004715.5(CTDP1):c.2748-187G>A rs8086389
NM_004715.5(CTDP1):c.314+7111G>T
NM_004715.5(CTDP1):c.315-4G>A
NM_004715.5(CTDP1):c.315-5dup
NM_004715.5(CTDP1):c.375T>C (p.Ala125=)
NM_004715.5(CTDP1):c.399-287C>T rs70198
NM_004715.5(CTDP1):c.492+8G>T rs187068493
NM_004715.5(CTDP1):c.492+91G>A rs58480469
NM_004715.5(CTDP1):c.622-273T>G rs113786741
NM_004715.5(CTDP1):c.864-7C>T

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