ClinVar Miner

List of variants in gene TTLL5 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_015072.5(TTLL5):c.1709-7T>C rs2359870 0.99609
NM_015072.5(TTLL5):c.1187-56G>T rs2288141 0.66272
NM_015072.5(TTLL5):c.446C>T (p.Ala149Val) rs2303345 0.48575
NM_015072.5(TTLL5):c.3800T>C (p.Phe1267Ser) rs1133834 0.30514
NM_015072.5(TTLL5):c.3498G>A (p.Leu1166=) rs3742764 0.13480
NM_015072.5(TTLL5):c.2016-74G>A rs17783198 0.10565
NM_015072.5(TTLL5):c.2136+6G>C rs45480992 0.10133
NM_015072.5(TTLL5):c.265-63T>C rs1477464 0.09139
NM_015072.5(TTLL5):c.934+45A>G rs17783174 0.04401
NM_015072.5(TTLL5):c.2388-12T>C rs72725608 0.02584
NM_015072.5(TTLL5):c.502+69T>G rs77074815 0.02384
NM_015072.5(TTLL5):c.1396-22T>C rs77593112 0.02130
NM_015072.5(TTLL5):c.75-3T>C rs117173802 0.01615
NM_015072.5(TTLL5):c.2232C>T (p.Arg744=) rs2288143 0.01345
NM_015072.5(TTLL5):c.2872A>G (p.Thr958Ala) rs148677697 0.01233
NM_015072.5(TTLL5):c.265-47G>T rs147917101 0.00973
NM_015072.5(TTLL5):c.181+4C>T rs117639142 0.00939
NM_015072.5(TTLL5):c.1186+14T>G rs114107464 0.00898
NM_015072.5(TTLL5):c.2629G>A (p.Ala877Thr) rs112181538 0.00715
NM_015072.5(TTLL5):c.1773C>T (p.Val591=) rs61741261 0.00711
NM_015072.5(TTLL5):c.3544C>T (p.Leu1182=) rs143302131 0.00659
NM_015072.5(TTLL5):c.1395+11G>T rs79846725 0.00603
NM_015072.5(TTLL5):c.2637A>C (p.Leu879Phe) rs146036604 0.00396
NM_015072.5(TTLL5):c.1963C>T (p.Leu655=) rs142427449 0.00320
NM_015072.5(TTLL5):c.2891G>A (p.Arg964Gln) rs142169707 0.00269
NM_015072.5(TTLL5):c.1774G>A (p.Ala592Thr) rs11848004 0.00238
NM_015072.5(TTLL5):c.354A>G (p.Lys118=) rs142072074 0.00185
NM_015072.5(TTLL5):c.576G>T (p.Leu192=) rs556212778 0.00164
NM_015072.5(TTLL5):c.1709-9C>T rs373032875 0.00083
NM_015072.5(TTLL5):c.934+10G>A rs192536539 0.00079
NM_015072.5(TTLL5):c.1576T>C (p.Leu526=) rs2288142 0.00074
NM_015072.5(TTLL5):c.1422G>A (p.Glu474=) rs145268057 0.00065
NM_015072.5(TTLL5):c.740+6A>G rs185044527 0.00060
NM_015072.5(TTLL5):c.824A>G (p.Lys275Arg) rs145430209 0.00046
NM_015072.5(TTLL5):c.2950A>T (p.Ser984Cys) rs141204322 0.00031
NM_015072.5(TTLL5):c.181+18C>T rs546521756 0.00024
NM_015072.5(TTLL5):c.2970C>G (p.Pro990=) rs140291071 0.00017
NM_015072.5(TTLL5):c.2387+11T>A rs747215169 0.00010
NM_015072.5(TTLL5):c.3447A>G (p.Gln1149=) rs140548477 0.00009
NM_015072.5(TTLL5):c.3699C>T (p.His1233=) rs185999044 0.00006
NM_015072.5(TTLL5):c.2603-4A>G rs550463902 0.00001
NM_015072.5(TTLL5):c.3777G>A (p.Gln1259=) rs200369228 0.00001
NM_015072.5(TTLL5):c.1124+68del rs5809726
NM_015072.5(TTLL5):c.1187-20G>A
NM_015072.5(TTLL5):c.1487+24del
NM_015072.5(TTLL5):c.1487+24dup rs200428868
NM_015072.5(TTLL5):c.2136+72del rs57636956
NM_015072.5(TTLL5):c.265-5del rs2140122495
NM_015072.5(TTLL5):c.3522+73G>A rs867363324
NM_015072.5(TTLL5):c.3522+73_3522+74insAAAAAAAA rs869278134
NM_015072.5(TTLL5):c.3522+74_3522+75insA rs1298428665
NM_015072.5(TTLL5):c.3523-5del rs762310604
NM_015072.5(TTLL5):c.3523-5dup rs762310604
NM_015072.5(TTLL5):c.3667G>T (p.Ala1223Ser) rs10130991
NM_015072.5(TTLL5):c.656-3del rs751439234
NM_015072.5(TTLL5):c.656-3dup rs751439234
NM_015072.5(TTLL5):c.656-5_656-3del rs751439234

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