| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.39999458G>A | CA367288332 | CDK13 | c.2140G>A (p.Gly714Ser) c.692G>A n.622G>A c.1031G>A c.454G>A (p.Gly152Ser) c.70G>A (p.Gly24Ser) c.1480G>A (p.Gly494Ser) n.1209G>A n.3977G>A n.692G>A c.298G>A (p.Gly100Ser) | COSMIC |
| 7 | g.39999458G>C | CA16044433 | CDK13 | c.2140G>C (p.Gly714Arg) c.692G>C n.622G>C c.1031G>C c.454G>C (p.Gly152Arg) c.70G>C (p.Gly24Arg) c.1480G>C (p.Gly494Arg) n.1209G>C n.3977G>C n.692G>C c.298G>C (p.Gly100Arg) | ClinVar dbSNP |
| 7 | g.39999458G= | CA1701738265 | CDK13 | c.2140G= (p.Gly714=) c.692G= n.622G= c.1031G= c.454G= (p.Gly152=) c.70G= (p.Gly24=) c.1480G= (p.Gly494=) n.1209G= n.3977G= n.692G= c.298G= (p.Gly100=) | |
| 7 | g.39999458G>T | CA367288335 | CDK13 | c.2140G>T (p.Gly714Cys) c.692G>T n.622G>T c.1031G>T c.454G>T (p.Gly152Cys) c.70G>T (p.Gly24Cys) c.1480G>T (p.Gly494Cys) n.1209G>T n.3977G>T n.692G>T c.298G>T (p.Gly100Cys) | ClinVar |
| 7 | g.39999459G>A | CA367288336 | CDK13 | c.2141G>A (p.Gly714Asp) c.693G>A n.623G>A c.1032G>A c.455G>A (p.Gly152Asp) c.71G>A (p.Gly24Asp) c.1481G>A (p.Gly494Asp) n.1210G>A n.3978G>A n.693G>A c.299G>A (p.Gly100Asp) | ClinVar |
| 7 | g.39999459G>C | CA367288337 | CDK13 | c.2141G>C (p.Gly714Ala) c.693G>C n.623G>C c.1032G>C c.455G>C (p.Gly152Ala) c.71G>C (p.Gly24Ala) c.1481G>C (p.Gly494Ala) n.1210G>C n.3978G>C n.693G>C c.299G>C (p.Gly100Ala) | |
| 7 | g.39999459G>T | CA367288339 | CDK13 | c.2141G>T (p.Gly714Val) c.693G>T n.623G>T c.1032G>T c.455G>T (p.Gly152Val) c.71G>T (p.Gly24Val) c.1481G>T (p.Gly494Val) n.1210G>T n.3978G>T n.693G>T c.299G>T (p.Gly100Val) | ClinVar |
| 7 | g.39999460T>A | CA454724015 | CDK13 | c.2142T>A (p.Gly714=) c.694T>A n.624T>A c.1033T>A c.456T>A (p.Gly152=) c.72T>A (p.Gly24=) c.1482T>A (p.Gly494=) n.1211T>A n.3979T>A n.694T>A c.300T>A (p.Gly100=) | |
| 7 | g.39999460T>C | CA454724016 | CDK13 | c.2142T>C (p.Gly714=) c.694T>C n.624T>C c.1033T>C c.456T>C (p.Gly152=) c.72T>C (p.Gly24=) c.1482T>C (p.Gly494=) n.1211T>C n.3979T>C n.694T>C c.300T>C (p.Gly100=) | dbSNP gnomAD v4 |
| 7 | g.39999460T>G | CA454724017 | CDK13 | c.2142T>G (p.Gly714=) c.694T>G n.624T>G c.1033T>G c.456T>G (p.Gly152=) c.72T>G (p.Gly24=) c.1482T>G (p.Gly494=) n.1211T>G n.3979T>G n.694T>G c.300T>G (p.Gly100=) | |
| 7 | g.39999460T= | CA1701738266 | CDK13 | c.2142T= (p.Gly714=) c.694T= n.624T= c.1033T= c.456T= (p.Gly152=) c.72T= (p.Gly24=) c.1482T= (p.Gly494=) n.1211T= n.3979T= n.694T= c.300T= (p.Gly100=) | |
| 7 | g.39999461A>C | CA367288352 | CDK13 | c.2143A>C (p.Thr715Pro) c.695A>C n.625A>C c.1034A>C c.457A>C (p.Thr153Pro) c.73A>C (p.Thr25Pro) c.1483A>C (p.Thr495Pro) n.1212A>C n.3980A>C n.695A>C c.301A>C (p.Thr101Pro) | |
| 7 | g.39999461A>G | CA367288353 | CDK13 | c.2143A>G (p.Thr715Ala) c.695A>G n.625A>G c.1034A>G c.457A>G (p.Thr153Ala) c.73A>G (p.Thr25Ala) c.1483A>G (p.Thr495Ala) n.1212A>G n.3980A>G n.695A>G c.301A>G (p.Thr101Ala) | |
| 7 | g.39999461A>T | CA367288354 | CDK13 | c.2143A>T (p.Thr715Ser) c.695A>T n.625A>T c.1034A>T c.457A>T (p.Thr153Ser) c.73A>T (p.Thr25Ser) c.1483A>T (p.Thr495Ser) n.1212A>T n.3980A>T n.695A>T c.301A>T (p.Thr101Ser) | |
| 7 | g.39999462C>A | CA367288356 | CDK13 | c.2144C>A (p.Thr715Asn) c.696C>A n.626C>A c.1035C>A c.458C>A (p.Thr153Asn) c.74C>A (p.Thr25Asn) c.1484C>A (p.Thr495Asn) n.1213C>A n.3981C>A n.696C>A c.302C>A (p.Thr101Asn) | |
| 7 | g.39999462C>G | CA367288358 | CDK13 | c.2144C>G (p.Thr715Ser) c.696C>G n.626C>G c.1035C>G c.458C>G (p.Thr153Ser) c.74C>G (p.Thr25Ser) c.1484C>G (p.Thr495Ser) n.1213C>G n.3981C>G n.696C>G c.302C>G (p.Thr101Ser) | |
| 7 | g.39999462C>T | CA367288359 | CDK13 | c.2144C>T (p.Thr715Ile) c.696C>T n.626C>T c.1035C>T c.458C>T (p.Thr153Ile) c.74C>T (p.Thr25Ile) c.1484C>T (p.Thr495Ile) n.1213C>T n.3981C>T n.696C>T c.302C>T (p.Thr101Ile) | |
| 7 | g.39999463T>A | CA454724018 | CDK13 | c.2145T>A (p.Thr715=) c.697T>A n.627T>A c.1036T>A c.459T>A (p.Thr153=) c.75T>A (p.Thr25=) c.1485T>A (p.Thr495=) n.1214T>A n.3982T>A n.697T>A c.303T>A (p.Thr101=) | |
| 7 | g.39999463T>C | CA454724019 | CDK13 | c.2145T>C (p.Thr715=) c.697T>C n.627T>C c.1036T>C c.459T>C (p.Thr153=) c.75T>C (p.Thr25=) c.1485T>C (p.Thr495=) n.1214T>C n.3982T>C n.697T>C c.303T>C (p.Thr101=) | |
| 7 | g.39999463T>G | CA454724020 | CDK13 | c.2145T>G (p.Thr715=) c.697T>G n.627T>G c.1036T>G c.459T>G (p.Thr153=) c.75T>G (p.Thr25=) c.1485T>G (p.Thr495=) n.1214T>G n.3982T>G n.697T>G c.303T>G (p.Thr101=) | |
| 7 | g.39999464T>A | CA367288363 | CDK13 | c.2146T>A (p.Tyr716Asn) c.698T>A n.628T>A c.1037T>A c.460T>A (p.Tyr154Asn) c.76T>A (p.Tyr26Asn) c.1486T>A (p.Tyr496Asn) n.1215T>A n.3983T>A n.698T>A c.304T>A (p.Tyr102Asn) | |
| 7 | g.39999464T>C | CA367288364 | CDK13 | c.2146T>C (p.Tyr716His) c.698T>C n.628T>C c.1037T>C c.460T>C (p.Tyr154His) c.76T>C (p.Tyr26His) c.1486T>C (p.Tyr496His) n.1215T>C n.3983T>C n.698T>C c.304T>C (p.Tyr102His) | |
| 7 | g.39999464T>G | CA367288361 | CDK13 | c.2146T>G (p.Tyr716Asp) c.698T>G n.628T>G c.1037T>G c.460T>G (p.Tyr154Asp) c.76T>G (p.Tyr26Asp) c.1486T>G (p.Tyr496Asp) n.1215T>G n.3983T>G n.698T>G c.304T>G (p.Tyr102Asp) | |
| 7 | g.39999464T= | CA1701738267 | CDK13 | c.2146T= (p.Tyr716=) c.698T= n.628T= c.1037T= c.460T= (p.Tyr154=) c.76T= (p.Tyr26=) c.1486T= (p.Tyr496=) n.1215T= n.3983T= n.698T= c.304T= (p.Tyr102=) | |
| 7 | g.39999465A>C | CA367288365 | CDK13 | c.2147A>C (p.Tyr716Ser) c.699A>C n.629A>C c.1038A>C c.461A>C (p.Tyr154Ser) c.77A>C (p.Tyr26Ser) c.1487A>C (p.Tyr496Ser) n.1216A>C n.3984A>C n.699A>C c.305A>C (p.Tyr102Ser) | |
| 7 | g.39999465A>G | CA367288371 | CDK13 | c.2147A>G (p.Tyr716Cys) c.699A>G n.629A>G c.1038A>G c.461A>G (p.Tyr154Cys) c.77A>G (p.Tyr26Cys) c.1487A>G (p.Tyr496Cys) n.1216A>G n.3984A>G n.699A>G c.305A>G (p.Tyr102Cys) | |
| 7 | g.39999465A>T | CA367288366 | CDK13 | c.2147A>T (p.Tyr716Phe) c.699A>T n.629A>T c.1038A>T c.461A>T (p.Tyr154Phe) c.77A>T (p.Tyr26Phe) c.1487A>T (p.Tyr496Phe) n.1216A>T n.3984A>T n.699A>T c.305A>T (p.Tyr102Phe) | |
| 7 | g.39999465dup | CA4228642 | CDK13 | c.2147dup (p.Tyr716Ter) c.699dup n.629dup c.1038dup c.461dup (p.Tyr154Ter) c.77dup (p.Tyr26Ter) c.1487dup (p.Tyr496Ter) n.1216dup n.3984dup n.699dup c.305dup (p.Tyr102Ter) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.39999466C>A | CA367288374 | CDK13 | c.2148C>A (p.Tyr716Ter) c.700C>A n.630C>A c.1039C>A c.462C>A (p.Tyr154Ter) c.78C>A (p.Tyr26Ter) c.1488C>A (p.Tyr496Ter) n.1217C>A n.3985C>A n.700C>A c.306C>A (p.Tyr102Ter) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.39999466C= | CA1701738268 | CDK13 | c.2148C= (p.Tyr716=) c.700C= n.630C= c.1039C= c.462C= (p.Tyr154=) c.78C= (p.Tyr26=) c.1488C= (p.Tyr496=) n.1217C= n.3985C= n.700C= c.306C= (p.Tyr102=) | |
| 7 | g.39999466C>G | CA367288376 | CDK13 | c.2148C>G (p.Tyr716Ter) c.700C>G n.630C>G c.1039C>G c.462C>G (p.Tyr154Ter) c.78C>G (p.Tyr26Ter) c.1488C>G (p.Tyr496Ter) n.1217C>G n.3985C>G n.700C>G c.306C>G (p.Tyr102Ter) | |
| 7 | g.39999466C>T | CA4228643 | CDK13 | c.2148C>T (p.Tyr716=) c.700C>T n.630C>T c.1039C>T c.462C>T (p.Tyr154=) c.78C>T (p.Tyr26=) c.1488C>T (p.Tyr496=) n.1217C>T n.3985C>T n.700C>T c.306C>T (p.Tyr102=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.39999467G>A | CA16044432 | CDK13 | c.2149G>A (p.Gly717Arg) c.701G>A n.631G>A c.1040G>A c.463G>A (p.Gly155Arg) c.79G>A (p.Gly27Arg) c.1489G>A (p.Gly497Arg) n.1218G>A n.3986G>A n.701G>A c.307G>A (p.Gly103Arg) | ClinVar dbSNP gnomAD v4 |
| 7 | g.39999467G>C | CA367288382 | CDK13 | c.2149G>C (p.Gly717Arg) c.701G>C n.631G>C c.1040G>C c.463G>C (p.Gly155Arg) c.79G>C (p.Gly27Arg) c.1489G>C (p.Gly497Arg) n.1218G>C n.3986G>C n.701G>C c.307G>C (p.Gly103Arg) | |
| 7 | g.39999467G= | CA1701738269 | CDK13 | c.2149G= (p.Gly717=) c.701G= n.631G= c.1040G= c.463G= (p.Gly155=) c.79G= (p.Gly27=) c.1489G= (p.Gly497=) n.1218G= n.3986G= n.701G= c.307G= (p.Gly103=) | |
| 7 | g.39999467G>T | CA367288389 | CDK13 | c.2149G>T (p.Gly717Ter) c.701G>T n.631G>T c.1040G>T c.463G>T (p.Gly155Ter) c.79G>T (p.Gly27Ter) c.1489G>T (p.Gly497Ter) n.1218G>T n.3986G>T n.701G>T c.307G>T (p.Gly103Ter) | |
| 7 | g.39999468G>A | CA367288392 | CDK13 | c.2150G>A (p.Gly717Glu) c.702G>A n.632G>A c.1041G>A c.464G>A (p.Gly155Glu) c.80G>A (p.Gly27Glu) c.1490G>A (p.Gly497Glu) n.1219G>A n.3987G>A n.702G>A c.308G>A (p.Gly103Glu) | dbSNP |
| 7 | g.39999468G>C | CA367288395 | CDK13 | c.2150G>C (p.Gly717Ala) c.702G>C n.632G>C c.1041G>C c.464G>C (p.Gly155Ala) c.80G>C (p.Gly27Ala) c.1490G>C (p.Gly497Ala) n.1219G>C n.3987G>C n.702G>C c.308G>C (p.Gly103Ala) | |
| 7 | g.39999468G>T | CA367288397 | CDK13 | c.2150G>T (p.Gly717Val) c.702G>T n.632G>T c.1041G>T c.464G>T (p.Gly155Val) c.80G>T (p.Gly27Val) c.1490G>T (p.Gly497Val) n.1219G>T n.3987G>T n.702G>T c.308G>T (p.Gly103Val) | |
| 7 | g.39999469A>C | CA454724022 | CDK13 | c.2151A>C (p.Gly717=) c.703A>C n.633A>C c.1042A>C c.465A>C (p.Gly155=) c.81A>C (p.Gly27=) c.1491A>C (p.Gly497=) n.1220A>C n.3988A>C n.703A>C c.309A>C (p.Gly103=) | |
| 7 | g.39999469A>G | CA454724023 | CDK13 | c.2151A>G (p.Gly717=) c.703A>G n.633A>G c.1042A>G c.465A>G (p.Gly155=) c.81A>G (p.Gly27=) c.1491A>G (p.Gly497=) n.1220A>G n.3988A>G n.703A>G c.309A>G (p.Gly103=) | gnomAD v4 |
| 7 | g.39999469A>T | CA454724024 | CDK13 | c.2151A>T (p.Gly717=) c.703A>T n.633A>T c.1042A>T c.465A>T (p.Gly155=) c.81A>T (p.Gly27=) c.1491A>T (p.Gly497=) n.1220A>T n.3988A>T n.703A>T c.309A>T (p.Gly103=) | |
| 7 | g.39999470C>A | CA367288398 | CDK13 | c.2152C>A (p.Gln718Lys) c.704C>A n.634C>A c.1043C>A c.466C>A (p.Gln156Lys) c.82C>A (p.Gln28Lys) c.1492C>A (p.Gln498Lys) n.1221C>A n.3989C>A n.704C>A c.310C>A (p.Gln104Lys) | |
| 7 | g.39999470C= | CA1701738270 | CDK13 | c.2152C= (p.Gln718=) c.704C= n.634C= c.1043C= c.466C= (p.Gln156=) c.82C= (p.Gln28=) c.1492C= (p.Gln498=) n.1221C= n.3989C= n.704C= c.310C= (p.Gln104=) | |
| 7 | g.39999470C>G | CA367288399 | CDK13 | c.2152C>G (p.Gln718Glu) c.704C>G n.634C>G c.1043C>G c.466C>G (p.Gln156Glu) c.82C>G (p.Gln28Glu) c.1492C>G (p.Gln498Glu) n.1221C>G n.3989C>G n.704C>G c.310C>G (p.Gln104Glu) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.39999470C>T | CA367288401 | CDK13 | c.2152C>T (p.Gln718Ter) c.704C>T n.634C>T c.1043C>T c.466C>T (p.Gln156Ter) c.82C>T (p.Gln28Ter) c.1492C>T (p.Gln498Ter) n.1221C>T n.3989C>T n.704C>T c.310C>T (p.Gln104Ter) | |
| 7 | g.39999471A>C | CA367288406 | CDK13 | c.2153A>C (p.Gln718Pro) c.705A>C n.635A>C c.1044A>C c.467A>C (p.Gln156Pro) c.83A>C (p.Gln28Pro) c.1493A>C (p.Gln498Pro) n.1222A>C n.3990A>C n.705A>C c.311A>C (p.Gln104Pro) | |
| 7 | g.39999471A>G | CA367288403 | CDK13 | c.2153A>G (p.Gln718Arg) c.705A>G n.635A>G c.1044A>G c.467A>G (p.Gln156Arg) c.83A>G (p.Gln28Arg) c.1493A>G (p.Gln498Arg) n.1222A>G n.3990A>G n.705A>G c.311A>G (p.Gln104Arg) | |
| 7 | g.39999471A>T | CA367288404 | CDK13 | c.2153A>T (p.Gln718Leu) c.705A>T n.635A>T c.1044A>T c.467A>T (p.Gln156Leu) c.83A>T (p.Gln28Leu) c.1493A>T (p.Gln498Leu) n.1222A>T n.3990A>T n.705A>T c.311A>T (p.Gln104Leu) | |
| 7 | g.39999472A= | CA1701738271 | CDK13 | c.2154A= (p.Gln718=) c.706A= n.636A= c.1045A= c.468A= (p.Gln156=) c.84A= (p.Gln28=) c.1494A= (p.Gln498=) n.1223A= n.3991A= n.706A= c.312A= (p.Gln104=) |