Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.13717397A>C | CA359207112 | DNAH5 | c.12623T>G (p.Ile4208Ser) c.12578T>G (p.Ile4193Ser) c.12731T>G (p.Ile4244Ser) c.11636T>G (p.Ile3879Ser) c.7820T>G (p.Ile2607Ser) c.7373T>G (p.Ile2458Ser) c.6710T>G (p.Ile2237Ser) c.11225T>G (p.Ile3742Ser) | COSMIC |
5 | g.13717397A>G | CA359207085 | DNAH5 | c.12623T>C (p.Ile4208Thr) c.12578T>C (p.Ile4193Thr) c.12731T>C (p.Ile4244Thr) c.11636T>C (p.Ile3879Thr) c.7820T>C (p.Ile2607Thr) c.7373T>C (p.Ile2458Thr) c.6710T>C (p.Ile2237Thr) c.11225T>C (p.Ile3742Thr) | |
5 | g.13717397A>T | CA359207091 | DNAH5 | c.12623T>A (p.Ile4208Asn) c.12578T>A (p.Ile4193Asn) c.12731T>A (p.Ile4244Asn) c.11636T>A (p.Ile3879Asn) c.7820T>A (p.Ile2607Asn) c.7373T>A (p.Ile2458Asn) c.6710T>A (p.Ile2237Asn) c.11225T>A (p.Ile3742Asn) | |
5 | g.13717398T>A | CA359207127 | DNAH5 | c.12622A>T (p.Ile4208Phe) c.12577A>T (p.Ile4193Phe) c.12730A>T (p.Ile4244Phe) c.11635A>T (p.Ile3879Phe) c.7819A>T (p.Ile2607Phe) c.7372A>T (p.Ile2458Phe) c.6709A>T (p.Ile2237Phe) c.11224A>T (p.Ile3742Phe) | COSMIC |
5 | g.13717398T>C | CA359207143 | DNAH5 | c.12622A>G (p.Ile4208Val) c.12577A>G (p.Ile4193Val) c.12730A>G (p.Ile4244Val) c.11635A>G (p.Ile3879Val) c.7819A>G (p.Ile2607Val) c.7372A>G (p.Ile2458Val) c.6709A>G (p.Ile2237Val) c.11224A>G (p.Ile3742Val) | dbSNP |
5 | g.13717398T>G | CA3201582 | DNAH5 | c.12622A>C (p.Ile4208Leu) c.12577A>C (p.Ile4193Leu) c.12730A>C (p.Ile4244Leu) c.11635A>C (p.Ile3879Leu) c.7819A>C (p.Ile2607Leu) c.7372A>C (p.Ile2458Leu) c.6709A>C (p.Ile2237Leu) c.11224A>C (p.Ile3742Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.13717398T= | CA1528407030 | DNAH5 | c.12622A= (p.Ile4208=) c.12577A= (p.Ile4193=) c.12730A= (p.Ile4244=) c.11635A= (p.Ile3879=) c.7819A= (p.Ile2607=) c.7372A= (p.Ile2458=) c.6709A= (p.Ile2237=) c.11224A= (p.Ile3742=) | |
5 | g.13717399A>C | CA359207161 | DNAH5 | c.12621T>G (p.Asn4207Lys) c.12576T>G (p.Asn4192Lys) c.12729T>G (p.Asn4243Lys) c.11634T>G (p.Asn3878Lys) c.7818T>G (p.Asn2606Lys) c.7371T>G (p.Asn2457Lys) c.6708T>G (p.Asn2236Lys) c.11223T>G (p.Asn3741Lys) | |
5 | g.13717399A>G | CA443254620 | DNAH5 | c.12621T>C (p.Asn4207=) c.12576T>C (p.Asn4192=) c.12729T>C (p.Asn4243=) c.11634T>C (p.Asn3878=) c.7818T>C (p.Asn2606=) c.7371T>C (p.Asn2457=) c.6708T>C (p.Asn2236=) c.11223T>C (p.Asn3741=) | |
5 | g.13717399A>T | CA359207163 | DNAH5 | c.12621T>A (p.Asn4207Lys) c.12576T>A (p.Asn4192Lys) c.12729T>A (p.Asn4243Lys) c.11634T>A (p.Asn3878Lys) c.7818T>A (p.Asn2606Lys) c.7371T>A (p.Asn2457Lys) c.6708T>A (p.Asn2236Lys) c.11223T>A (p.Asn3741Lys) | |
5 | g.13717400T>A | CA359207166 | DNAH5 | c.12620A>T (p.Asn4207Ile) c.12575A>T (p.Asn4192Ile) c.12728A>T (p.Asn4243Ile) c.11633A>T (p.Asn3878Ile) c.7817A>T (p.Asn2606Ile) c.7370A>T (p.Asn2457Ile) c.6707A>T (p.Asn2236Ile) c.11222A>T (p.Asn3741Ile) | |
5 | g.13717400T>C | CA359207171 | DNAH5 | c.12620A>G (p.Asn4207Ser) c.12575A>G (p.Asn4192Ser) c.12728A>G (p.Asn4243Ser) c.11633A>G (p.Asn3878Ser) c.7817A>G (p.Asn2606Ser) c.7370A>G (p.Asn2457Ser) c.6707A>G (p.Asn2236Ser) c.11222A>G (p.Asn3741Ser) | |
5 | g.13717400T>G | CA359207174 | DNAH5 | c.12620A>C (p.Asn4207Thr) c.12575A>C (p.Asn4192Thr) c.12728A>C (p.Asn4243Thr) c.11633A>C (p.Asn3878Thr) c.7817A>C (p.Asn2606Thr) c.7370A>C (p.Asn2457Thr) c.6707A>C (p.Asn2236Thr) c.11222A>C (p.Asn3741Thr) | |
5 | g.13717401T>A | CA359207178 | DNAH5 | c.12619A>T (p.Asn4207Tyr) c.12574A>T (p.Asn4192Tyr) c.12727A>T (p.Asn4243Tyr) c.11632A>T (p.Asn3878Tyr) c.7816A>T (p.Asn2606Tyr) c.7369A>T (p.Asn2457Tyr) c.6706A>T (p.Asn2236Tyr) c.11221A>T (p.Asn3741Tyr) | |
5 | g.13717401T>C | CA359207184 | DNAH5 | c.12619A>G (p.Asn4207Asp) c.12574A>G (p.Asn4192Asp) c.12727A>G (p.Asn4243Asp) c.11632A>G (p.Asn3878Asp) c.7816A>G (p.Asn2606Asp) c.7369A>G (p.Asn2457Asp) c.6706A>G (p.Asn2236Asp) c.11221A>G (p.Asn3741Asp) | |
5 | g.13717401T>G | CA359207188 | DNAH5 | c.12619A>C (p.Asn4207His) c.12574A>C (p.Asn4192His) c.12727A>C (p.Asn4243His) c.11632A>C (p.Asn3878His) c.7816A>C (p.Asn2606His) c.7369A>C (p.Asn2457His) c.6706A>C (p.Asn2236His) c.11221A>C (p.Asn3741His) | |
5 | g.13717402C>A | CA359207195 | DNAH5 | c.12618G>T (p.Trp4206Cys) c.12573G>T (p.Trp4191Cys) c.12726G>T (p.Trp4242Cys) c.11631G>T (p.Trp3877Cys) c.7815G>T (p.Trp2605Cys) c.7368G>T (p.Trp2456Cys) c.6705G>T (p.Trp2235Cys) c.11220G>T (p.Trp3740Cys) | dbSNP |
5 | g.13717402C>G | CA359207209 | DNAH5 | c.12618G>C (p.Trp4206Cys) c.12573G>C (p.Trp4191Cys) c.12726G>C (p.Trp4242Cys) c.11631G>C (p.Trp3877Cys) c.7815G>C (p.Trp2605Cys) c.7368G>C (p.Trp2456Cys) c.6705G>C (p.Trp2235Cys) c.11220G>C (p.Trp3740Cys) | |
5 | g.13717402C>T | CA359207201 | DNAH5 | c.12618G>A (p.Trp4206Ter) c.12573G>A (p.Trp4191Ter) c.12726G>A (p.Trp4242Ter) c.11631G>A (p.Trp3877Ter) c.7815G>A (p.Trp2605Ter) c.7368G>A (p.Trp2456Ter) c.6705G>A (p.Trp2235Ter) c.11220G>A (p.Trp3740Ter) | |
5 | g.13717403C>A | CA359207211 | DNAH5 | c.12617G>T (p.Trp4206Leu) c.12572G>T (p.Trp4191Leu) c.12725G>T (p.Trp4242Leu) c.11630G>T (p.Trp3877Leu) c.7814G>T (p.Trp2605Leu) c.7367G>T (p.Trp2456Leu) c.6704G>T (p.Trp2235Leu) c.11219G>T (p.Trp3740Leu) | COSMIC |
5 | g.13717403C= | CA1528407031 | DNAH5 | c.12617G= (p.Trp4206=) c.12572G= (p.Trp4191=) c.12725G= (p.Trp4242=) c.11630G= (p.Trp3877=) c.7814G= (p.Trp2605=) c.7367G= (p.Trp2456=) c.6704G= (p.Trp2235=) c.11219G= (p.Trp3740=) | |
5 | g.13717403C>G | CA359207213 | DNAH5 | c.12617G>C (p.Trp4206Ser) c.12572G>C (p.Trp4191Ser) c.12725G>C (p.Trp4242Ser) c.11630G>C (p.Trp3877Ser) c.7814G>C (p.Trp2605Ser) c.7367G>C (p.Trp2456Ser) c.6704G>C (p.Trp2235Ser) c.11219G>C (p.Trp3740Ser) | |
5 | g.13717403C>T | CA3201583 | DNAH5 | c.12617G>A (p.Trp4206Ter) c.12572G>A (p.Trp4191Ter) c.12725G>A (p.Trp4242Ter) c.11630G>A (p.Trp3877Ter) c.7814G>A (p.Trp2605Ter) c.7367G>A (p.Trp2456Ter) c.6704G>A (p.Trp2235Ter) c.11219G>A (p.Trp3740Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
5 | g.13717404A>C | CA359207225 | DNAH5 | c.12616T>G (p.Trp4206Gly) c.12571T>G (p.Trp4191Gly) c.12724T>G (p.Trp4242Gly) c.11629T>G (p.Trp3877Gly) c.7813T>G (p.Trp2605Gly) c.7366T>G (p.Trp2456Gly) c.6703T>G (p.Trp2235Gly) c.11218T>G (p.Trp3740Gly) | |
5 | g.13717404A>G | CA359207228 | DNAH5 | c.12616T>C (p.Trp4206Arg) c.12571T>C (p.Trp4191Arg) c.12724T>C (p.Trp4242Arg) c.11629T>C (p.Trp3877Arg) c.7813T>C (p.Trp2605Arg) c.7366T>C (p.Trp2456Arg) c.6703T>C (p.Trp2235Arg) c.11218T>C (p.Trp3740Arg) | |
5 | g.13717404A>T | CA359207233 | DNAH5 | c.12616T>A (p.Trp4206Arg) c.12571T>A (p.Trp4191Arg) c.12724T>A (p.Trp4242Arg) c.11629T>A (p.Trp3877Arg) c.7813T>A (p.Trp2605Arg) c.7366T>A (p.Trp2456Arg) c.6703T>A (p.Trp2235Arg) c.11218T>A (p.Trp3740Arg) | |
5 | g.13717405C>A | CA443254634 | DNAH5 | c.12615G>T (p.Gly4205=) c.12570G>T (p.Gly4190=) c.12723G>T (p.Gly4241=) c.11628G>T (p.Gly3876=) c.7812G>T (p.Gly2604=) c.7365G>T (p.Gly2455=) c.6702G>T (p.Gly2234=) c.11217G>T (p.Gly3739=) | ClinVar dbSNP gnomAD v4 |
5 | g.13717405C= | CA1528407032 | DNAH5 | c.12615G= (p.Gly4205=) c.12570G= (p.Gly4190=) c.12723G= (p.Gly4241=) c.11628G= (p.Gly3876=) c.7812G= (p.Gly2604=) c.7365G= (p.Gly2455=) c.6702G= (p.Gly2234=) c.11217G= (p.Gly3739=) | |
5 | g.13717405C>G | CA443254637 | DNAH5 | c.12615G>C (p.Gly4205=) c.12570G>C (p.Gly4190=) c.12723G>C (p.Gly4241=) c.11628G>C (p.Gly3876=) c.7812G>C (p.Gly2604=) c.7365G>C (p.Gly2455=) c.6702G>C (p.Gly2234=) c.11217G>C (p.Gly3739=) | |
5 | g.13717405C>T | CA3201584 | DNAH5 | c.12615G>A (p.Gly4205=) c.12570G>A (p.Gly4190=) c.12723G>A (p.Gly4241=) c.11628G>A (p.Gly3876=) c.7812G>A (p.Gly2604=) c.7365G>A (p.Gly2455=) c.6702G>A (p.Gly2234=) c.11217G>A (p.Gly3739=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.13717406C>A | CA113919224 | DNAH5 | c.12614G>T (p.Gly4205Val) c.12569G>T (p.Gly4190Val) c.12722G>T (p.Gly4241Val) c.11627G>T (p.Gly3876Val) c.7811G>T (p.Gly2604Val) c.7364G>T (p.Gly2455Val) c.6701G>T (p.Gly2234Val) c.11216G>T (p.Gly3739Val) | ClinVar dbSNP |
5 | g.13717406C= | CA1528407033 | DNAH5 | c.12614G= (p.Gly4205=) c.12569G= (p.Gly4190=) c.12722G= (p.Gly4241=) c.11627G= (p.Gly3876=) c.7811G= (p.Gly2604=) c.7364G= (p.Gly2455=) c.6701G= (p.Gly2234=) c.11216G= (p.Gly3739=) | |
5 | g.13717406C>G | CA359207250 | DNAH5 | c.12614G>C (p.Gly4205Ala) c.12569G>C (p.Gly4190Ala) c.12722G>C (p.Gly4241Ala) c.11627G>C (p.Gly3876Ala) c.7811G>C (p.Gly2604Ala) c.7364G>C (p.Gly2455Ala) c.6701G>C (p.Gly2234Ala) c.11216G>C (p.Gly3739Ala) | |
5 | g.13717406C>T | CA359207255 | DNAH5 | c.12614G>A (p.Gly4205Glu) c.12569G>A (p.Gly4190Glu) c.12722G>A (p.Gly4241Glu) c.11627G>A (p.Gly3876Glu) c.7811G>A (p.Gly2604Glu) c.7364G>A (p.Gly2455Glu) c.6701G>A (p.Gly2234Glu) c.11216G>A (p.Gly3739Glu) | |
5 | g.13717407C>A | CA359207276 | DNAH5 | c.12613G>T (p.Gly4205Trp) c.12568G>T (p.Gly4190Trp) c.12721G>T (p.Gly4241Trp) c.11626G>T (p.Gly3876Trp) c.7810G>T (p.Gly2604Trp) c.7363G>T (p.Gly2455Trp) c.6700G>T (p.Gly2234Trp) c.11215G>T (p.Gly3739Trp) | |
5 | g.13717407C>G | CA359207277 | DNAH5 | c.12613G>C (p.Gly4205Arg) c.12568G>C (p.Gly4190Arg) c.12721G>C (p.Gly4241Arg) c.11626G>C (p.Gly3876Arg) c.7810G>C (p.Gly2604Arg) c.7363G>C (p.Gly2455Arg) c.6700G>C (p.Gly2234Arg) c.11215G>C (p.Gly3739Arg) | |
5 | g.13717407C>T | CA359207260 | DNAH5 | c.12613G>A (p.Gly4205Arg) c.12568G>A (p.Gly4190Arg) c.12721G>A (p.Gly4241Arg) c.11626G>A (p.Gly3876Arg) c.7810G>A (p.Gly2604Arg) c.7363G>A (p.Gly2455Arg) c.6700G>A (p.Gly2234Arg) c.11215G>A (p.Gly3739Arg) | |
5 | g.13717408C>A | CA443254645 | DNAH5 | c.12612G>T (p.Leu4204=) c.12567G>T (p.Leu4189=) c.12720G>T (p.Leu4240=) c.11625G>T (p.Leu3875=) c.7809G>T (p.Leu2603=) c.7362G>T (p.Leu2454=) c.6699G>T (p.Leu2233=) c.11214G>T (p.Leu3738=) | |
5 | g.13717408C>G | CA443254647 | DNAH5 | c.12612G>C (p.Leu4204=) c.12567G>C (p.Leu4189=) c.12720G>C (p.Leu4240=) c.11625G>C (p.Leu3875=) c.7809G>C (p.Leu2603=) c.7362G>C (p.Leu2454=) c.6699G>C (p.Leu2233=) c.11214G>C (p.Leu3738=) | |
5 | g.13717408C>T | CA443254651 | DNAH5 | c.12612G>A (p.Leu4204=) c.12567G>A (p.Leu4189=) c.12720G>A (p.Leu4240=) c.11625G>A (p.Leu3875=) c.7809G>A (p.Leu2603=) c.7362G>A (p.Leu2454=) c.6699G>A (p.Leu2233=) c.11214G>A (p.Leu3738=) | |
5 | g.13717409A>C | CA359207280 | DNAH5 | c.12611T>G (p.Leu4204Arg) c.12566T>G (p.Leu4189Arg) c.12719T>G (p.Leu4240Arg) c.11624T>G (p.Leu3875Arg) c.7808T>G (p.Leu2603Arg) c.7361T>G (p.Leu2454Arg) c.6698T>G (p.Leu2233Arg) c.11213T>G (p.Leu3738Arg) | |
5 | g.13717409A>G | CA359207281 | DNAH5 | c.12611T>C (p.Leu4204Pro) c.12566T>C (p.Leu4189Pro) c.12719T>C (p.Leu4240Pro) c.11624T>C (p.Leu3875Pro) c.7808T>C (p.Leu2603Pro) c.7361T>C (p.Leu2454Pro) c.6698T>C (p.Leu2233Pro) c.11213T>C (p.Leu3738Pro) | |
5 | g.13717409A>T | CA359207288 | DNAH5 | c.12611T>A (p.Leu4204Gln) c.12566T>A (p.Leu4189Gln) c.12719T>A (p.Leu4240Gln) c.11624T>A (p.Leu3875Gln) c.7808T>A (p.Leu2603Gln) c.7361T>A (p.Leu2454Gln) c.6698T>A (p.Leu2233Gln) c.11213T>A (p.Leu3738Gln) | |
5 | g.13717410G>A | CA443254657 | DNAH5 | c.12610C>T (p.Leu4204=) c.12565C>T (p.Leu4189=) c.12718C>T (p.Leu4240=) c.11623C>T (p.Leu3875=) c.7807C>T (p.Leu2603=) c.7360C>T (p.Leu2454=) c.6697C>T (p.Leu2233=) c.11212C>T (p.Leu3738=) | |
5 | g.13717410G>C | CA359207292 | DNAH5 | c.12610C>G (p.Leu4204Val) c.12565C>G (p.Leu4189Val) c.12718C>G (p.Leu4240Val) c.11623C>G (p.Leu3875Val) c.7807C>G (p.Leu2603Val) c.7360C>G (p.Leu2454Val) c.6697C>G (p.Leu2233Val) c.11212C>G (p.Leu3738Val) | |
5 | g.13717410G>T | CA359207303 | DNAH5 | c.12610C>A (p.Leu4204Met) c.12565C>A (p.Leu4189Met) c.12718C>A (p.Leu4240Met) c.11623C>A (p.Leu3875Met) c.7807C>A (p.Leu2603Met) c.7360C>A (p.Leu2454Met) c.6697C>A (p.Leu2233Met) c.11212C>A (p.Leu3738Met) | COSMIC |
5 | g.13717411G>A | CA443254663 | DNAH5 | c.12609C>T (p.Ala4203=) c.12564C>T (p.Ala4188=) c.12717C>T (p.Ala4239=) c.11622C>T (p.Ala3874=) c.7806C>T (p.Ala2602=) c.7359C>T (p.Ala2453=) c.6696C>T (p.Ala2232=) c.11211C>T (p.Ala3737=) | |
5 | g.13717411G>C | CA443254669 | DNAH5 | c.12609C>G (p.Ala4203=) c.12564C>G (p.Ala4188=) c.12717C>G (p.Ala4239=) c.11622C>G (p.Ala3874=) c.7806C>G (p.Ala2602=) c.7359C>G (p.Ala2453=) c.6696C>G (p.Ala2232=) c.11211C>G (p.Ala3737=) | |
5 | g.13717411G>T | CA443254665 | DNAH5 | c.12609C>A (p.Ala4203=) c.12564C>A (p.Ala4188=) c.12717C>A (p.Ala4239=) c.11622C>A (p.Ala3874=) c.7806C>A (p.Ala2602=) c.7359C>A (p.Ala2453=) c.6696C>A (p.Ala2232=) c.11211C>A (p.Ala3737=) | |
5 | g.13717412G>A | CA3201585 | DNAH5 | c.12608C>T (p.Ala4203Val) c.12563C>T (p.Ala4188Val) c.12716C>T (p.Ala4239Val) c.11621C>T (p.Ala3874Val) c.7805C>T (p.Ala2602Val) c.7358C>T (p.Ala2453Val) c.6695C>T (p.Ala2232Val) c.11210C>T (p.Ala3737Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |