Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.13717397A>CCA359207112DNAH5c.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
5g.13717397A>GCA359207085DNAH5c.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)
5g.13717397A>TCA359207091DNAH5c.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)
5g.13717398T>ACA359207127DNAH5c.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
5g.13717398T>CCA359207143DNAH5c.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
5g.13717398T>GCA3201582DNAH5c.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
5g.13717398T=CA1528407030DNAH5c.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=)
5g.13717399A>CCA359207161DNAH5c.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)
5g.13717399A>GCA443254620DNAH5c.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=)
5g.13717399A>TCA359207163DNAH5c.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)
5g.13717400T>ACA359207166DNAH5c.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)
5g.13717400T>CCA359207171DNAH5c.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)
5g.13717400T>GCA359207174DNAH5c.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)
5g.13717401T>ACA359207178DNAH5c.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)
5g.13717401T>CCA359207184DNAH5c.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)
5g.13717401T>GCA359207188DNAH5c.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)
5g.13717402C>ACA359207195DNAH5c.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
5g.13717402C>GCA359207209DNAH5c.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)
5g.13717402C>TCA359207201DNAH5c.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)
5g.13717403C>ACA359207211DNAH5c.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
5g.13717403C=CA1528407031DNAH5c.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=)
5g.13717403C>GCA359207213DNAH5c.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)
5g.13717403C>TCA3201583DNAH5c.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
5g.13717404A>CCA359207225DNAH5c.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)
5g.13717404A>GCA359207228DNAH5c.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)
5g.13717404A>TCA359207233DNAH5c.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)
5g.13717405C>ACA443254634DNAH5c.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
5g.13717405C=CA1528407032DNAH5c.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=)
5g.13717405C>GCA443254637DNAH5c.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=)
5g.13717405C>TCA3201584DNAH5c.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
5g.13717406C>ACA113919224DNAH5c.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
5g.13717406C=CA1528407033DNAH5c.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=)
5g.13717406C>GCA359207250DNAH5c.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)
5g.13717406C>TCA359207255DNAH5c.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)
5g.13717407C>ACA359207276DNAH5c.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)
5g.13717407C>GCA359207277DNAH5c.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)
5g.13717407C>TCA359207260DNAH5c.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)
5g.13717408C>ACA443254645DNAH5c.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=)
5g.13717408C>GCA443254647DNAH5c.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=)
5g.13717408C>TCA443254651DNAH5c.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=)
5g.13717409A>CCA359207280DNAH5c.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)
5g.13717409A>GCA359207281DNAH5c.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)
5g.13717409A>TCA359207288DNAH5c.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)
5g.13717410G>ACA443254657DNAH5c.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=)
5g.13717410G>CCA359207292DNAH5c.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)
5g.13717410G>TCA359207303DNAH5c.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
5g.13717411G>ACA443254663DNAH5c.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=)
5g.13717411G>CCA443254669DNAH5c.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=)
5g.13717411G>TCA443254665DNAH5c.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=)
5g.13717412G>ACA3201585DNAH5c.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

Number of alleles fetched