Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.178740380C>ACA349610139TTNc.10361-2020G>T (n.10361-2020G>T)
c.12340G>T (p.Val4114Leu)
c.12139G>T (p.Val4047Leu)
c.11764G>T (p.Val3922Leu)
c.12853G>T (p.Val4285Leu)
c.11902G>T (p.Val3968Leu)
c.11950G>T (p.Val3984Leu)
c.11809G>T (p.Val3937Leu)
c.11905G>T (p.Val3969Leu)
c.10364-2020G>T (n.10364-2020G>T)
2g.178740380C>GCA349610135TTNc.10361-2020G>C (n.10361-2020G>C)
c.12340G>C (p.Val4114Leu)
c.12139G>C (p.Val4047Leu)
c.11764G>C (p.Val3922Leu)
c.12853G>C (p.Val4285Leu)
c.11902G>C (p.Val3968Leu)
c.11950G>C (p.Val3984Leu)
c.11809G>C (p.Val3937Leu)
c.11905G>C (p.Val3969Leu)
c.10364-2020G>C (n.10364-2020G>C)
2g.178740380C>TCA349610137TTNc.10361-2020G>A (n.10361-2020G>A)
c.12340G>A (p.Val4114Ile)
c.12139G>A (p.Val4047Ile)
c.11764G>A (p.Val3922Ile)
c.12853G>A (p.Val4285Ile)
c.11902G>A (p.Val3968Ile)
c.11950G>A (p.Val3984Ile)
c.11809G>A (p.Val3937Ile)
c.11905G>A (p.Val3969Ile)
c.10364-2020G>A (n.10364-2020G>A)
gnomAD v4
2g.178740381C>ACA349610141TTNc.10361-2021G>T (n.10361-2021G>T)
c.12339G>T (p.Gln4113His)
c.12138G>T (p.Gln4046His)
c.11763G>T (p.Gln3921His)
c.12852G>T (p.Gln4284His)
c.11901G>T (p.Gln3967His)
c.11949G>T (p.Gln3983His)
c.11808G>T (p.Gln3936His)
c.11904G>T (p.Gln3968His)
c.10364-2021G>T (n.10364-2021G>T)
2g.178740381C>GCA349610142TTNc.10361-2021G>C (n.10361-2021G>C)
c.12339G>C (p.Gln4113His)
c.12138G>C (p.Gln4046His)
c.11763G>C (p.Gln3921His)
c.12852G>C (p.Gln4284His)
c.11901G>C (p.Gln3967His)
c.11949G>C (p.Gln3983His)
c.11808G>C (p.Gln3936His)
c.11904G>C (p.Gln3968His)
c.10364-2021G>C (n.10364-2021G>C)
gnomAD v4
2g.178740381C>TCA430295954TTNc.10361-2021G>A (n.10361-2021G>A)
c.12339G>A (p.Gln4113=)
c.12138G>A (p.Gln4046=)
c.11763G>A (p.Gln3921=)
c.12852G>A (p.Gln4284=)
c.11901G>A (p.Gln3967=)
c.11949G>A (p.Gln3983=)
c.11808G>A (p.Gln3936=)
c.11904G>A (p.Gln3968=)
c.10364-2021G>A (n.10364-2021G>A)
COSMIC COSMIC
2g.178740382T>ACA349610145TTNc.10361-2022A>T (n.10361-2022A>T)
c.12338A>T (p.Gln4113Leu)
c.12137A>T (p.Gln4046Leu)
c.11762A>T (p.Gln3921Leu)
c.12851A>T (p.Gln4284Leu)
c.11900A>T (p.Gln3967Leu)
c.11948A>T (p.Gln3983Leu)
c.11807A>T (p.Gln3936Leu)
c.11903A>T (p.Gln3968Leu)
c.10364-2022A>T (n.10364-2022A>T)
2g.178740382T>CCA349610146TTNc.10361-2022A>G (n.10361-2022A>G)
c.12338A>G (p.Gln4113Arg)
c.12137A>G (p.Gln4046Arg)
c.11762A>G (p.Gln3921Arg)
c.12851A>G (p.Gln4284Arg)
c.11900A>G (p.Gln3967Arg)
c.11948A>G (p.Gln3983Arg)
c.11807A>G (p.Gln3936Arg)
c.11903A>G (p.Gln3968Arg)
c.10364-2022A>G (n.10364-2022A>G)
2g.178740382T>GCA10576560TTNc.10361-2022A>C (n.10361-2022A>C)
c.12338A>C (p.Gln4113Pro)
c.12137A>C (p.Gln4046Pro)
c.11762A>C (p.Gln3921Pro)
c.12851A>C (p.Gln4284Pro)
c.11900A>C (p.Gln3967Pro)
c.11948A>C (p.Gln3983Pro)
c.11807A>C (p.Gln3936Pro)
c.11903A>C (p.Gln3968Pro)
c.10364-2022A>C (n.10364-2022A>C)
ClinVar dbSNP gnomAD v4
2g.178740382T=CA1310601312TTNc.10361-2022A= (n.10361-2022A=)
c.12338A= (p.Gln4113=)
c.12137A= (p.Gln4046=)
c.11762A= (p.Gln3921=)
c.12851A= (p.Gln4284=)
c.11900A= (p.Gln3967=)
c.11948A= (p.Gln3983=)
c.11807A= (p.Gln3936=)
c.11903A= (p.Gln3968=)
c.10364-2022A= (n.10364-2022A=)
2g.178740383G>ACA349610150TTNc.10361-2023C>T (n.10361-2023C>T)
c.12337C>T (p.Gln4113Ter)
c.12136C>T (p.Gln4046Ter)
c.11761C>T (p.Gln3921Ter)
c.12850C>T (p.Gln4284Ter)
c.11899C>T (p.Gln3967Ter)
c.11947C>T (p.Gln3983Ter)
c.11806C>T (p.Gln3936Ter)
c.11902C>T (p.Gln3968Ter)
c.10364-2023C>T (n.10364-2023C>T)
ClinVar dbSNP
2g.178740383G>CCA349610151TTNc.10361-2023C>G (n.10361-2023C>G)
c.12337C>G (p.Gln4113Glu)
c.12136C>G (p.Gln4046Glu)
c.11761C>G (p.Gln3921Glu)
c.12850C>G (p.Gln4284Glu)
c.11899C>G (p.Gln3967Glu)
c.11947C>G (p.Gln3983Glu)
c.11806C>G (p.Gln3936Glu)
c.11902C>G (p.Gln3968Glu)
c.10364-2023C>G (n.10364-2023C>G)
2g.178740383G=CA1310601314TTNc.10361-2023C= (n.10361-2023C=)
c.12337C= (p.Gln4113=)
c.12136C= (p.Gln4046=)
c.11761C= (p.Gln3921=)
c.12850C= (p.Gln4284=)
c.11899C= (p.Gln3967=)
c.11947C= (p.Gln3983=)
c.11806C= (p.Gln3936=)
c.11902C= (p.Gln3968=)
c.10364-2023C= (n.10364-2023C=)
2g.178740383G>TCA349610153TTNc.10361-2023C>A (n.10361-2023C>A)
c.12337C>A (p.Gln4113Lys)
c.12136C>A (p.Gln4046Lys)
c.11761C>A (p.Gln3921Lys)
c.12850C>A (p.Gln4284Lys)
c.11899C>A (p.Gln3967Lys)
c.11947C>A (p.Gln3983Lys)
c.11806C>A (p.Gln3936Lys)
c.11902C>A (p.Gln3968Lys)
c.10364-2023C>A (n.10364-2023C>A)
2g.178740384A=CA1310601316TTNc.10361-2024T= (n.10361-2024T=)
c.12336T= (p.Ser4112=)
c.12135T= (p.Ser4045=)
c.11760T= (p.Ser3920=)
c.12849T= (p.Ser4283=)
c.11898T= (p.Ser3966=)
c.11946T= (p.Ser3982=)
c.11805T= (p.Ser3935=)
c.11901T= (p.Ser3967=)
c.10364-2024T= (n.10364-2024T=)
2g.178740384A>CCA430295960TTNc.10361-2024T>G (n.10361-2024T>G)
c.12336T>G (p.Ser4112=)
c.12135T>G (p.Ser4045=)
c.11760T>G (p.Ser3920=)
c.12849T>G (p.Ser4283=)
c.11898T>G (p.Ser3966=)
c.11946T>G (p.Ser3982=)
c.11805T>G (p.Ser3935=)
c.11901T>G (p.Ser3967=)
c.10364-2024T>G (n.10364-2024T>G)
2g.178740384A>GCA430295962TTNc.10361-2024T>C (n.10361-2024T>C)
c.12336T>C (p.Ser4112=)
c.12135T>C (p.Ser4045=)
c.11760T>C (p.Ser3920=)
c.12849T>C (p.Ser4283=)
c.11898T>C (p.Ser3966=)
c.11946T>C (p.Ser3982=)
c.11805T>C (p.Ser3935=)
c.11901T>C (p.Ser3967=)
c.10364-2024T>C (n.10364-2024T>C)
dbSNP gnomAD v2 gnomAD v4
2g.178740384A>TCA430295961TTNc.10361-2024T>A (n.10361-2024T>A)
c.12336T>A (p.Ser4112=)
c.12135T>A (p.Ser4045=)
c.11760T>A (p.Ser3920=)
c.12849T>A (p.Ser4283=)
c.11898T>A (p.Ser3966=)
c.11946T>A (p.Ser3982=)
c.11805T>A (p.Ser3935=)
c.11901T>A (p.Ser3967=)
c.10364-2024T>A (n.10364-2024T>A)
2g.178740385G>ACA349610156TTNc.10361-2025C>T (n.10361-2025C>T)
c.12335C>T (p.Ser4112Phe)
c.12134C>T (p.Ser4045Phe)
c.11759C>T (p.Ser3920Phe)
c.12848C>T (p.Ser4283Phe)
c.11897C>T (p.Ser3966Phe)
c.11945C>T (p.Ser3982Phe)
c.11804C>T (p.Ser3935Phe)
c.11900C>T (p.Ser3967Phe)
c.10364-2025C>T (n.10364-2025C>T)
2g.178740385G>CCA349610157TTNc.10361-2025C>G (n.10361-2025C>G)
c.12335C>G (p.Ser4112Cys)
c.12134C>G (p.Ser4045Cys)
c.11759C>G (p.Ser3920Cys)
c.12848C>G (p.Ser4283Cys)
c.11897C>G (p.Ser3966Cys)
c.11945C>G (p.Ser3982Cys)
c.11804C>G (p.Ser3935Cys)
c.11900C>G (p.Ser3967Cys)
c.10364-2025C>G (n.10364-2025C>G)
2g.178740385G>TCA349610158TTNc.10361-2025C>A (n.10361-2025C>A)
c.12335C>A (p.Ser4112Tyr)
c.12134C>A (p.Ser4045Tyr)
c.11759C>A (p.Ser3920Tyr)
c.12848C>A (p.Ser4283Tyr)
c.11897C>A (p.Ser3966Tyr)
c.11945C>A (p.Ser3982Tyr)
c.11804C>A (p.Ser3935Tyr)
c.11900C>A (p.Ser3967Tyr)
c.10364-2025C>A (n.10364-2025C>A)
COSMIC COSMIC
2g.178740385dupCA2662152725TTNc.10361-2025dup (n.10361-2025dup)
c.12335dup (p.Gln4113SerfsTer5)
c.12134dup (p.Gln4046SerfsTer5)
c.11759dup (p.Gln3921SerfsTer5)
c.12848dup (p.Gln4284SerfsTer5)
c.11897dup (p.Gln3967SerfsTer5)
c.11945dup (p.Gln3983SerfsTer5)
c.11804dup (p.Gln3936SerfsTer5)
c.11900dup (p.Gln3968SerfsTer5)
c.10364-2025dup (n.10364-2025dup)
gnomAD v4
2g.178740386A>CCA349610165TTNc.10361-2026T>G (n.10361-2026T>G)
c.12334T>G (p.Ser4112Ala)
c.12133T>G (p.Ser4045Ala)
c.11758T>G (p.Ser3920Ala)
c.12847T>G (p.Ser4283Ala)
c.11896T>G (p.Ser3966Ala)
c.11944T>G (p.Ser3982Ala)
c.11803T>G (p.Ser3935Ala)
c.11899T>G (p.Ser3967Ala)
c.10364-2026T>G (n.10364-2026T>G)
2g.178740386A>GCA349610163TTNc.10361-2026T>C (n.10361-2026T>C)
c.12334T>C (p.Ser4112Pro)
c.12133T>C (p.Ser4045Pro)
c.11758T>C (p.Ser3920Pro)
c.12847T>C (p.Ser4283Pro)
c.11896T>C (p.Ser3966Pro)
c.11944T>C (p.Ser3982Pro)
c.11803T>C (p.Ser3935Pro)
c.11899T>C (p.Ser3967Pro)
c.10364-2026T>C (n.10364-2026T>C)
2g.178740386A>TCA349610162TTNc.10361-2026T>A (n.10361-2026T>A)
c.12334T>A (p.Ser4112Thr)
c.12133T>A (p.Ser4045Thr)
c.11758T>A (p.Ser3920Thr)
c.12847T>A (p.Ser4283Thr)
c.11896T>A (p.Ser3966Thr)
c.11944T>A (p.Ser3982Thr)
c.11803T>A (p.Ser3935Thr)
c.11899T>A (p.Ser3967Thr)
c.10364-2026T>A (n.10364-2026T>A)
2g.178740387G>ACA430295966TTNc.10361-2027C>T (n.10361-2027C>T)
c.12333C>T (p.Ile4111=)
c.12132C>T (p.Ile4044=)
c.11757C>T (p.Ile3919=)
c.12846C>T (p.Ile4282=)
c.11895C>T (p.Ile3965=)
c.11943C>T (p.Ile3981=)
c.11802C>T (p.Ile3934=)
c.11898C>T (p.Ile3966=)
c.10364-2027C>T (n.10364-2027C>T)
2g.178740387G>CCA349610167TTNc.10361-2027C>G (n.10361-2027C>G)
c.12333C>G (p.Ile4111Met)
c.12132C>G (p.Ile4044Met)
c.11757C>G (p.Ile3919Met)
c.12846C>G (p.Ile4282Met)
c.11895C>G (p.Ile3965Met)
c.11943C>G (p.Ile3981Met)
c.11802C>G (p.Ile3934Met)
c.11898C>G (p.Ile3966Met)
c.10364-2027C>G (n.10364-2027C>G)
2g.178740387G>TCA430295968TTNc.10361-2027C>A (n.10361-2027C>A)
c.12333C>A (p.Ile4111=)
c.12132C>A (p.Ile4044=)
c.11757C>A (p.Ile3919=)
c.12846C>A (p.Ile4282=)
c.11895C>A (p.Ile3965=)
c.11943C>A (p.Ile3981=)
c.11802C>A (p.Ile3934=)
c.11898C>A (p.Ile3966=)
c.10364-2027C>A (n.10364-2027C>A)
2g.178740388A=CA1310601317TTNc.10361-2028T= (n.10361-2028T=)
c.12332T= (p.Ile4111=)
c.12131T= (p.Ile4044=)
c.11756T= (p.Ile3919=)
c.12845T= (p.Ile4282=)
c.11894T= (p.Ile3965=)
c.11942T= (p.Ile3981=)
c.11801T= (p.Ile3934=)
c.11897T= (p.Ile3966=)
c.10364-2028T= (n.10364-2028T=)
2g.178740388A>CCA349610170TTNc.10361-2028T>G (n.10361-2028T>G)
c.12332T>G (p.Ile4111Ser)
c.12131T>G (p.Ile4044Ser)
c.11756T>G (p.Ile3919Ser)
c.12845T>G (p.Ile4282Ser)
c.11894T>G (p.Ile3965Ser)
c.11942T>G (p.Ile3981Ser)
c.11801T>G (p.Ile3934Ser)
c.11897T>G (p.Ile3966Ser)
c.10364-2028T>G (n.10364-2028T>G)
2g.178740388A>GCA349610172TTNc.10361-2028T>C (n.10361-2028T>C)
c.12332T>C (p.Ile4111Thr)
c.12131T>C (p.Ile4044Thr)
c.11756T>C (p.Ile3919Thr)
c.12845T>C (p.Ile4282Thr)
c.11894T>C (p.Ile3965Thr)
c.11942T>C (p.Ile3981Thr)
c.11801T>C (p.Ile3934Thr)
c.11897T>C (p.Ile3966Thr)
c.10364-2028T>C (n.10364-2028T>C)
dbSNP gnomAD v4
2g.178740388A>TCA2002659TTNc.10361-2028T>A (n.10361-2028T>A)
c.12332T>A (p.Ile4111Asn)
c.12131T>A (p.Ile4044Asn)
c.11756T>A (p.Ile3919Asn)
c.12845T>A (p.Ile4282Asn)
c.11894T>A (p.Ile3965Asn)
c.11942T>A (p.Ile3981Asn)
c.11801T>A (p.Ile3934Asn)
c.11897T>A (p.Ile3966Asn)
c.10364-2028T>A (n.10364-2028T>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.178740389T>ACA349610175TTNc.10361-2029A>T (n.10361-2029A>T)
c.12331A>T (p.Ile4111Phe)
c.12130A>T (p.Ile4044Phe)
c.11755A>T (p.Ile3919Phe)
c.12844A>T (p.Ile4282Phe)
c.11893A>T (p.Ile3965Phe)
c.11941A>T (p.Ile3981Phe)
c.11800A>T (p.Ile3934Phe)
c.11896A>T (p.Ile3966Phe)
c.10364-2029A>T (n.10364-2029A>T)
2g.178740389T>CCA349610177TTNc.10361-2029A>G (n.10361-2029A>G)
c.12331A>G (p.Ile4111Val)
c.12130A>G (p.Ile4044Val)
c.11755A>G (p.Ile3919Val)
c.12844A>G (p.Ile4282Val)
c.11893A>G (p.Ile3965Val)
c.11941A>G (p.Ile3981Val)
c.11800A>G (p.Ile3934Val)
c.11896A>G (p.Ile3966Val)
c.10364-2029A>G (n.10364-2029A>G)
2g.178740389T>GCA2002660TTNc.10361-2029A>C (n.10361-2029A>C)
c.12331A>C (p.Ile4111Leu)
c.12130A>C (p.Ile4044Leu)
c.11755A>C (p.Ile3919Leu)
c.12844A>C (p.Ile4282Leu)
c.11893A>C (p.Ile3965Leu)
c.11941A>C (p.Ile3981Leu)
c.11800A>C (p.Ile3934Leu)
c.11896A>C (p.Ile3966Leu)
c.10364-2029A>C (n.10364-2029A>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.178740389T=CA1310601320TTNc.10361-2029A= (n.10361-2029A=)
c.12331A= (p.Ile4111=)
c.12130A= (p.Ile4044=)
c.11755A= (p.Ile3919=)
c.12844A= (p.Ile4282=)
c.11893A= (p.Ile3965=)
c.11941A= (p.Ile3981=)
c.11800A= (p.Ile3934=)
c.11896A= (p.Ile3966=)
c.10364-2029A= (n.10364-2029A=)
2g.178740390C>ACA2002661TTNc.10361-2030G>T (n.10361-2030G>T)
c.12330G>T (p.Met4110Ile)
c.12129G>T (p.Met4043Ile)
c.11754G>T (p.Met3918Ile)
c.12843G>T (p.Met4281Ile)
c.11892G>T (p.Met3964Ile)
c.11940G>T (p.Met3980Ile)
c.11799G>T (p.Met3933Ile)
c.11895G>T (p.Met3965Ile)
c.10364-2030G>T (n.10364-2030G>T)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.178740390C=CA1310601322TTNc.10361-2030G= (n.10361-2030G=)
c.12330G= (p.Met4110=)
c.12129G= (p.Met4043=)
c.11754G= (p.Met3918=)
c.12843G= (p.Met4281=)
c.11892G= (p.Met3964=)
c.11940G= (p.Met3980=)
c.11799G= (p.Met3933=)
c.11895G= (p.Met3965=)
c.10364-2030G= (n.10364-2030G=)
2g.178740390C>GCA349610181TTNc.10361-2030G>C (n.10361-2030G>C)
c.12330G>C (p.Met4110Ile)
c.12129G>C (p.Met4043Ile)
c.11754G>C (p.Met3918Ile)
c.12843G>C (p.Met4281Ile)
c.11892G>C (p.Met3964Ile)
c.11940G>C (p.Met3980Ile)
c.11799G>C (p.Met3933Ile)
c.11895G>C (p.Met3965Ile)
c.10364-2030G>C (n.10364-2030G>C)
2g.178740390C>TCA349610183TTNc.10361-2030G>A (n.10361-2030G>A)
c.12330G>A (p.Met4110Ile)
c.12129G>A (p.Met4043Ile)
c.11754G>A (p.Met3918Ile)
c.12843G>A (p.Met4281Ile)
c.11892G>A (p.Met3964Ile)
c.11940G>A (p.Met3980Ile)
c.11799G>A (p.Met3933Ile)
c.11895G>A (p.Met3965Ile)
c.10364-2030G>A (n.10364-2030G>A)
2g.178740391A>CCA349610185TTNc.10361-2031T>G (n.10361-2031T>G)
c.12329T>G (p.Met4110Arg)
c.12128T>G (p.Met4043Arg)
c.11753T>G (p.Met3918Arg)
c.12842T>G (p.Met4281Arg)
c.11891T>G (p.Met3964Arg)
c.11939T>G (p.Met3980Arg)
c.11798T>G (p.Met3933Arg)
c.11894T>G (p.Met3965Arg)
c.10364-2031T>G (n.10364-2031T>G)
2g.178740391A>GCA349610186TTNc.10361-2031T>C (n.10361-2031T>C)
c.12329T>C (p.Met4110Thr)
c.12128T>C (p.Met4043Thr)
c.11753T>C (p.Met3918Thr)
c.12842T>C (p.Met4281Thr)
c.11891T>C (p.Met3964Thr)
c.11939T>C (p.Met3980Thr)
c.11798T>C (p.Met3933Thr)
c.11894T>C (p.Met3965Thr)
c.10364-2031T>C (n.10364-2031T>C)
2g.178740391A>TCA349610187TTNc.10361-2031T>A (n.10361-2031T>A)
c.12329T>A (p.Met4110Lys)
c.12128T>A (p.Met4043Lys)
c.11753T>A (p.Met3918Lys)
c.12842T>A (p.Met4281Lys)
c.11891T>A (p.Met3964Lys)
c.11939T>A (p.Met3980Lys)
c.11798T>A (p.Met3933Lys)
c.11894T>A (p.Met3965Lys)
c.10364-2031T>A (n.10364-2031T>A)
2g.178740392T>ACA349610192TTNc.10361-2032A>T (n.10361-2032A>T)
c.12328A>T (p.Met4110Leu)
c.12127A>T (p.Met4043Leu)
c.11752A>T (p.Met3918Leu)
c.12841A>T (p.Met4281Leu)
c.11890A>T (p.Met3964Leu)
c.11938A>T (p.Met3980Leu)
c.11797A>T (p.Met3933Leu)
c.11893A>T (p.Met3965Leu)
c.10364-2032A>T (n.10364-2032A>T)
2g.178740392T>CCA349610188TTNc.10361-2032A>G (n.10361-2032A>G)
c.12328A>G (p.Met4110Val)
c.12127A>G (p.Met4043Val)
c.11752A>G (p.Met3918Val)
c.12841A>G (p.Met4281Val)
c.11890A>G (p.Met3964Val)
c.11938A>G (p.Met3980Val)
c.11797A>G (p.Met3933Val)
c.11893A>G (p.Met3965Val)
c.10364-2032A>G (n.10364-2032A>G)
2g.178740392T>GCA349610190TTNc.10361-2032A>C (n.10361-2032A>C)
c.12328A>C (p.Met4110Leu)
c.12127A>C (p.Met4043Leu)
c.11752A>C (p.Met3918Leu)
c.12841A>C (p.Met4281Leu)
c.11890A>C (p.Met3964Leu)
c.11938A>C (p.Met3980Leu)
c.11797A>C (p.Met3933Leu)
c.11893A>C (p.Met3965Leu)
c.10364-2032A>C (n.10364-2032A>C)
2g.178740393G>ACA430295978TTNc.10361-2033C>T (n.10361-2033C>T)
c.12327C>T (p.Val4109=)
c.12126C>T (p.Val4042=)
c.11751C>T (p.Val3917=)
c.12840C>T (p.Val4280=)
c.11889C>T (p.Val3963=)
c.11937C>T (p.Val3979=)
c.11796C>T (p.Val3932=)
c.11892C>T (p.Val3964=)
c.10364-2033C>T (n.10364-2033C>T)
COSMIC COSMIC
2g.178740393G>CCA430295979TTNc.10361-2033C>G (n.10361-2033C>G)
c.12327C>G (p.Val4109=)
c.12126C>G (p.Val4042=)
c.11751C>G (p.Val3917=)
c.12840C>G (p.Val4280=)
c.11889C>G (p.Val3963=)
c.11937C>G (p.Val3979=)
c.11796C>G (p.Val3932=)
c.11892C>G (p.Val3964=)
c.10364-2033C>G (n.10364-2033C>G)
2g.178740393G>TCA430295981TTNc.10361-2033C>A (n.10361-2033C>A)
c.12327C>A (p.Val4109=)
c.12126C>A (p.Val4042=)
c.11751C>A (p.Val3917=)
c.12840C>A (p.Val4280=)
c.11889C>A (p.Val3963=)
c.11937C>A (p.Val3979=)
c.11796C>A (p.Val3932=)
c.11892C>A (p.Val3964=)
c.10364-2033C>A (n.10364-2033C>A)
2g.178740394A>CCA349610193TTNc.10361-2034T>G (n.10361-2034T>G)
c.12326T>G (p.Val4109Gly)
c.12125T>G (p.Val4042Gly)
c.11750T>G (p.Val3917Gly)
c.12839T>G (p.Val4280Gly)
c.11888T>G (p.Val3963Gly)
c.11936T>G (p.Val3979Gly)
c.11795T>G (p.Val3932Gly)
c.11891T>G (p.Val3964Gly)
c.10364-2034T>G (n.10364-2034T>G)

Number of alleles fetched