Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.41933412C>ACA371064596KAT6Ac.4808G>T (p.Cys1603Phe)
c.4814G>T (p.Cys1605Phe)
c.3489G>T
c.4940G>T (p.Cys1647Phe)
c.4919G>T (p.Cys1640Phe)
c.4826G>T (p.Cys1609Phe)
c.3380G>T (p.Cys1127Phe)
8g.41933412C=CA1779195919KAT6Ac.4808G= (p.Cys1603=)
c.4814G= (p.Cys1605=)
c.3489G=
c.4940G= (p.Cys1647=)
c.4919G= (p.Cys1640=)
c.4826G= (p.Cys1609=)
c.3380G= (p.Cys1127=)
8g.41933412C>GCA371064597KAT6Ac.4808G>C (p.Cys1603Ser)
c.4814G>C (p.Cys1605Ser)
c.3489G>C
c.4940G>C (p.Cys1647Ser)
c.4919G>C (p.Cys1640Ser)
c.4826G>C (p.Cys1609Ser)
c.3380G>C (p.Cys1127Ser)
8g.41933412C>TCA4729421KAT6Ac.4808G>A (p.Cys1603Tyr)
c.4814G>A (p.Cys1605Tyr)
c.3489G>A
c.4940G>A (p.Cys1647Tyr)
c.4919G>A (p.Cys1640Tyr)
c.4826G>A (p.Cys1609Tyr)
c.3380G>A (p.Cys1127Tyr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.41933413A>CCA371064598KAT6Ac.4807T>G (p.Cys1603Gly)
c.4813T>G (p.Cys1605Gly)
c.3488T>G
c.4939T>G (p.Cys1647Gly)
c.4918T>G (p.Cys1640Gly)
c.4825T>G (p.Cys1609Gly)
c.3379T>G (p.Cys1127Gly)
8g.41933413A>GCA371064599KAT6Ac.4807T>C (p.Cys1603Arg)
c.4813T>C (p.Cys1605Arg)
c.3488T>C
c.4939T>C (p.Cys1647Arg)
c.4918T>C (p.Cys1640Arg)
c.4825T>C (p.Cys1609Arg)
c.3379T>C (p.Cys1127Arg)
8g.41933413A>TCA371064600KAT6Ac.4807T>A (p.Cys1603Ser)
c.4813T>A (p.Cys1605Ser)
c.3488T>A
c.4939T>A (p.Cys1647Ser)
c.4918T>A (p.Cys1640Ser)
c.4825T>A (p.Cys1609Ser)
c.3379T>A (p.Cys1127Ser)
8g.41933414G>ACA460783732KAT6Ac.4806C>T (p.Ser1602=)
c.4812C>T (p.Ser1604=)
c.3487C>T
c.4938C>T (p.Ser1646=)
c.4917C>T (p.Ser1639=)
c.4824C>T (p.Ser1608=)
c.3378C>T (p.Ser1126=)
dbSNP gnomAD v2 gnomAD v4 COSMIC
8g.41933414G>CCA371064601KAT6Ac.4806C>G (p.Ser1602Arg)
c.4812C>G (p.Ser1604Arg)
c.3487C>G
c.4938C>G (p.Ser1646Arg)
c.4917C>G (p.Ser1639Arg)
c.4824C>G (p.Ser1608Arg)
c.3378C>G (p.Ser1126Arg)
8g.41933414G=CA1779195920KAT6Ac.4806C= (p.Ser1602=)
c.4812C= (p.Ser1604=)
c.3487C=
c.4938C= (p.Ser1646=)
c.4917C= (p.Ser1639=)
c.4824C= (p.Ser1608=)
c.3378C= (p.Ser1126=)
8g.41933414G>TCA371064602KAT6Ac.4806C>A (p.Ser1602Arg)
c.4812C>A (p.Ser1604Arg)
c.3487C>A
c.4938C>A (p.Ser1646Arg)
c.4917C>A (p.Ser1639Arg)
c.4824C>A (p.Ser1608Arg)
c.3378C>A (p.Ser1126Arg)
8g.41933415C>ACA371064603KAT6Ac.4805G>T (p.Ser1602Ile)
c.4811G>T (p.Ser1604Ile)
c.3486G>T
c.4937G>T (p.Ser1646Ile)
c.4916G>T (p.Ser1639Ile)
c.4823G>T (p.Ser1608Ile)
c.3377G>T (p.Ser1126Ile)
8g.41933415C>GCA371064604KAT6Ac.4805G>C (p.Ser1602Thr)
c.4811G>C (p.Ser1604Thr)
c.3486G>C
c.4937G>C (p.Ser1646Thr)
c.4916G>C (p.Ser1639Thr)
c.4823G>C (p.Ser1608Thr)
c.3377G>C (p.Ser1126Thr)
8g.41933415C>TCA371064605KAT6Ac.4805G>A (p.Ser1602Asn)
c.4811G>A (p.Ser1604Asn)
c.3486G>A
c.4937G>A (p.Ser1646Asn)
c.4916G>A (p.Ser1639Asn)
c.4823G>A (p.Ser1608Asn)
c.3377G>A (p.Ser1126Asn)
8g.41933416T>ACA371064607KAT6Ac.4804A>T (p.Ser1602Cys)
c.4810A>T (p.Ser1604Cys)
c.3485A>T
c.4936A>T (p.Ser1646Cys)
c.4915A>T (p.Ser1639Cys)
c.4822A>T (p.Ser1608Cys)
c.3376A>T (p.Ser1126Cys)
8g.41933416T>CCA4729422KAT6Ac.4804A>G (p.Ser1602Gly)
c.4810A>G (p.Ser1604Gly)
c.3485A>G
c.4936A>G (p.Ser1646Gly)
c.4915A>G (p.Ser1639Gly)
c.4822A>G (p.Ser1608Gly)
c.3376A>G (p.Ser1126Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.41933416T>GCA371064606KAT6Ac.4804A>C (p.Ser1602Arg)
c.4810A>C (p.Ser1604Arg)
c.3485A>C
c.4936A>C (p.Ser1646Arg)
c.4915A>C (p.Ser1639Arg)
c.4822A>C (p.Ser1608Arg)
c.3376A>C (p.Ser1126Arg)
8g.41933416T=CA1779195921KAT6Ac.4804A= (p.Ser1602=)
c.4810A= (p.Ser1604=)
c.3485A=
c.4936A= (p.Ser1646=)
c.4915A= (p.Ser1639=)
c.4822A= (p.Ser1608=)
c.3376A= (p.Ser1126=)
8g.41933417G>ACA4729423KAT6Ac.4803C>T (p.Ser1601=)
c.4809C>T (p.Ser1603=)
c.3484C>T
c.4935C>T (p.Ser1645=)
c.4914C>T (p.Ser1638=)
c.4821C>T (p.Ser1607=)
c.3375C>T (p.Ser1125=)
dbSNP ExAC gnomAD v2 gnomAD v4
8g.41933417G>CCA371064608KAT6Ac.4803C>G (p.Ser1601Arg)
c.4809C>G (p.Ser1603Arg)
c.3484C>G
c.4935C>G (p.Ser1645Arg)
c.4914C>G (p.Ser1638Arg)
c.4821C>G (p.Ser1607Arg)
c.3375C>G (p.Ser1125Arg)
8g.41933417G=CA1779195922KAT6Ac.4803C= (p.Ser1601=)
c.4809C= (p.Ser1603=)
c.3484C=
c.4935C= (p.Ser1645=)
c.4914C= (p.Ser1638=)
c.4821C= (p.Ser1607=)
c.3375C= (p.Ser1125=)
8g.41933417G>TCA371064609KAT6Ac.4803C>A (p.Ser1601Arg)
c.4809C>A (p.Ser1603Arg)
c.3484C>A
c.4935C>A (p.Ser1645Arg)
c.4914C>A (p.Ser1638Arg)
c.4821C>A (p.Ser1607Arg)
c.3375C>A (p.Ser1125Arg)
dbSNP gnomAD v2 gnomAD v4
8g.41933418C>ACA371064610KAT6Ac.4802G>T (p.Ser1601Ile)
c.4808G>T (p.Ser1603Ile)
c.3483G>T
c.4934G>T (p.Ser1645Ile)
c.4913G>T (p.Ser1638Ile)
c.4820G>T (p.Ser1607Ile)
c.3374G>T (p.Ser1125Ile)
8g.41933418C>GCA371064611KAT6Ac.4802G>C (p.Ser1601Thr)
c.4808G>C (p.Ser1603Thr)
c.3483G>C
c.4934G>C (p.Ser1645Thr)
c.4913G>C (p.Ser1638Thr)
c.4820G>C (p.Ser1607Thr)
c.3374G>C (p.Ser1125Thr)
8g.41933418C>TCA371064612KAT6Ac.4802G>A (p.Ser1601Asn)
c.4808G>A (p.Ser1603Asn)
c.3483G>A
c.4934G>A (p.Ser1645Asn)
c.4913G>A (p.Ser1638Asn)
c.4820G>A (p.Ser1607Asn)
c.3374G>A (p.Ser1125Asn)
8g.41933419T>ACA371064613KAT6Ac.4801A>T (p.Ser1601Cys)
c.4807A>T (p.Ser1603Cys)
c.3482A>T
c.4933A>T (p.Ser1645Cys)
c.4912A>T (p.Ser1638Cys)
c.4819A>T (p.Ser1607Cys)
c.3373A>T (p.Ser1125Cys)
8g.41933419T>CCA4729424KAT6Ac.4801A>G (p.Ser1601Gly)
c.4807A>G (p.Ser1603Gly)
c.3482A>G
c.4933A>G (p.Ser1645Gly)
c.4912A>G (p.Ser1638Gly)
c.4819A>G (p.Ser1607Gly)
c.3373A>G (p.Ser1125Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.41933419T>GCA371064614KAT6Ac.4801A>C (p.Ser1601Arg)
c.4807A>C (p.Ser1603Arg)
c.3482A>C
c.4933A>C (p.Ser1645Arg)
c.4912A>C (p.Ser1638Arg)
c.4819A>C (p.Ser1607Arg)
c.3373A>C (p.Ser1125Arg)
8g.41933419T=CA1779195923KAT6Ac.4801A= (p.Ser1601=)
c.4807A= (p.Ser1603=)
c.3482A=
c.4933A= (p.Ser1645=)
c.4912A= (p.Ser1638=)
c.4819A= (p.Ser1607=)
c.3373A= (p.Ser1125=)
8g.41933420C>ACA371064615KAT6Ac.4800G>T (p.Gln1600His)
c.4806G>T (p.Gln1602His)
c.3481G>T
c.4932G>T (p.Gln1644His)
c.4911G>T (p.Gln1637His)
c.4818G>T (p.Gln1606His)
c.3372G>T (p.Gln1124His)
gnomAD v4
8g.41933420C>GCA371064616KAT6Ac.4800G>C (p.Gln1600His)
c.4806G>C (p.Gln1602His)
c.3481G>C
c.4932G>C (p.Gln1644His)
c.4911G>C (p.Gln1637His)
c.4818G>C (p.Gln1606His)
c.3372G>C (p.Gln1124His)
8g.41933420C>TCA460783739KAT6Ac.4800G>A (p.Gln1600=)
c.4806G>A (p.Gln1602=)
c.3481G>A
c.4932G>A (p.Gln1644=)
c.4911G>A (p.Gln1637=)
c.4818G>A (p.Gln1606=)
c.3372G>A (p.Gln1124=)
8g.41933421T>ACA371064617KAT6Ac.4799A>T (p.Gln1600Leu)
c.4805A>T (p.Gln1602Leu)
c.3480A>T
c.4931A>T (p.Gln1644Leu)
c.4910A>T (p.Gln1637Leu)
c.4817A>T (p.Gln1606Leu)
c.3371A>T (p.Gln1124Leu)
8g.41933421T>CCA371064618KAT6Ac.4799A>G (p.Gln1600Arg)
c.4805A>G (p.Gln1602Arg)
c.3480A>G
c.4931A>G (p.Gln1644Arg)
c.4910A>G (p.Gln1637Arg)
c.4817A>G (p.Gln1606Arg)
c.3371A>G (p.Gln1124Arg)
gnomAD v4
8g.41933421T>GCA371064619KAT6Ac.4799A>C (p.Gln1600Pro)
c.4805A>C (p.Gln1602Pro)
c.3480A>C
c.4931A>C (p.Gln1644Pro)
c.4910A>C (p.Gln1637Pro)
c.4817A>C (p.Gln1606Pro)
c.3371A>C (p.Gln1124Pro)
8g.41933422G>ACA371064621KAT6Ac.4798C>T (p.Gln1600Ter)
c.4804C>T (p.Gln1602Ter)
c.3479C>T
c.4930C>T (p.Gln1644Ter)
c.4909C>T (p.Gln1637Ter)
c.4816C>T (p.Gln1606Ter)
c.3370C>T (p.Gln1124Ter)
8g.41933422G>CCA4729425KAT6Ac.4798C>G (p.Gln1600Glu)
c.4804C>G (p.Gln1602Glu)
c.3479C>G
c.4930C>G (p.Gln1644Glu)
c.4909C>G (p.Gln1637Glu)
c.4816C>G (p.Gln1606Glu)
c.3370C>G (p.Gln1124Glu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.41933422G=CA1779195924KAT6Ac.4798C= (p.Gln1600=)
c.4804C= (p.Gln1602=)
c.3479C=
c.4930C= (p.Gln1644=)
c.4909C= (p.Gln1637=)
c.4816C= (p.Gln1606=)
c.3370C= (p.Gln1124=)
8g.41933422G>TCA371064620KAT6Ac.4798C>A (p.Gln1600Lys)
c.4804C>A (p.Gln1602Lys)
c.3479C>A
c.4930C>A (p.Gln1644Lys)
c.4909C>A (p.Gln1637Lys)
c.4816C>A (p.Gln1606Lys)
c.3370C>A (p.Gln1124Lys)
8g.41933423G>ACA460783746KAT6Ac.4797C>T (p.Thr1599=)
c.4803C>T (p.Thr1601=)
c.3478C>T
c.4929C>T (p.Thr1643=)
c.4908C>T (p.Thr1636=)
c.4815C>T (p.Thr1605=)
c.3369C>T (p.Thr1123=)
gnomAD v4
8g.41933423G>CCA460783748KAT6Ac.4797C>G (p.Thr1599=)
c.4803C>G (p.Thr1601=)
c.3478C>G
c.4929C>G (p.Thr1643=)
c.4908C>G (p.Thr1636=)
c.4815C>G (p.Thr1605=)
c.3369C>G (p.Thr1123=)
8g.41933423G>TCA460783747KAT6Ac.4797C>A (p.Thr1599=)
c.4803C>A (p.Thr1601=)
c.3478C>A
c.4929C>A (p.Thr1643=)
c.4908C>A (p.Thr1636=)
c.4815C>A (p.Thr1605=)
c.3369C>A (p.Thr1123=)
8g.41933424G>ACA371064622KAT6Ac.4796C>T (p.Thr1599Ile)
c.4802C>T (p.Thr1601Ile)
c.3477C>T
c.4928C>T (p.Thr1643Ile)
c.4907C>T (p.Thr1636Ile)
c.4814C>T (p.Thr1605Ile)
c.3368C>T (p.Thr1123Ile)
8g.41933424G>CCA371064623KAT6Ac.4796C>G (p.Thr1599Ser)
c.4802C>G (p.Thr1601Ser)
c.3477C>G
c.4928C>G (p.Thr1643Ser)
c.4907C>G (p.Thr1636Ser)
c.4814C>G (p.Thr1605Ser)
c.3368C>G (p.Thr1123Ser)
8g.41933424G>TCA371064624KAT6Ac.4796C>A (p.Thr1599Asn)
c.4802C>A (p.Thr1601Asn)
c.3477C>A
c.4928C>A (p.Thr1643Asn)
c.4907C>A (p.Thr1636Asn)
c.4814C>A (p.Thr1605Asn)
c.3368C>A (p.Thr1123Asn)
gnomAD v4
8g.41933424_41933430delinsGTGAGGCCA1779195925KAT6Ac.4790_4796delinsGCCTCAC (p.Ser1597=)
c.4796_4802delinsGCCTCAC (p.Ser1599=)
c.3471_3477delinsGCCTCAC
c.4922_4928delinsGCCTCAC (p.Ser1641=)
c.4901_4907delinsGCCTCAC (p.Ser1634=)
c.4808_4814delinsGCCTCAC (p.Ser1603=)
c.3362_3368delinsGCCTCAC (p.Ser1121=)
8g.41933425T>ACA4729427KAT6Ac.4795A>T (p.Thr1599Ser)
c.4801A>T (p.Thr1601Ser)
c.3476A>T
c.4927A>T (p.Thr1643Ser)
c.4906A>T (p.Thr1636Ser)
c.4813A>T (p.Thr1605Ser)
c.3367A>T (p.Thr1123Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.41933425T>CCA371064625KAT6Ac.4795A>G (p.Thr1599Ala)
c.4801A>G (p.Thr1601Ala)
c.3476A>G
c.4927A>G (p.Thr1643Ala)
c.4906A>G (p.Thr1636Ala)
c.4813A>G (p.Thr1605Ala)
c.3367A>G (p.Thr1123Ala)
8g.41933425T>GCA371064626KAT6Ac.4795A>C (p.Thr1599Pro)
c.4801A>C (p.Thr1601Pro)
c.3476A>C
c.4927A>C (p.Thr1643Pro)
c.4906A>C (p.Thr1636Pro)
c.4813A>C (p.Thr1605Pro)
c.3367A>C (p.Thr1123Pro)
8g.41933425T=CA1779195926KAT6Ac.4795A= (p.Thr1599=)
c.4801A= (p.Thr1601=)
c.3476A=
c.4927A= (p.Thr1643=)
c.4906A= (p.Thr1636=)
c.4813A= (p.Thr1605=)
c.3367A= (p.Thr1123=)
8g.41933427_41933432delCA4729426KAT6Ac.4790_4795del (p.Ser1597_Leu1598del)
c.4796_4801del (p.Ser1599_Leu1600del)
c.3471_3476del
c.4922_4927del (p.Ser1641_Leu1642del)
c.4901_4906del (p.Ser1634_Leu1635del)
c.4808_4813del (p.Ser1603_Leu1604del)
c.3362_3367del (p.Ser1121_Leu1122del)
dbSNP ExAC gnomAD v4
8g.41933426G>ACA460783756KAT6Ac.4794C>T (p.Leu1598=)
c.4800C>T (p.Leu1600=)
c.3475C>T
c.4926C>T (p.Leu1642=)
c.4905C>T (p.Leu1635=)
c.4812C>T (p.Leu1604=)
c.3366C>T (p.Leu1122=)
gnomAD v4
8g.41933426G>CCA460783754KAT6Ac.4794C>G (p.Leu1598=)
c.4800C>G (p.Leu1600=)
c.3475C>G
c.4926C>G (p.Leu1642=)
c.4905C>G (p.Leu1635=)
c.4812C>G (p.Leu1604=)
c.3366C>G (p.Leu1122=)
8g.41933426G>TCA460783755KAT6Ac.4794C>A (p.Leu1598=)
c.4800C>A (p.Leu1600=)
c.3475C>A
c.4926C>A (p.Leu1642=)
c.4905C>A (p.Leu1635=)
c.4812C>A (p.Leu1604=)
c.3366C>A (p.Leu1122=)
8g.41933427A>CCA371064629KAT6Ac.4793T>G (p.Leu1598Arg)
c.4799T>G (p.Leu1600Arg)
c.3474T>G
c.4925T>G (p.Leu1642Arg)
c.4904T>G (p.Leu1635Arg)
c.4811T>G (p.Leu1604Arg)
c.3365T>G (p.Leu1122Arg)
gnomAD v4
8g.41933427A>GCA371064627KAT6Ac.4793T>C (p.Leu1598Pro)
c.4799T>C (p.Leu1600Pro)
c.3474T>C
c.4925T>C (p.Leu1642Pro)
c.4904T>C (p.Leu1635Pro)
c.4811T>C (p.Leu1604Pro)
c.3365T>C (p.Leu1122Pro)
gnomAD v4
8g.41933427A>TCA371064628KAT6Ac.4793T>A (p.Leu1598His)
c.4799T>A (p.Leu1600His)
c.3474T>A
c.4925T>A (p.Leu1642His)
c.4904T>A (p.Leu1635His)
c.4811T>A (p.Leu1604His)
c.3365T>A (p.Leu1122His)
8g.41933428G>ACA371064630KAT6Ac.4792C>T (p.Leu1598Phe)
c.4798C>T (p.Leu1600Phe)
c.3473C>T
c.4924C>T (p.Leu1642Phe)
c.4903C>T (p.Leu1635Phe)
c.4810C>T (p.Leu1604Phe)
c.3364C>T (p.Leu1122Phe)
8g.41933428G>CCA371064631KAT6Ac.4792C>G (p.Leu1598Val)
c.4798C>G (p.Leu1600Val)
c.3473C>G
c.4924C>G (p.Leu1642Val)
c.4903C>G (p.Leu1635Val)
c.4810C>G (p.Leu1604Val)
c.3364C>G (p.Leu1122Val)
8g.41933428G=CA1779195927KAT6Ac.4792C= (p.Leu1598=)
c.4798C= (p.Leu1600=)
c.3473C=
c.4924C= (p.Leu1642=)
c.4903C= (p.Leu1635=)
c.4810C= (p.Leu1604=)
c.3364C= (p.Leu1122=)
8g.41933428G>TCA371064632KAT6Ac.4792C>A (p.Leu1598Ile)
c.4798C>A (p.Leu1600Ile)
c.3473C>A
c.4924C>A (p.Leu1642Ile)
c.4903C>A (p.Leu1635Ile)
c.4810C>A (p.Leu1604Ile)
c.3364C>A (p.Leu1122Ile)
ClinVar dbSNP gnomAD v3 gnomAD v4
8g.41933429G>ACA460783761KAT6Ac.4791C>T (p.Ser1597=)
c.4797C>T (p.Ser1599=)
c.3472C>T
c.4923C>T (p.Ser1641=)
c.4902C>T (p.Ser1634=)
c.4809C>T (p.Ser1603=)
c.3363C>T (p.Ser1121=)
8g.41933429G>CCA371064633KAT6Ac.4791C>G (p.Ser1597Arg)
c.4797C>G (p.Ser1599Arg)
c.3472C>G
c.4923C>G (p.Ser1641Arg)
c.4902C>G (p.Ser1634Arg)
c.4809C>G (p.Ser1603Arg)
c.3363C>G (p.Ser1121Arg)
8g.41933429G>TCA371064634KAT6Ac.4791C>A (p.Ser1597Arg)
c.4797C>A (p.Ser1599Arg)
c.3472C>A
c.4923C>A (p.Ser1641Arg)
c.4902C>A (p.Ser1634Arg)
c.4809C>A (p.Ser1603Arg)
c.3363C>A (p.Ser1121Arg)
8g.41933430C>ACA371064635KAT6Ac.4790G>T (p.Ser1597Ile)
c.4796G>T (p.Ser1599Ile)
c.3471G>T
c.4922G>T (p.Ser1641Ile)
c.4901G>T (p.Ser1634Ile)
c.4808G>T (p.Ser1603Ile)
c.3362G>T (p.Ser1121Ile)
8g.41933430C>GCA371064637KAT6Ac.4790G>C (p.Ser1597Thr)
c.4796G>C (p.Ser1599Thr)
c.3471G>C
c.4922G>C (p.Ser1641Thr)
c.4901G>C (p.Ser1634Thr)
c.4808G>C (p.Ser1603Thr)
c.3362G>C (p.Ser1121Thr)
gnomAD v4
8g.41933430C>TCA371064636KAT6Ac.4790G>A (p.Ser1597Asn)
c.4796G>A (p.Ser1599Asn)
c.3471G>A
c.4922G>A (p.Ser1641Asn)
c.4901G>A (p.Ser1634Asn)
c.4808G>A (p.Ser1603Asn)
c.3362G>A (p.Ser1121Asn)
COSMIC
8g.41933431T>ACA4729428KAT6Ac.4789A>T (p.Ser1597Cys)
c.4795A>T (p.Ser1599Cys)
c.3470A>T
c.4921A>T (p.Ser1641Cys)
c.4900A>T (p.Ser1634Cys)
c.4807A>T (p.Ser1603Cys)
c.3361A>T (p.Ser1121Cys)
dbSNP ExAC gnomAD v2 gnomAD v4
8g.41933431T>CCA371064638KAT6Ac.4789A>G (p.Ser1597Gly)
c.4795A>G (p.Ser1599Gly)
c.3470A>G
c.4921A>G (p.Ser1641Gly)
c.4900A>G (p.Ser1634Gly)
c.4807A>G (p.Ser1603Gly)
c.3361A>G (p.Ser1121Gly)
8g.41933431T>GCA371064639KAT6Ac.4789A>C (p.Ser1597Arg)
c.4795A>C (p.Ser1599Arg)
c.3470A>C
c.4921A>C (p.Ser1641Arg)
c.4900A>C (p.Ser1634Arg)
c.4807A>C (p.Ser1603Arg)
c.3361A>C (p.Ser1121Arg)
8g.41933431T=CA1779195928KAT6Ac.4789A= (p.Ser1597=)
c.4795A= (p.Ser1599=)
c.3470A=
c.4921A= (p.Ser1641=)
c.4900A= (p.Ser1634=)
c.4807A= (p.Ser1603=)
c.3361A= (p.Ser1121=)
8g.41933432G>ACA460783763KAT6Ac.4788C>T (p.Ser1596=)
c.4794C>T (p.Ser1598=)
c.3469C>T
c.4920C>T (p.Ser1640=)
c.4899C>T (p.Ser1633=)
c.4806C>T (p.Ser1602=)
c.3360C>T (p.Ser1120=)
dbSNP gnomAD v4
8g.41933432G>CCA371064640KAT6Ac.4788C>G (p.Ser1596Arg)
c.4794C>G (p.Ser1598Arg)
c.3469C>G
c.4920C>G (p.Ser1640Arg)
c.4899C>G (p.Ser1633Arg)
c.4806C>G (p.Ser1602Arg)
c.3360C>G (p.Ser1120Arg)
8g.41933432G=CA1779195929KAT6Ac.4788C= (p.Ser1596=)
c.4794C= (p.Ser1598=)
c.3469C=
c.4920C= (p.Ser1640=)
c.4899C= (p.Ser1633=)
c.4806C= (p.Ser1602=)
c.3360C= (p.Ser1120=)
8g.41933432G>TCA371064641KAT6Ac.4788C>A (p.Ser1596Arg)
c.4794C>A (p.Ser1598Arg)
c.3469C>A
c.4920C>A (p.Ser1640Arg)
c.4899C>A (p.Ser1633Arg)
c.4806C>A (p.Ser1602Arg)
c.3360C>A (p.Ser1120Arg)
gnomAD v4
8g.41933433C>ACA371064642KAT6Ac.4787G>T (p.Ser1596Ile)
c.4793G>T (p.Ser1598Ile)
c.3468G>T
c.4919G>T (p.Ser1640Ile)
c.4898G>T (p.Ser1633Ile)
c.4805G>T (p.Ser1602Ile)
c.3359G>T (p.Ser1120Ile)
8g.41933433C=CA1779195930KAT6Ac.4787G= (p.Ser1596=)
c.4793G= (p.Ser1598=)
c.3468G=
c.4919G= (p.Ser1640=)
c.4898G= (p.Ser1633=)
c.4805G= (p.Ser1602=)
c.3359G= (p.Ser1120=)
8g.41933433C>GCA371064643KAT6Ac.4787G>C (p.Ser1596Thr)
c.4793G>C (p.Ser1598Thr)
c.3468G>C
c.4919G>C (p.Ser1640Thr)
c.4898G>C (p.Ser1633Thr)
c.4805G>C (p.Ser1602Thr)
c.3359G>C (p.Ser1120Thr)
dbSNP
8g.41933433C>TCA371064644KAT6Ac.4787G>A (p.Ser1596Asn)
c.4793G>A (p.Ser1598Asn)
c.3468G>A
c.4919G>A (p.Ser1640Asn)
c.4898G>A (p.Ser1633Asn)
c.4805G>A (p.Ser1602Asn)
c.3359G>A (p.Ser1120Asn)
8g.41933434T>ACA371064645KAT6Ac.4786A>T (p.Ser1596Cys)
c.4792A>T (p.Ser1598Cys)
c.3467A>T
c.4918A>T (p.Ser1640Cys)
c.4897A>T (p.Ser1633Cys)
c.4804A>T (p.Ser1602Cys)
c.3358A>T (p.Ser1120Cys)
8g.41933434T>CCA371064646KAT6Ac.4786A>G (p.Ser1596Gly)
c.4792A>G (p.Ser1598Gly)
c.3467A>G
c.4918A>G (p.Ser1640Gly)
c.4897A>G (p.Ser1633Gly)
c.4804A>G (p.Ser1602Gly)
c.3358A>G (p.Ser1120Gly)
dbSNP gnomAD v2 gnomAD v4
8g.41933434T>GCA371064647KAT6Ac.4786A>C (p.Ser1596Arg)
c.4792A>C (p.Ser1598Arg)
c.3467A>C
c.4918A>C (p.Ser1640Arg)
c.4897A>C (p.Ser1633Arg)
c.4804A>C (p.Ser1602Arg)
c.3358A>C (p.Ser1120Arg)
8g.41933434T=CA1779195931KAT6Ac.4786A= (p.Ser1596=)
c.4792A= (p.Ser1598=)
c.3467A=
c.4918A= (p.Ser1640=)
c.4897A= (p.Ser1633=)
c.4804A= (p.Ser1602=)
c.3358A= (p.Ser1120=)
8g.41933435G>ACA460783768KAT6Ac.4785C>T (p.Ser1595=)
c.4791C>T (p.Ser1597=)
c.3466C>T
c.4917C>T (p.Ser1639=)
c.4896C>T (p.Ser1632=)
c.4803C>T (p.Ser1601=)
c.3357C>T (p.Ser1119=)
8g.41933435G>CCA460783769KAT6Ac.4785C>G (p.Ser1595=)
c.4791C>G (p.Ser1597=)
c.3466C>G
c.4917C>G (p.Ser1639=)
c.4896C>G (p.Ser1632=)
c.4803C>G (p.Ser1601=)
c.3357C>G (p.Ser1119=)
8g.41933435G>TCA460783770KAT6Ac.4785C>A (p.Ser1595=)
c.4791C>A (p.Ser1597=)
c.3466C>A
c.4917C>A (p.Ser1639=)
c.4896C>A (p.Ser1632=)
c.4803C>A (p.Ser1601=)
c.3357C>A (p.Ser1119=)
8g.41933436G>ACA371064648KAT6Ac.4784C>T (p.Ser1595Phe)
c.4790C>T (p.Ser1597Phe)
c.3465C>T
c.4916C>T (p.Ser1639Phe)
c.4895C>T (p.Ser1632Phe)
c.4802C>T (p.Ser1601Phe)
c.3356C>T (p.Ser1119Phe)
8g.41933436G>CCA371064650KAT6Ac.4784C>G (p.Ser1595Cys)
c.4790C>G (p.Ser1597Cys)
c.3465C>G
c.4916C>G (p.Ser1639Cys)
c.4895C>G (p.Ser1632Cys)
c.4802C>G (p.Ser1601Cys)
c.3356C>G (p.Ser1119Cys)
8g.41933436G>TCA371064649KAT6Ac.4784C>A (p.Ser1595Tyr)
c.4790C>A (p.Ser1597Tyr)
c.3465C>A
c.4916C>A (p.Ser1639Tyr)
c.4895C>A (p.Ser1632Tyr)
c.4802C>A (p.Ser1601Tyr)
c.3356C>A (p.Ser1119Tyr)
8g.41933437A=CA1779195932KAT6Ac.4783T= (p.Ser1595=)
c.4789T= (p.Ser1597=)
c.3464T=
c.4915T= (p.Ser1639=)
c.4894T= (p.Ser1632=)
c.4801T= (p.Ser1601=)
c.3355T= (p.Ser1119=)
8g.41933437A>CCA371064651KAT6Ac.4783T>G (p.Ser1595Ala)
c.4789T>G (p.Ser1597Ala)
c.3464T>G
c.4915T>G (p.Ser1639Ala)
c.4894T>G (p.Ser1632Ala)
c.4801T>G (p.Ser1601Ala)
c.3355T>G (p.Ser1119Ala)
8g.41933437A>GCA371064653KAT6Ac.4783T>C (p.Ser1595Pro)
c.4789T>C (p.Ser1597Pro)
c.3464T>C
c.4915T>C (p.Ser1639Pro)
c.4894T>C (p.Ser1632Pro)
c.4801T>C (p.Ser1601Pro)
c.3355T>C (p.Ser1119Pro)
dbSNP
8g.41933437A>TCA371064652KAT6Ac.4783T>A (p.Ser1595Thr)
c.4789T>A (p.Ser1597Thr)
c.3464T>A
c.4915T>A (p.Ser1639Thr)
c.4894T>A (p.Ser1632Thr)
c.4801T>A (p.Ser1601Thr)
c.3355T>A (p.Ser1119Thr)
8g.41933438G>ACA460783772KAT6Ac.4782C>T (p.Ser1594=)
c.4788C>T (p.Ser1596=)
c.3463C>T
c.4914C>T (p.Ser1638=)
c.4893C>T (p.Ser1631=)
c.4800C>T (p.Ser1600=)
c.3354C>T (p.Ser1118=)
gnomAD v4
8g.41933438G>CCA460783773KAT6Ac.4782C>G (p.Ser1594=)
c.4788C>G (p.Ser1596=)
c.3463C>G
c.4914C>G (p.Ser1638=)
c.4893C>G (p.Ser1631=)
c.4800C>G (p.Ser1600=)
c.3354C>G (p.Ser1118=)
8g.41933438G>TCA460783774KAT6Ac.4782C>A (p.Ser1594=)
c.4788C>A (p.Ser1596=)
c.3463C>A
c.4914C>A (p.Ser1638=)
c.4893C>A (p.Ser1631=)
c.4800C>A (p.Ser1600=)
c.3354C>A (p.Ser1118=)
8g.41933438_41933441delinsGGACCA1779195933KAT6Ac.4779_4782delinsGTCC (p.Ser1593=)
c.4785_4788delinsGTCC (p.Ser1595=)
c.3460_3463delinsGTCC
c.4911_4914delinsGTCC (p.Ser1637=)
c.4890_4893delinsGTCC (p.Ser1630=)
c.4797_4800delinsGTCC (p.Ser1599=)
c.3351_3354delinsGTCC (p.Ser1117=)
8g.41933439G>ACA371064654KAT6Ac.4781C>T (p.Ser1594Phe)
c.4787C>T (p.Ser1596Phe)
c.3462C>T
c.4913C>T (p.Ser1638Phe)
c.4892C>T (p.Ser1631Phe)
c.4799C>T (p.Ser1600Phe)
c.3353C>T (p.Ser1118Phe)
8g.41933439G>CCA371064655KAT6Ac.4781C>G (p.Ser1594Cys)
c.4787C>G (p.Ser1596Cys)
c.3462C>G
c.4913C>G (p.Ser1638Cys)
c.4892C>G (p.Ser1631Cys)
c.4799C>G (p.Ser1600Cys)
c.3353C>G (p.Ser1118Cys)
8g.41933439G>TCA371064656KAT6Ac.4781C>A (p.Ser1594Tyr)
c.4787C>A (p.Ser1596Tyr)
c.3462C>A
c.4913C>A (p.Ser1638Tyr)
c.4892C>A (p.Ser1631Tyr)
c.4799C>A (p.Ser1600Tyr)
c.3353C>A (p.Ser1118Tyr)
8g.41933442_41933444delCA4729429KAT6Ac.4779_4781del (p.Ser1594del)
c.4785_4787del (p.Ser1596del)
c.3460_3462del
c.4911_4913del (p.Ser1638del)
c.4890_4892del (p.Ser1631del)
c.4797_4799del (p.Ser1600del)
c.3351_3353del (p.Ser1118del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.41933440A=CA1779195934KAT6Ac.4780T= (p.Ser1594=)
c.4786T= (p.Ser1596=)
c.3461T=
c.4912T= (p.Ser1638=)
c.4891T= (p.Ser1631=)
c.4798T= (p.Ser1600=)
c.3352T= (p.Ser1118=)
8g.41933440A>CCA371064657KAT6Ac.4780T>G (p.Ser1594Ala)
c.4786T>G (p.Ser1596Ala)
c.3461T>G
c.4912T>G (p.Ser1638Ala)
c.4891T>G (p.Ser1631Ala)
c.4798T>G (p.Ser1600Ala)
c.3352T>G (p.Ser1118Ala)
8g.41933440A>GCA371064658KAT6Ac.4780T>C (p.Ser1594Pro)
c.4786T>C (p.Ser1596Pro)
c.3461T>C
c.4912T>C (p.Ser1638Pro)
c.4891T>C (p.Ser1631Pro)
c.4798T>C (p.Ser1600Pro)
c.3352T>C (p.Ser1118Pro)
dbSNP
8g.41933440A>TCA371064659KAT6Ac.4780T>A (p.Ser1594Thr)
c.4786T>A (p.Ser1596Thr)
c.3461T>A
c.4912T>A (p.Ser1638Thr)
c.4891T>A (p.Ser1631Thr)
c.4798T>A (p.Ser1600Thr)
c.3352T>A (p.Ser1118Thr)
8g.41933441C>ACA460783776KAT6Ac.4779G>T (p.Ser1593=)
c.4785G>T (p.Ser1595=)
c.3460G>T
c.4911G>T (p.Ser1637=)
c.4890G>T (p.Ser1630=)
c.4797G>T (p.Ser1599=)
c.3351G>T (p.Ser1117=)
dbSNP gnomAD v3 gnomAD v4
8g.41933441C=CA1779195935KAT6Ac.4779G= (p.Ser1593=)
c.4785G= (p.Ser1595=)
c.3460G=
c.4911G= (p.Ser1637=)
c.4890G= (p.Ser1630=)
c.4797G= (p.Ser1599=)
c.3351G= (p.Ser1117=)
8g.41933441C>GCA460783775KAT6Ac.4779G>C (p.Ser1593=)
c.4785G>C (p.Ser1595=)
c.3460G>C
c.4911G>C (p.Ser1637=)
c.4890G>C (p.Ser1630=)
c.4797G>C (p.Ser1599=)
c.3351G>C (p.Ser1117=)
8g.41933441C>TCA4729430KAT6Ac.4779G>A (p.Ser1593=)
c.4785G>A (p.Ser1595=)
c.3460G>A
c.4911G>A (p.Ser1637=)
c.4890G>A (p.Ser1630=)
c.4797G>A (p.Ser1599=)
c.3351G>A (p.Ser1117=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.41933442G>ACA371064660KAT6Ac.4778C>T (p.Ser1593Leu)
c.4784C>T (p.Ser1595Leu)
c.3459C>T
c.4910C>T (p.Ser1637Leu)
c.4889C>T (p.Ser1630Leu)
c.4796C>T (p.Ser1599Leu)
c.3350C>T (p.Ser1117Leu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.41933442G>CCA371064661KAT6Ac.4778C>G (p.Ser1593Trp)
c.4784C>G (p.Ser1595Trp)
c.3459C>G
c.4910C>G (p.Ser1637Trp)
c.4889C>G (p.Ser1630Trp)
c.4796C>G (p.Ser1599Trp)
c.3350C>G (p.Ser1117Trp)
8g.41933442G=CA1779195936KAT6Ac.4778C= (p.Ser1593=)
c.4784C= (p.Ser1595=)
c.3459C=
c.4910C= (p.Ser1637=)
c.4889C= (p.Ser1630=)
c.4796C= (p.Ser1599=)
c.3350C= (p.Ser1117=)
8g.41933442G>TCA371064662KAT6Ac.4778C>A (p.Ser1593Ter)
c.4784C>A (p.Ser1595Ter)
c.3459C>A
c.4910C>A (p.Ser1637Ter)
c.4889C>A (p.Ser1630Ter)
c.4796C>A (p.Ser1599Ter)
c.3350C>A (p.Ser1117Ter)
8g.41933443A>CCA371064665KAT6Ac.4777T>G (p.Ser1593Ala)
c.4783T>G (p.Ser1595Ala)
c.3458T>G
c.4909T>G (p.Ser1637Ala)
c.4888T>G (p.Ser1630Ala)
c.4795T>G (p.Ser1599Ala)
c.3349T>G (p.Ser1117Ala)
8g.41933443A>GCA371064664KAT6Ac.4777T>C (p.Ser1593Pro)
c.4783T>C (p.Ser1595Pro)
c.3458T>C
c.4909T>C (p.Ser1637Pro)
c.4888T>C (p.Ser1630Pro)
c.4795T>C (p.Ser1599Pro)
c.3349T>C (p.Ser1117Pro)
gnomAD v4
8g.41933443A>TCA371064663KAT6Ac.4777T>A (p.Ser1593Thr)
c.4783T>A (p.Ser1595Thr)
c.3458T>A
c.4909T>A (p.Ser1637Thr)
c.4888T>A (p.Ser1630Thr)
c.4795T>A (p.Ser1599Thr)
c.3349T>A (p.Ser1117Thr)
8g.41933444C>ACA460783777KAT6Ac.4776G>T (p.Leu1592=)
c.4782G>T (p.Leu1594=)
c.3457G>T
c.4908G>T (p.Leu1636=)
c.4887G>T (p.Leu1629=)
c.4794G>T (p.Leu1598=)
c.3348G>T (p.Leu1116=)
8g.41933444C>GCA460783778KAT6Ac.4776G>C (p.Leu1592=)
c.4782G>C (p.Leu1594=)
c.3457G>C
c.4908G>C (p.Leu1636=)
c.4887G>C (p.Leu1629=)
c.4794G>C (p.Leu1598=)
c.3348G>C (p.Leu1116=)
8g.41933444C>TCA460783779KAT6Ac.4776G>A (p.Leu1592=)
c.4782G>A (p.Leu1594=)
c.3457G>A
c.4908G>A (p.Leu1636=)
c.4887G>A (p.Leu1629=)
c.4794G>A (p.Leu1598=)
c.3348G>A (p.Leu1116=)
gnomAD v4
8g.41933445A>CCA371064666KAT6Ac.4775T>G (p.Leu1592Arg)
c.4781T>G (p.Leu1594Arg)
c.3456T>G
c.4907T>G (p.Leu1636Arg)
c.4886T>G (p.Leu1629Arg)
c.4793T>G (p.Leu1598Arg)
c.3347T>G (p.Leu1116Arg)
gnomAD v4
8g.41933445A>GCA371064667KAT6Ac.4775T>C (p.Leu1592Pro)
c.4781T>C (p.Leu1594Pro)
c.3456T>C
c.4907T>C (p.Leu1636Pro)
c.4886T>C (p.Leu1629Pro)
c.4793T>C (p.Leu1598Pro)
c.3347T>C (p.Leu1116Pro)
8g.41933445A>TCA371064668KAT6Ac.4775T>A (p.Leu1592Gln)
c.4781T>A (p.Leu1594Gln)
c.3456T>A
c.4907T>A (p.Leu1636Gln)
c.4886T>A (p.Leu1629Gln)
c.4793T>A (p.Leu1598Gln)
c.3347T>A (p.Leu1116Gln)
ClinVar
8g.41933446G>ACA460783782KAT6Ac.4774C>T (p.Leu1592=)
c.4780C>T (p.Leu1594=)
c.3455C>T
c.4906C>T (p.Leu1636=)
c.4885C>T (p.Leu1629=)
c.4792C>T (p.Leu1598=)
c.3346C>T (p.Leu1116=)
ClinVar dbSNP gnomAD v2 gnomAD v4
8g.41933446G>CCA371064669KAT6Ac.4774C>G (p.Leu1592Val)
c.4780C>G (p.Leu1594Val)
c.3455C>G
c.4906C>G (p.Leu1636Val)
c.4885C>G (p.Leu1629Val)
c.4792C>G (p.Leu1598Val)
c.3346C>G (p.Leu1116Val)
8g.41933446G=CA1779195937KAT6Ac.4774C= (p.Leu1592=)
c.4780C= (p.Leu1594=)
c.3455C=
c.4906C= (p.Leu1636=)
c.4885C= (p.Leu1629=)
c.4792C= (p.Leu1598=)
c.3346C= (p.Leu1116=)
8g.41933446G>TCA371064670KAT6Ac.4774C>A (p.Leu1592Met)
c.4780C>A (p.Leu1594Met)
c.3455C>A
c.4906C>A (p.Leu1636Met)
c.4885C>A (p.Leu1629Met)
c.4792C>A (p.Leu1598Met)
c.3346C>A (p.Leu1116Met)
8g.41933447C>ACA460783783KAT6Ac.4773G>T (p.Gly1591=)
c.4779G>T (p.Gly1593=)
c.3454G>T
c.4905G>T (p.Gly1635=)
c.4884G>T (p.Gly1628=)
c.4791G>T (p.Gly1597=)
c.3345G>T (p.Gly1115=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.41933447C=CA1779195938KAT6Ac.4773G= (p.Gly1591=)
c.4779G= (p.Gly1593=)
c.3454G=
c.4905G= (p.Gly1635=)
c.4884G= (p.Gly1628=)
c.4791G= (p.Gly1597=)
c.3345G= (p.Gly1115=)
8g.41933447C>GCA460783785KAT6Ac.4773G>C (p.Gly1591=)
c.4779G>C (p.Gly1593=)
c.3454G>C
c.4905G>C (p.Gly1635=)
c.4884G>C (p.Gly1628=)
c.4791G>C (p.Gly1597=)
c.3345G>C (p.Gly1115=)
8g.41933447C>TCA460783784KAT6Ac.4773G>A (p.Gly1591=)
c.4779G>A (p.Gly1593=)
c.3454G>A
c.4905G>A (p.Gly1635=)
c.4884G>A (p.Gly1628=)
c.4791G>A (p.Gly1597=)
c.3345G>A (p.Gly1115=)
8g.41933448C>ACA371064671KAT6Ac.4772G>T (p.Gly1591Val)
c.4778G>T (p.Gly1593Val)
c.3453G>T
c.4904G>T (p.Gly1635Val)
c.4883G>T (p.Gly1628Val)
c.4790G>T (p.Gly1597Val)
c.3344G>T (p.Gly1115Val)
dbSNP gnomAD v2 gnomAD v4 COSMIC
8g.41933448C=CA1779195939KAT6Ac.4772G= (p.Gly1591=)
c.4778G= (p.Gly1593=)
c.3453G=
c.4904G= (p.Gly1635=)
c.4883G= (p.Gly1628=)
c.4790G= (p.Gly1597=)
c.3344G= (p.Gly1115=)
8g.41933448C>GCA371064672KAT6Ac.4772G>C (p.Gly1591Ala)
c.4778G>C (p.Gly1593Ala)
c.3453G>C
c.4904G>C (p.Gly1635Ala)
c.4883G>C (p.Gly1628Ala)
c.4790G>C (p.Gly1597Ala)
c.3344G>C (p.Gly1115Ala)
8g.41933448C>TCA371064673KAT6Ac.4772G>A (p.Gly1591Glu)
c.4778G>A (p.Gly1593Glu)
c.3453G>A
c.4904G>A (p.Gly1635Glu)
c.4883G>A (p.Gly1628Glu)
c.4790G>A (p.Gly1597Glu)
c.3344G>A (p.Gly1115Glu)
8g.41933450_41933452dupCA2687076956KAT6Ac.4770_4772dup (p.Gly1591_Leu1592insGly)
c.4776_4778dup (p.Gly1593_Leu1594insGly)
c.3451_3453dup
c.4902_4904dup (p.Gly1635_Leu1636insGly)
c.4881_4883dup (p.Gly1628_Leu1629insGly)
c.4788_4790dup (p.Gly1597_Leu1598insGly)
c.3342_3344dup (p.Gly1115_Leu1116insGly)
gnomAD v4
8g.41933449C>ACA371064674KAT6Ac.4771G>T (p.Gly1591Trp)
c.4777G>T (p.Gly1593Trp)
c.3452G>T
c.4903G>T (p.Gly1635Trp)
c.4882G>T (p.Gly1628Trp)
c.4789G>T (p.Gly1597Trp)
c.3343G>T (p.Gly1115Trp)
8g.41933449C=CA1779195940KAT6Ac.4771G= (p.Gly1591=)
c.4777G= (p.Gly1593=)
c.3452G=
c.4903G= (p.Gly1635=)
c.4882G= (p.Gly1628=)
c.4789G= (p.Gly1597=)
c.3343G= (p.Gly1115=)
8g.41933449C>GCA371064675KAT6Ac.4771G>C (p.Gly1591Arg)
c.4777G>C (p.Gly1593Arg)
c.3452G>C
c.4903G>C (p.Gly1635Arg)
c.4882G>C (p.Gly1628Arg)
c.4789G>C (p.Gly1597Arg)
c.3343G>C (p.Gly1115Arg)
8g.41933449C>TCA371064676KAT6Ac.4771G>A (p.Gly1591Arg)
c.4777G>A (p.Gly1593Arg)
c.3452G>A
c.4903G>A (p.Gly1635Arg)
c.4882G>A (p.Gly1628Arg)
c.4789G>A (p.Gly1597Arg)
c.3343G>A (p.Gly1115Arg)
dbSNP gnomAD v2
8g.41933450A>CCA460783787KAT6Ac.4770T>G (p.Gly1590=)
c.4776T>G (p.Gly1592=)
c.3451T>G
c.4902T>G (p.Gly1634=)
c.4881T>G (p.Gly1627=)
c.4788T>G (p.Gly1596=)
c.3342T>G (p.Gly1114=)
8g.41933450A>GCA460783789KAT6Ac.4770T>C (p.Gly1590=)
c.4776T>C (p.Gly1592=)
c.3451T>C
c.4902T>C (p.Gly1634=)
c.4881T>C (p.Gly1627=)
c.4788T>C (p.Gly1596=)
c.3342T>C (p.Gly1114=)
8g.41933450A>TCA460783791KAT6Ac.4770T>A (p.Gly1590=)
c.4776T>A (p.Gly1592=)
c.3451T>A
c.4902T>A (p.Gly1634=)
c.4881T>A (p.Gly1627=)
c.4788T>A (p.Gly1596=)
c.3342T>A (p.Gly1114=)
8g.41933451C>ACA4729431KAT6Ac.4769G>T (p.Gly1590Val)
c.4775G>T (p.Gly1592Val)
c.3450G>T
c.4901G>T (p.Gly1634Val)
c.4880G>T (p.Gly1627Val)
c.4787G>T (p.Gly1596Val)
c.3341G>T (p.Gly1114Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.41933451C=CA1779195941KAT6Ac.4769G= (p.Gly1590=)
c.4775G= (p.Gly1592=)
c.3450G=
c.4901G= (p.Gly1634=)
c.4880G= (p.Gly1627=)
c.4787G= (p.Gly1596=)
c.3341G= (p.Gly1114=)
8g.41933451C>GCA371064678KAT6Ac.4769G>C (p.Gly1590Ala)
c.4775G>C (p.Gly1592Ala)
c.3450G>C
c.4901G>C (p.Gly1634Ala)
c.4880G>C (p.Gly1627Ala)
c.4787G>C (p.Gly1596Ala)
c.3341G>C (p.Gly1114Ala)
dbSNP gnomAD v2 gnomAD v4
8g.41933451C>TCA371064677KAT6Ac.4769G>A (p.Gly1590Asp)
c.4775G>A (p.Gly1592Asp)
c.3450G>A
c.4901G>A (p.Gly1634Asp)
c.4880G>A (p.Gly1627Asp)
c.4787G>A (p.Gly1596Asp)
c.3341G>A (p.Gly1114Asp)
8g.41933452C>ACA371064679KAT6Ac.4768G>T (p.Gly1590Cys)
c.4774G>T (p.Gly1592Cys)
c.3449G>T
c.4900G>T (p.Gly1634Cys)
c.4879G>T (p.Gly1627Cys)
c.4786G>T (p.Gly1596Cys)
c.3340G>T (p.Gly1114Cys)
dbSNP gnomAD v2 gnomAD v4
8g.41933452C=CA1779195942KAT6Ac.4768G= (p.Gly1590=)
c.4774G= (p.Gly1592=)
c.3449G=
c.4900G= (p.Gly1634=)
c.4879G= (p.Gly1627=)
c.4786G= (p.Gly1596=)
c.3340G= (p.Gly1114=)
8g.41933452C>GCA371064680KAT6Ac.4768G>C (p.Gly1590Arg)
c.4774G>C (p.Gly1592Arg)
c.3449G>C
c.4900G>C (p.Gly1634Arg)
c.4879G>C (p.Gly1627Arg)
c.4786G>C (p.Gly1596Arg)
c.3340G>C (p.Gly1114Arg)
ClinVar gnomAD v4
8g.41933452C>TCA4729432KAT6Ac.4768G>A (p.Gly1590Ser)
c.4774G>A (p.Gly1592Ser)
c.3449G>A
c.4900G>A (p.Gly1634Ser)
c.4879G>A (p.Gly1627Ser)
c.4786G>A (p.Gly1596Ser)
c.3340G>A (p.Gly1114Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.41933453G>ACA4729433KAT6Ac.4767C>T (p.Tyr1589=)
c.4773C>T (p.Tyr1591=)
c.3448C>T
c.4899C>T (p.Tyr1633=)
c.4878C>T (p.Tyr1626=)
c.4785C>T (p.Tyr1595=)
c.3339C>T (p.Tyr1113=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
8g.41933453G>CCA371064681KAT6Ac.4767C>G (p.Tyr1589Ter)
c.4773C>G (p.Tyr1591Ter)
c.3448C>G
c.4899C>G (p.Tyr1633Ter)
c.4878C>G (p.Tyr1626Ter)
c.4785C>G (p.Tyr1595Ter)
c.3339C>G (p.Tyr1113Ter)
8g.41933453G=CA1779195943KAT6Ac.4767C= (p.Tyr1589=)
c.4773C= (p.Tyr1591=)
c.3448C=
c.4899C= (p.Tyr1633=)
c.4878C= (p.Tyr1626=)
c.4785C= (p.Tyr1595=)
c.3339C= (p.Tyr1113=)
8g.41933453G>TCA371064682KAT6Ac.4767C>A (p.Tyr1589Ter)
c.4773C>A (p.Tyr1591Ter)
c.3448C>A
c.4899C>A (p.Tyr1633Ter)
c.4878C>A (p.Tyr1626Ter)
c.4785C>A (p.Tyr1595Ter)
c.3339C>A (p.Tyr1113Ter)
8g.41933453dupCA2739290069KAT6Ac.4767dup (p.Gly1590ArgfsTer?)
c.4773dup (p.Gly1592ArgfsTer?)
c.3448dup
c.4899dup (p.Gly1634ArgfsTer?)
c.4878dup (p.Gly1627ArgfsTer?)
c.4785dup (p.Gly1596ArgfsTer?)
c.3339dup (p.Gly1114ArgfsTer?)
8g.41933454T>ACA371064683KAT6Ac.4766A>T (p.Tyr1589Phe)
c.4772A>T (p.Tyr1591Phe)
c.3447A>T
c.4898A>T (p.Tyr1633Phe)
c.4877A>T (p.Tyr1626Phe)
c.4784A>T (p.Tyr1595Phe)
c.3338A>T (p.Tyr1113Phe)
gnomAD v4
8g.41933454T>CCA4729434KAT6Ac.4766A>G (p.Tyr1589Cys)
c.4772A>G (p.Tyr1591Cys)
c.3447A>G
c.4898A>G (p.Tyr1633Cys)
c.4877A>G (p.Tyr1626Cys)
c.4784A>G (p.Tyr1595Cys)
c.3338A>G (p.Tyr1113Cys)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
8g.41933454T>GCA371064684KAT6Ac.4766A>C (p.Tyr1589Ser)
c.4772A>C (p.Tyr1591Ser)
c.3447A>C
c.4898A>C (p.Tyr1633Ser)
c.4877A>C (p.Tyr1626Ser)
c.4784A>C (p.Tyr1595Ser)
c.3338A>C (p.Tyr1113Ser)
8g.41933454T=CA1779195944KAT6Ac.4766A= (p.Tyr1589=)
c.4772A= (p.Tyr1591=)
c.3447A=
c.4898A= (p.Tyr1633=)
c.4877A= (p.Tyr1626=)
c.4784A= (p.Tyr1595=)
c.3338A= (p.Tyr1113=)
8g.41933455A>CCA371064685KAT6Ac.4765T>G (p.Tyr1589Asp)
c.4771T>G (p.Tyr1591Asp)
c.3446T>G
c.4897T>G (p.Tyr1633Asp)
c.4876T>G (p.Tyr1626Asp)
c.4783T>G (p.Tyr1595Asp)
c.3337T>G (p.Tyr1113Asp)
8g.41933455A>GCA371064686KAT6Ac.4765T>C (p.Tyr1589His)
c.4771T>C (p.Tyr1591His)
c.3446T>C
c.4897T>C (p.Tyr1633His)
c.4876T>C (p.Tyr1626His)
c.4783T>C (p.Tyr1595His)
c.3337T>C (p.Tyr1113His)
8g.41933455A>TCA371064687KAT6Ac.4765T>A (p.Tyr1589Asn)
c.4771T>A (p.Tyr1591Asn)
c.3446T>A
c.4897T>A (p.Tyr1633Asn)
c.4876T>A (p.Tyr1626Asn)
c.4783T>A (p.Tyr1595Asn)
c.3337T>A (p.Tyr1113Asn)
8g.41933456G>ACA460783796KAT6Ac.4764C>T (p.Ser1588=)
c.4770C>T (p.Ser1590=)
c.3445C>T
c.4896C>T (p.Ser1632=)
c.4875C>T (p.Ser1625=)
c.4782C>T (p.Ser1594=)
c.3336C>T (p.Ser1112=)
dbSNP
8g.41933456G>CCA460783795KAT6Ac.4764C>G (p.Ser1588=)
c.4770C>G (p.Ser1590=)
c.3445C>G
c.4896C>G (p.Ser1632=)
c.4875C>G (p.Ser1625=)
c.4782C>G (p.Ser1594=)
c.3336C>G (p.Ser1112=)
dbSNP gnomAD v3 gnomAD v4
8g.41933456G=CA1779195945KAT6Ac.4764C= (p.Ser1588=)
c.4770C= (p.Ser1590=)
c.3445C=
c.4896C= (p.Ser1632=)
c.4875C= (p.Ser1625=)
c.4782C= (p.Ser1594=)
c.3336C= (p.Ser1112=)
8g.41933456G>TCA460783794KAT6Ac.4764C>A (p.Ser1588=)
c.4770C>A (p.Ser1590=)
c.3445C>A
c.4896C>A (p.Ser1632=)
c.4875C>A (p.Ser1625=)
c.4782C>A (p.Ser1594=)
c.3336C>A (p.Ser1112=)
8g.41933456_41933457delinsAACA645564873KAT6Ac.4763_4764delinsTT (p.Ser1588Phe)
c.4769_4770delinsTT (p.Ser1590Phe)
c.3444_3445delinsTT
c.4895_4896delinsTT (p.Ser1632Phe)
c.4874_4875delinsTT (p.Ser1625Phe)
c.4781_4782delinsTT (p.Ser1594Phe)
c.3335_3336delinsTT (p.Ser1112Phe)
COSMIC
8g.41933457G>ACA371064690KAT6Ac.4763C>T (p.Ser1588Phe)
c.4769C>T (p.Ser1590Phe)
c.3444C>T
c.4895C>T (p.Ser1632Phe)
c.4874C>T (p.Ser1625Phe)
c.4781C>T (p.Ser1594Phe)
c.3335C>T (p.Ser1112Phe)
dbSNP gnomAD v3 gnomAD v4
8g.41933457G>CCA371064689KAT6Ac.4763C>G (p.Ser1588Cys)
c.4769C>G (p.Ser1590Cys)
c.3444C>G
c.4895C>G (p.Ser1632Cys)
c.4874C>G (p.Ser1625Cys)
c.4781C>G (p.Ser1594Cys)
c.3335C>G (p.Ser1112Cys)
8g.41933457G>TCA371064688KAT6Ac.4763C>A (p.Ser1588Tyr)
c.4769C>A (p.Ser1590Tyr)
c.3444C>A
c.4895C>A (p.Ser1632Tyr)
c.4874C>A (p.Ser1625Tyr)
c.4781C>A (p.Ser1594Tyr)
c.3335C>A (p.Ser1112Tyr)
8g.41933458A>CCA371064691KAT6Ac.4762T>G (p.Ser1588Ala)
c.4768T>G (p.Ser1590Ala)
c.3443T>G
c.4894T>G (p.Ser1632Ala)
c.4873T>G (p.Ser1625Ala)
c.4780T>G (p.Ser1594Ala)
c.3334T>G (p.Ser1112Ala)
8g.41933458A>GCA371064692KAT6Ac.4762T>C (p.Ser1588Pro)
c.4768T>C (p.Ser1590Pro)
c.3443T>C
c.4894T>C (p.Ser1632Pro)
c.4873T>C (p.Ser1625Pro)
c.4780T>C (p.Ser1594Pro)
c.3334T>C (p.Ser1112Pro)
gnomAD v4
8g.41933458A>TCA371064693KAT6Ac.4762T>A (p.Ser1588Thr)
c.4768T>A (p.Ser1590Thr)
c.3443T>A
c.4894T>A (p.Ser1632Thr)
c.4873T>A (p.Ser1625Thr)
c.4780T>A (p.Ser1594Thr)
c.3334T>A (p.Ser1112Thr)
8g.41933459G>ACA460783799KAT6Ac.4761C>T (p.Cys1587=)
c.4767C>T (p.Cys1589=)
c.3442C>T
c.4893C>T (p.Cys1631=)
c.4872C>T (p.Cys1624=)
c.4779C>T (p.Cys1593=)
c.3333C>T (p.Cys1111=)
gnomAD v4
8g.41933459G>CCA371064694KAT6Ac.4761C>G (p.Cys1587Trp)
c.4767C>G (p.Cys1589Trp)
c.3442C>G
c.4893C>G (p.Cys1631Trp)
c.4872C>G (p.Cys1624Trp)
c.4779C>G (p.Cys1593Trp)
c.3333C>G (p.Cys1111Trp)
8g.41933459G=CA1779195946KAT6Ac.4761C= (p.Cys1587=)
c.4767C= (p.Cys1589=)
c.3442C=
c.4893C= (p.Cys1631=)
c.4872C= (p.Cys1624=)
c.4779C= (p.Cys1593=)
c.3333C= (p.Cys1111=)
8g.41933459G>TCA371064695KAT6Ac.4761C>A (p.Cys1587Ter)
c.4767C>A (p.Cys1589Ter)
c.3442C>A
c.4893C>A (p.Cys1631Ter)
c.4872C>A (p.Cys1624Ter)
c.4779C>A (p.Cys1593Ter)
c.3333C>A (p.Cys1111Ter)
dbSNP gnomAD v2
8g.41933460C>ACA371064696KAT6Ac.4760G>T (p.Cys1587Phe)
c.4766G>T (p.Cys1589Phe)
c.3441G>T
c.4892G>T (p.Cys1631Phe)
c.4871G>T (p.Cys1624Phe)
c.4778G>T (p.Cys1593Phe)
c.3332G>T (p.Cys1111Phe)
8g.41933460C>GCA371064697KAT6Ac.4760G>C (p.Cys1587Ser)
c.4766G>C (p.Cys1589Ser)
c.3441G>C
c.4892G>C (p.Cys1631Ser)
c.4871G>C (p.Cys1624Ser)
c.4778G>C (p.Cys1593Ser)
c.3332G>C (p.Cys1111Ser)
8g.41933460C>TCA371064698KAT6Ac.4760G>A (p.Cys1587Tyr)
c.4766G>A (p.Cys1589Tyr)
c.3441G>A
c.4892G>A (p.Cys1631Tyr)
c.4871G>A (p.Cys1624Tyr)
c.4778G>A (p.Cys1593Tyr)
c.3332G>A (p.Cys1111Tyr)
8g.41933461A>CCA371064699KAT6Ac.4759T>G (p.Cys1587Gly)
c.4765T>G (p.Cys1589Gly)
c.3440T>G
c.4891T>G (p.Cys1631Gly)
c.4870T>G (p.Cys1624Gly)
c.4777T>G (p.Cys1593Gly)
c.3331T>G (p.Cys1111Gly)
ClinVar dbSNP
8g.41933461A>GCA371064700KAT6Ac.4759T>C (p.Cys1587Arg)
c.4765T>C (p.Cys1589Arg)
c.3440T>C
c.4891T>C (p.Cys1631Arg)
c.4870T>C (p.Cys1624Arg)
c.4777T>C (p.Cys1593Arg)
c.3331T>C (p.Cys1111Arg)
8g.41933461A>TCA371064701KAT6Ac.4759T>A (p.Cys1587Ser)
c.4765T>A (p.Cys1589Ser)
c.3440T>A
c.4891T>A (p.Cys1631Ser)
c.4870T>A (p.Cys1624Ser)
c.4777T>A (p.Cys1593Ser)
c.3331T>A (p.Cys1111Ser)
8g.41933462G>ACA460783801KAT6Ac.4758C>T (p.Ser1586=)
c.4764C>T (p.Ser1588=)
c.3439C>T
c.4890C>T (p.Ser1630=)
c.4869C>T (p.Ser1623=)
c.4776C>T (p.Ser1592=)
c.3330C>T (p.Ser1110=)
8g.41933462G>CCA371064702KAT6Ac.4758C>G (p.Ser1586Arg)
c.4764C>G (p.Ser1588Arg)
c.3439C>G
c.4890C>G (p.Ser1630Arg)
c.4869C>G (p.Ser1623Arg)
c.4776C>G (p.Ser1592Arg)
c.3330C>G (p.Ser1110Arg)
8g.41933462G>TCA371064703KAT6Ac.4758C>A (p.Ser1586Arg)
c.4764C>A (p.Ser1588Arg)
c.3439C>A
c.4890C>A (p.Ser1630Arg)
c.4869C>A (p.Ser1623Arg)
c.4776C>A (p.Ser1592Arg)
c.3330C>A (p.Ser1110Arg)
8g.41933463C>ACA371064705KAT6Ac.4757G>T (p.Ser1586Ile)
c.4763G>T (p.Ser1588Ile)
c.3438G>T
c.4889G>T (p.Ser1630Ile)
c.4868G>T (p.Ser1623Ile)
c.4775G>T (p.Ser1592Ile)
c.3329G>T (p.Ser1110Ile)
8g.41933463C=CA1779195947KAT6Ac.4757G= (p.Ser1586=)
c.4763G= (p.Ser1588=)
c.3438G=
c.4889G= (p.Ser1630=)
c.4868G= (p.Ser1623=)
c.4775G= (p.Ser1592=)
c.3329G= (p.Ser1110=)
8g.41933463C>GCA371064706KAT6Ac.4757G>C (p.Ser1586Thr)
c.4763G>C (p.Ser1588Thr)
c.3438G>C
c.4889G>C (p.Ser1630Thr)
c.4868G>C (p.Ser1623Thr)
c.4775G>C (p.Ser1592Thr)
c.3329G>C (p.Ser1110Thr)
gnomAD v4
8g.41933463C>TCA371064704KAT6Ac.4757G>A (p.Ser1586Asn)
c.4763G>A (p.Ser1588Asn)
c.3438G>A
c.4889G>A (p.Ser1630Asn)
c.4868G>A (p.Ser1623Asn)
c.4775G>A (p.Ser1592Asn)
c.3329G>A (p.Ser1110Asn)
dbSNP
8g.41933464T>ACA371064708KAT6Ac.4756A>T (p.Ser1586Cys)
c.4762A>T (p.Ser1588Cys)
c.3437A>T
c.4888A>T (p.Ser1630Cys)
c.4867A>T (p.Ser1623Cys)
c.4774A>T (p.Ser1592Cys)
c.3328A>T (p.Ser1110Cys)
8g.41933464T>CCA371064707KAT6Ac.4756A>G (p.Ser1586Gly)
c.4762A>G (p.Ser1588Gly)
c.3437A>G
c.4888A>G (p.Ser1630Gly)
c.4867A>G (p.Ser1623Gly)
c.4774A>G (p.Ser1592Gly)
c.3328A>G (p.Ser1110Gly)
dbSNP gnomAD v3 gnomAD v4
8g.41933464T>GCA371064709KAT6Ac.4756A>C (p.Ser1586Arg)
c.4762A>C (p.Ser1588Arg)
c.3437A>C
c.4888A>C (p.Ser1630Arg)
c.4867A>C (p.Ser1623Arg)
c.4774A>C (p.Ser1592Arg)
c.3328A>C (p.Ser1110Arg)
8g.41933464T=CA1779195948KAT6Ac.4756A= (p.Ser1586=)
c.4762A= (p.Ser1588=)
c.3437A=
c.4888A= (p.Ser1630=)
c.4867A= (p.Ser1623=)
c.4774A= (p.Ser1592=)
c.3328A= (p.Ser1110=)
8g.41933465G>ACA460783806KAT6Ac.4755C>T (p.Ser1585=)
c.4761C>T (p.Ser1587=)
c.3436C>T
c.4887C>T (p.Ser1629=)
c.4866C>T (p.Ser1622=)
c.4773C>T (p.Ser1591=)
c.3327C>T (p.Ser1109=)
8g.41933465G>CCA371064710KAT6Ac.4755C>G (p.Ser1585Arg)
c.4761C>G (p.Ser1587Arg)
c.3436C>G
c.4887C>G (p.Ser1629Arg)
c.4866C>G (p.Ser1622Arg)
c.4773C>G (p.Ser1591Arg)
c.3327C>G (p.Ser1109Arg)
8g.41933465G>TCA371064711KAT6Ac.4755C>A (p.Ser1585Arg)
c.4761C>A (p.Ser1587Arg)
c.3436C>A
c.4887C>A (p.Ser1629Arg)
c.4866C>A (p.Ser1622Arg)
c.4773C>A (p.Ser1591Arg)
c.3327C>A (p.Ser1109Arg)
8g.41933466C>ACA371064712KAT6Ac.4754G>T (p.Ser1585Ile)
c.4760G>T (p.Ser1587Ile)
c.3435G>T
c.4886G>T (p.Ser1629Ile)
c.4865G>T (p.Ser1622Ile)
c.4772G>T (p.Ser1591Ile)
c.3326G>T (p.Ser1109Ile)
COSMIC
8g.41933466C=CA1779195949KAT6Ac.4754G= (p.Ser1585=)
c.4760G= (p.Ser1587=)
c.3435G=
c.4886G= (p.Ser1629=)
c.4865G= (p.Ser1622=)
c.4772G= (p.Ser1591=)
c.3326G= (p.Ser1109=)
8g.41933466C>GCA371064714KAT6Ac.4754G>C (p.Ser1585Thr)
c.4760G>C (p.Ser1587Thr)
c.3435G>C
c.4886G>C (p.Ser1629Thr)
c.4865G>C (p.Ser1622Thr)
c.4772G>C (p.Ser1591Thr)
c.3326G>C (p.Ser1109Thr)
8g.41933466C>TCA371064713KAT6Ac.4754G>A (p.Ser1585Asn)
c.4760G>A (p.Ser1587Asn)
c.3435G>A
c.4886G>A (p.Ser1629Asn)
c.4865G>A (p.Ser1622Asn)
c.4772G>A (p.Ser1591Asn)
c.3326G>A (p.Ser1109Asn)
dbSNP gnomAD v4
8g.41933467T>ACA371064715KAT6Ac.4753A>T (p.Ser1585Cys)
c.4759A>T (p.Ser1587Cys)
c.3434A>T
c.4885A>T (p.Ser1629Cys)
c.4864A>T (p.Ser1622Cys)
c.4771A>T (p.Ser1591Cys)
c.3325A>T (p.Ser1109Cys)
8g.41933467T>CCA371064717KAT6Ac.4753A>G (p.Ser1585Gly)
c.4759A>G (p.Ser1587Gly)
c.3434A>G
c.4885A>G (p.Ser1629Gly)
c.4864A>G (p.Ser1622Gly)
c.4771A>G (p.Ser1591Gly)
c.3325A>G (p.Ser1109Gly)
ClinVar dbSNP
8g.41933467T>GCA371064716KAT6Ac.4753A>C (p.Ser1585Arg)
c.4759A>C (p.Ser1587Arg)
c.3434A>C
c.4885A>C (p.Ser1629Arg)
c.4864A>C (p.Ser1622Arg)
c.4771A>C (p.Ser1591Arg)
c.3325A>C (p.Ser1109Arg)
8g.41933467T=CA1779195950KAT6Ac.4753A= (p.Ser1585=)
c.4759A= (p.Ser1587=)
c.3434A=
c.4885A= (p.Ser1629=)
c.4864A= (p.Ser1622=)
c.4771A= (p.Ser1591=)
c.3325A= (p.Ser1109=)
8g.41933468C>ACA371064718KAT6Ac.4752G>T (p.Gln1584His)
c.4758G>T (p.Gln1586His)
c.3433G>T
c.4884G>T (p.Gln1628His)
c.4863G>T (p.Gln1621His)
c.4770G>T (p.Gln1590His)
c.3324G>T (p.Gln1108His)
8g.41933468C>GCA371064719KAT6Ac.4752G>C (p.Gln1584His)
c.4758G>C (p.Gln1586His)
c.3433G>C
c.4884G>C (p.Gln1628His)
c.4863G>C (p.Gln1621His)
c.4770G>C (p.Gln1590His)
c.3324G>C (p.Gln1108His)
ClinVar dbSNP
8g.41933468C>TCA460783811KAT6Ac.4752G>A (p.Gln1584=)
c.4758G>A (p.Gln1586=)
c.3433G>A
c.4884G>A (p.Gln1628=)
c.4863G>A (p.Gln1621=)
c.4770G>A (p.Gln1590=)
c.3324G>A (p.Gln1108=)
8g.41933469T>ACA371064720KAT6Ac.4751A>T (p.Gln1584Leu)
c.4757A>T (p.Gln1586Leu)
c.3432A>T
c.4883A>T (p.Gln1628Leu)
c.4862A>T (p.Gln1621Leu)
c.4769A>T (p.Gln1590Leu)
c.3323A>T (p.Gln1108Leu)
8g.41933469T>CCA371064722KAT6Ac.4751A>G (p.Gln1584Arg)
c.4757A>G (p.Gln1586Arg)
c.3432A>G
c.4883A>G (p.Gln1628Arg)
c.4862A>G (p.Gln1621Arg)
c.4769A>G (p.Gln1590Arg)
c.3323A>G (p.Gln1108Arg)
8g.41933469T>GCA371064721KAT6Ac.4751A>C (p.Gln1584Pro)
c.4757A>C (p.Gln1586Pro)
c.3432A>C
c.4883A>C (p.Gln1628Pro)
c.4862A>C (p.Gln1621Pro)
c.4769A>C (p.Gln1590Pro)
c.3323A>C (p.Gln1108Pro)
8g.41933470G>ACA371064723KAT6Ac.4750C>T (p.Gln1584Ter)
c.4756C>T (p.Gln1586Ter)
c.3431C>T
c.4882C>T (p.Gln1628Ter)
c.4861C>T (p.Gln1621Ter)
c.4768C>T (p.Gln1590Ter)
c.3322C>T (p.Gln1108Ter)
8g.41933470G>CCA371064724KAT6Ac.4750C>G (p.Gln1584Glu)
c.4756C>G (p.Gln1586Glu)
c.3431C>G
c.4882C>G (p.Gln1628Glu)
c.4861C>G (p.Gln1621Glu)
c.4768C>G (p.Gln1590Glu)
c.3322C>G (p.Gln1108Glu)
8g.41933470G>TCA371064725KAT6Ac.4750C>A (p.Gln1584Lys)
c.4756C>A (p.Gln1586Lys)
c.3431C>A
c.4882C>A (p.Gln1628Lys)
c.4861C>A (p.Gln1621Lys)
c.4768C>A (p.Gln1590Lys)
c.3322C>A (p.Gln1108Lys)
8g.41933471G>ACA460783815KAT6Ac.4749C>T (p.Ser1583=)
c.4755C>T (p.Ser1585=)
c.3430C>T
c.4881C>T (p.Ser1627=)
c.4860C>T (p.Ser1620=)
c.4767C>T (p.Ser1589=)
c.3321C>T (p.Ser1107=)
gnomAD v4
8g.41933471G>CCA460783816KAT6Ac.4749C>G (p.Ser1583=)
c.4755C>G (p.Ser1585=)
c.3430C>G
c.4881C>G (p.Ser1627=)
c.4860C>G (p.Ser1620=)
c.4767C>G (p.Ser1589=)
c.3321C>G (p.Ser1107=)
8g.41933471G>TCA460783817KAT6Ac.4749C>A (p.Ser1583=)
c.4755C>A (p.Ser1585=)
c.3430C>A
c.4881C>A (p.Ser1627=)
c.4860C>A (p.Ser1620=)
c.4767C>A (p.Ser1589=)
c.3321C>A (p.Ser1107=)
gnomAD v4
8g.41933472G>ACA371064726KAT6Ac.4748C>T (p.Ser1583Phe)
c.4754C>T (p.Ser1585Phe)
c.3429C>T
c.4880C>T (p.Ser1627Phe)
c.4859C>T (p.Ser1620Phe)
c.4766C>T (p.Ser1589Phe)
c.3320C>T (p.Ser1107Phe)
COSMIC
8g.41933472G>CCA371064727KAT6Ac.4748C>G (p.Ser1583Cys)
c.4754C>G (p.Ser1585Cys)
c.3429C>G
c.4880C>G (p.Ser1627Cys)
c.4859C>G (p.Ser1620Cys)
c.4766C>G (p.Ser1589Cys)
c.3320C>G (p.Ser1107Cys)
8g.41933472G>TCA371064728KAT6Ac.4748C>A (p.Ser1583Tyr)
c.4754C>A (p.Ser1585Tyr)
c.3429C>A
c.4880C>A (p.Ser1627Tyr)
c.4859C>A (p.Ser1620Tyr)
c.4766C>A (p.Ser1589Tyr)
c.3320C>A (p.Ser1107Tyr)
8g.41933473A=CA1779195951KAT6Ac.4747T= (p.Ser1583=)
c.4753T= (p.Ser1585=)
c.3428T=
c.4879T= (p.Ser1627=)
c.4858T= (p.Ser1620=)
c.4765T= (p.Ser1589=)
c.3319T= (p.Ser1107=)
8g.41933473A>CCA371064729KAT6Ac.4747T>G (p.Ser1583Ala)
c.4753T>G (p.Ser1585Ala)
c.3428T>G
c.4879T>G (p.Ser1627Ala)
c.4858T>G (p.Ser1620Ala)
c.4765T>G (p.Ser1589Ala)
c.3319T>G (p.Ser1107Ala)
8g.41933473A>GCA371064730KAT6Ac.4747T>C (p.Ser1583Pro)
c.4753T>C (p.Ser1585Pro)
c.3428T>C
c.4879T>C (p.Ser1627Pro)
c.4858T>C (p.Ser1620Pro)
c.4765T>C (p.Ser1589Pro)
c.3319T>C (p.Ser1107Pro)
dbSNP
8g.41933473A>TCA371064731KAT6Ac.4747T>A (p.Ser1583Thr)
c.4753T>A (p.Ser1585Thr)
c.3428T>A
c.4879T>A (p.Ser1627Thr)
c.4858T>A (p.Ser1620Thr)
c.4765T>A (p.Ser1589Thr)
c.3319T>A (p.Ser1107Thr)
8g.41933474A=CA1779195952KAT6Ac.4746T= (p.Ser1582=)
c.4752T= (p.Ser1584=)
c.3427T=
c.4878T= (p.Ser1626=)
c.4857T= (p.Ser1619=)
c.4764T= (p.Ser1588=)
c.3318T= (p.Ser1106=)
8g.41933474A>CCA460783826KAT6Ac.4746T>G (p.Ser1582=)
c.4752T>G (p.Ser1584=)
c.3427T>G
c.4878T>G (p.Ser1626=)
c.4857T>G (p.Ser1619=)
c.4764T>G (p.Ser1588=)
c.3318T>G (p.Ser1106=)
ClinVar dbSNP gnomAD v4
8g.41933474A>GCA460783827KAT6Ac.4746T>C (p.Ser1582=)
c.4752T>C (p.Ser1584=)
c.3427T>C
c.4878T>C (p.Ser1626=)
c.4857T>C (p.Ser1619=)
c.4764T>C (p.Ser1588=)
c.3318T>C (p.Ser1106=)
dbSNP gnomAD v2 gnomAD v4
8g.41933474A>TCA460783828KAT6Ac.4746T>A (p.Ser1582=)
c.4752T>A (p.Ser1584=)
c.3427T>A
c.4878T>A (p.Ser1626=)
c.4857T>A (p.Ser1619=)
c.4764T>A (p.Ser1588=)
c.3318T>A (p.Ser1106=)
8g.41933475G>ACA371064734KAT6Ac.4745C>T (p.Ser1582Phe)
c.4751C>T (p.Ser1584Phe)
c.3426C>T
c.4877C>T (p.Ser1626Phe)
c.4856C>T (p.Ser1619Phe)
c.4763C>T (p.Ser1588Phe)
c.3317C>T (p.Ser1106Phe)
dbSNP gnomAD v3 gnomAD v4
8g.41933475G>CCA371064733KAT6Ac.4745C>G (p.Ser1582Cys)
c.4751C>G (p.Ser1584Cys)
c.3426C>G
c.4877C>G (p.Ser1626Cys)
c.4856C>G (p.Ser1619Cys)
c.4763C>G (p.Ser1588Cys)
c.3317C>G (p.Ser1106Cys)
gnomAD v4
8g.41933475G=CA1779195953KAT6Ac.4745C= (p.Ser1582=)
c.4751C= (p.Ser1584=)
c.3426C=
c.4877C= (p.Ser1626=)
c.4856C= (p.Ser1619=)
c.4763C= (p.Ser1588=)
c.3317C= (p.Ser1106=)
8g.41933475G>TCA371064732KAT6Ac.4745C>A (p.Ser1582Tyr)
c.4751C>A (p.Ser1584Tyr)
c.3426C>A
c.4877C>A (p.Ser1626Tyr)
c.4856C>A (p.Ser1619Tyr)
c.4763C>A (p.Ser1588Tyr)
c.3317C>A (p.Ser1106Tyr)
8g.41933476A>CCA371064735KAT6Ac.4744T>G (p.Ser1582Ala)
c.4750T>G (p.Ser1584Ala)
c.3425T>G
c.4876T>G (p.Ser1626Ala)
c.4855T>G (p.Ser1619Ala)
c.4762T>G (p.Ser1588Ala)
c.3316T>G (p.Ser1106Ala)
8g.41933476A>GCA371064736KAT6Ac.4744T>C (p.Ser1582Pro)
c.4750T>C (p.Ser1584Pro)
c.3425T>C
c.4876T>C (p.Ser1626Pro)
c.4855T>C (p.Ser1619Pro)
c.4762T>C (p.Ser1588Pro)
c.3316T>C (p.Ser1106Pro)
8g.41933476A>TCA371064737KAT6Ac.4744T>A (p.Ser1582Thr)
c.4750T>A (p.Ser1584Thr)
c.3425T>A
c.4876T>A (p.Ser1626Thr)
c.4855T>A (p.Ser1619Thr)
c.4762T>A (p.Ser1588Thr)
c.3316T>A (p.Ser1106Thr)
8g.41933477G>ACA460783832KAT6Ac.4743C>T (p.Ser1581=)
c.4749C>T (p.Ser1583=)
c.3424C>T
c.4875C>T (p.Ser1625=)
c.4854C>T (p.Ser1618=)
c.4761C>T (p.Ser1587=)
c.3315C>T (p.Ser1105=)
gnomAD v4
8g.41933477G>CCA371064738KAT6Ac.4743C>G (p.Ser1581Arg)
c.4749C>G (p.Ser1583Arg)
c.3424C>G
c.4875C>G (p.Ser1625Arg)
c.4854C>G (p.Ser1618Arg)
c.4761C>G (p.Ser1587Arg)
c.3315C>G (p.Ser1105Arg)
8g.41933477G>TCA371064739KAT6Ac.4743C>A (p.Ser1581Arg)
c.4749C>A (p.Ser1583Arg)
c.3424C>A
c.4875C>A (p.Ser1625Arg)
c.4854C>A (p.Ser1618Arg)
c.4761C>A (p.Ser1587Arg)
c.3315C>A (p.Ser1105Arg)
8g.41933478C>ACA371064740KAT6Ac.4742G>T (p.Ser1581Ile)
c.4748G>T (p.Ser1583Ile)
c.3423G>T
c.4874G>T (p.Ser1625Ile)
c.4853G>T (p.Ser1618Ile)
c.4760G>T (p.Ser1587Ile)
c.3314G>T (p.Ser1105Ile)
8g.41933478C=CA1779195954KAT6Ac.4742G= (p.Ser1581=)
c.4748G= (p.Ser1583=)
c.3423G=
c.4874G= (p.Ser1625=)
c.4853G= (p.Ser1618=)
c.4760G= (p.Ser1587=)
c.3314G= (p.Ser1105=)
8g.41933478C>GCA371064741KAT6Ac.4742G>C (p.Ser1581Thr)
c.4748G>C (p.Ser1583Thr)
c.3423G>C
c.4874G>C (p.Ser1625Thr)
c.4853G>C (p.Ser1618Thr)
c.4760G>C (p.Ser1587Thr)
c.3314G>C (p.Ser1105Thr)
ClinVar
8g.41933478C>TCA371064742KAT6Ac.4742G>A (p.Ser1581Asn)
c.4748G>A (p.Ser1583Asn)
c.3423G>A
c.4874G>A (p.Ser1625Asn)
c.4853G>A (p.Ser1618Asn)
c.4760G>A (p.Ser1587Asn)
c.3314G>A (p.Ser1105Asn)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
8g.41933479T>ACA371064743KAT6Ac.4741A>T (p.Ser1581Cys)
c.4747A>T (p.Ser1583Cys)
c.3422A>T
c.4873A>T (p.Ser1625Cys)
c.4852A>T (p.Ser1618Cys)
c.4759A>T (p.Ser1587Cys)
c.3313A>T (p.Ser1105Cys)
8g.41933479T>CCA371064744KAT6Ac.4741A>G (p.Ser1581Gly)
c.4747A>G (p.Ser1583Gly)
c.3422A>G
c.4873A>G (p.Ser1625Gly)
c.4852A>G (p.Ser1618Gly)
c.4759A>G (p.Ser1587Gly)
c.3313A>G (p.Ser1105Gly)
8g.41933479T>GCA371064745KAT6Ac.4741A>C (p.Ser1581Arg)
c.4747A>C (p.Ser1583Arg)
c.3422A>C
c.4873A>C (p.Ser1625Arg)
c.4852A>C (p.Ser1618Arg)
c.4759A>C (p.Ser1587Arg)
c.3313A>C (p.Ser1105Arg)
gnomAD v4
8g.41933480G>ACA4729435KAT6Ac.4740C>T (p.Asn1580=)
c.4746C>T (p.Asn1582=)
c.3421C>T
c.4872C>T (p.Asn1624=)
c.4851C>T (p.Asn1617=)
c.4758C>T (p.Asn1586=)
c.3312C>T (p.Asn1104=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.41933480G>CCA371064747KAT6Ac.4740C>G (p.Asn1580Lys)
c.4746C>G (p.Asn1582Lys)
c.3421C>G
c.4872C>G (p.Asn1624Lys)
c.4851C>G (p.Asn1617Lys)
c.4758C>G (p.Asn1586Lys)
c.3312C>G (p.Asn1104Lys)
8g.41933480G=CA1779195955KAT6Ac.4740C= (p.Asn1580=)
c.4746C= (p.Asn1582=)
c.3421C=
c.4872C= (p.Asn1624=)
c.4851C= (p.Asn1617=)
c.4758C= (p.Asn1586=)
c.3312C= (p.Asn1104=)
8g.41933480G>TCA371064746KAT6Ac.4740C>A (p.Asn1580Lys)
c.4746C>A (p.Asn1582Lys)
c.3421C>A
c.4872C>A (p.Asn1624Lys)
c.4851C>A (p.Asn1617Lys)
c.4758C>A (p.Asn1586Lys)
c.3312C>A (p.Asn1104Lys)
8g.41933481T>ACA371064748KAT6Ac.4739A>T (p.Asn1580Ile)
c.4745A>T (p.Asn1582Ile)
c.3420A>T
c.4871A>T (p.Asn1624Ile)
c.4850A>T (p.Asn1617Ile)
c.4757A>T (p.Asn1586Ile)
c.3311A>T (p.Asn1104Ile)
8g.41933481T>CCA371064749KAT6Ac.4739A>G (p.Asn1580Ser)
c.4745A>G (p.Asn1582Ser)
c.3420A>G
c.4871A>G (p.Asn1624Ser)
c.4850A>G (p.Asn1617Ser)
c.4757A>G (p.Asn1586Ser)
c.3311A>G (p.Asn1104Ser)
8g.41933481T>GCA371064750KAT6Ac.4739A>C (p.Asn1580Thr)
c.4745A>C (p.Asn1582Thr)
c.3420A>C
c.4871A>C (p.Asn1624Thr)
c.4850A>C (p.Asn1617Thr)
c.4757A>C (p.Asn1586Thr)
c.3311A>C (p.Asn1104Thr)
8g.41933482T>ACA371064751KAT6Ac.4738A>T (p.Asn1580Tyr)
c.4744A>T (p.Asn1582Tyr)
c.3419A>T
c.4870A>T (p.Asn1624Tyr)
c.4849A>T (p.Asn1617Tyr)
c.4756A>T (p.Asn1586Tyr)
c.3310A>T (p.Asn1104Tyr)
8g.41933482T>CCA371064752KAT6Ac.4738A>G (p.Asn1580Asp)
c.4744A>G (p.Asn1582Asp)
c.3419A>G
c.4870A>G (p.Asn1624Asp)
c.4849A>G (p.Asn1617Asp)
c.4756A>G (p.Asn1586Asp)
c.3310A>G (p.Asn1104Asp)
8g.41933482T>GCA371064753KAT6Ac.4738A>C (p.Asn1580His)
c.4744A>C (p.Asn1582His)
c.3419A>C
c.4870A>C (p.Asn1624His)
c.4849A>C (p.Asn1617His)
c.4756A>C (p.Asn1586His)
c.3310A>C (p.Asn1104His)
8g.41933483C>ACA460783840KAT6Ac.4737G>T (p.Gly1579=)
c.4743G>T (p.Gly1581=)
c.3418G>T
c.4869G>T (p.Gly1623=)
c.4848G>T (p.Gly1616=)
c.4755G>T (p.Gly1585=)
c.3309G>T (p.Gly1103=)
gnomAD v4
8g.41933483C=CA1779195956KAT6Ac.4737G= (p.Gly1579=)
c.4743G= (p.Gly1581=)
c.3418G=
c.4869G= (p.Gly1623=)
c.4848G= (p.Gly1616=)
c.4755G= (p.Gly1585=)
c.3309G= (p.Gly1103=)
8g.41933483C>GCA175939173KAT6Ac.4737G>C (p.Gly1579=)
c.4743G>C (p.Gly1581=)
c.3418G>C
c.4869G>C (p.Gly1623=)
c.4848G>C (p.Gly1616=)
c.4755G>C (p.Gly1585=)
c.3309G>C (p.Gly1103=)
dbSNP gnomAD v4
8g.41933483C>TCA460783842KAT6Ac.4737G>A (p.Gly1579=)
c.4743G>A (p.Gly1581=)
c.3418G>A
c.4869G>A (p.Gly1623=)
c.4848G>A (p.Gly1616=)
c.4755G>A (p.Gly1585=)
c.3309G>A (p.Gly1103=)
dbSNP gnomAD v2 gnomAD v4
8g.41933484C>ACA371064754KAT6Ac.4736G>T (p.Gly1579Val)
c.4742G>T (p.Gly1581Val)
c.3417G>T
c.4868G>T (p.Gly1623Val)
c.4847G>T (p.Gly1616Val)
c.4754G>T (p.Gly1585Val)
c.3308G>T (p.Gly1103Val)
8g.41933484C>GCA371064755KAT6Ac.4736G>C (p.Gly1579Ala)
c.4742G>C (p.Gly1581Ala)
c.3417G>C
c.4868G>C (p.Gly1623Ala)
c.4847G>C (p.Gly1616Ala)
c.4754G>C (p.Gly1585Ala)
c.3308G>C (p.Gly1103Ala)
8g.41933484C>TCA371064756KAT6Ac.4736G>A (p.Gly1579Glu)
c.4742G>A (p.Gly1581Glu)
c.3417G>A
c.4868G>A (p.Gly1623Glu)
c.4847G>A (p.Gly1616Glu)
c.4754G>A (p.Gly1585Glu)
c.3308G>A (p.Gly1103Glu)
gnomAD v4 COSMIC
8g.41933485C>ACA371064757KAT6Ac.4735G>T (p.Gly1579Trp)
c.4741G>T (p.Gly1581Trp)
c.3416G>T
c.4867G>T (p.Gly1623Trp)
c.4846G>T (p.Gly1616Trp)
c.4753G>T (p.Gly1585Trp)
c.3307G>T (p.Gly1103Trp)
8g.41933485C>GCA371064758KAT6Ac.4735G>C (p.Gly1579Arg)
c.4741G>C (p.Gly1581Arg)
c.3416G>C
c.4867G>C (p.Gly1623Arg)
c.4846G>C (p.Gly1616Arg)
c.4753G>C (p.Gly1585Arg)
c.3307G>C (p.Gly1103Arg)
8g.41933485C>TCA371064759KAT6Ac.4735G>A (p.Gly1579Arg)
c.4741G>A (p.Gly1581Arg)
c.3416G>A
c.4867G>A (p.Gly1623Arg)
c.4846G>A (p.Gly1616Arg)
c.4753G>A (p.Gly1585Arg)
c.3307G>A (p.Gly1103Arg)
8g.41933486A>CCA371064761KAT6Ac.4734T>G (p.Cys1578Trp)
c.4740T>G (p.Cys1580Trp)
c.3415T>G
c.4866T>G (p.Cys1622Trp)
c.4845T>G (p.Cys1615Trp)
c.4752T>G (p.Cys1584Trp)
c.3306T>G (p.Cys1102Trp)
8g.41933486A>GCA460783845KAT6Ac.4734T>C (p.Cys1578=)
c.4740T>C (p.Cys1580=)
c.3415T>C
c.4866T>C (p.Cys1622=)
c.4845T>C (p.Cys1615=)
c.4752T>C (p.Cys1584=)
c.3306T>C (p.Cys1102=)
8g.41933486A>TCA371064760KAT6Ac.4734T>A (p.Cys1578Ter)
c.4740T>A (p.Cys1580Ter)
c.3415T>A
c.4866T>A (p.Cys1622Ter)
c.4845T>A (p.Cys1615Ter)
c.4752T>A (p.Cys1584Ter)
c.3306T>A (p.Cys1102Ter)
8g.41933487C>ACA371064762KAT6Ac.4733G>T (p.Cys1578Phe)
c.4739G>T (p.Cys1580Phe)
c.3414G>T
c.4865G>T (p.Cys1622Phe)
c.4844G>T (p.Cys1615Phe)
c.4751G>T (p.Cys1584Phe)
c.3305G>T (p.Cys1102Phe)
8g.41933487C>GCA371064763KAT6Ac.4733G>C (p.Cys1578Ser)
c.4739G>C (p.Cys1580Ser)
c.3414G>C
c.4865G>C (p.Cys1622Ser)
c.4844G>C (p.Cys1615Ser)
c.4751G>C (p.Cys1584Ser)
c.3305G>C (p.Cys1102Ser)
8g.41933487C>TCA371064764KAT6Ac.4733G>A (p.Cys1578Tyr)
c.4739G>A (p.Cys1580Tyr)
c.3414G>A
c.4865G>A (p.Cys1622Tyr)
c.4844G>A (p.Cys1615Tyr)
c.4751G>A (p.Cys1584Tyr)
c.3305G>A (p.Cys1102Tyr)
8g.41933488A>CCA371064765KAT6Ac.4732T>G (p.Cys1578Gly)
c.4738T>G (p.Cys1580Gly)
c.3413T>G
c.4864T>G (p.Cys1622Gly)
c.4843T>G (p.Cys1615Gly)
c.4750T>G (p.Cys1584Gly)
c.3304T>G (p.Cys1102Gly)
8g.41933488A>GCA371064766KAT6Ac.4732T>C (p.Cys1578Arg)
c.4738T>C (p.Cys1580Arg)
c.3413T>C
c.4864T>C (p.Cys1622Arg)
c.4843T>C (p.Cys1615Arg)
c.4750T>C (p.Cys1584Arg)
c.3304T>C (p.Cys1102Arg)
8g.41933488A>TCA371064767KAT6Ac.4732T>A (p.Cys1578Ser)
c.4738T>A (p.Cys1580Ser)
c.3413T>A
c.4864T>A (p.Cys1622Ser)
c.4843T>A (p.Cys1615Ser)
c.4750T>A (p.Cys1584Ser)
c.3304T>A (p.Cys1102Ser)
8g.41933489G>ACA460783849KAT6Ac.4731C>T (p.Ile1577=)
c.4737C>T (p.Ile1579=)
c.3412C>T
c.4863C>T (p.Ile1621=)
c.4842C>T (p.Ile1614=)
c.4749C>T (p.Ile1583=)
c.3303C>T (p.Ile1101=)
8g.41933489G>CCA371064768KAT6Ac.4731C>G (p.Ile1577Met)
c.4737C>G (p.Ile1579Met)
c.3412C>G
c.4863C>G (p.Ile1621Met)
c.4842C>G (p.Ile1614Met)
c.4749C>G (p.Ile1583Met)
c.3303C>G (p.Ile1101Met)
8g.41933489G>TCA460783850KAT6Ac.4731C>A (p.Ile1577=)
c.4737C>A (p.Ile1579=)
c.3412C>A
c.4863C>A (p.Ile1621=)
c.4842C>A (p.Ile1614=)
c.4749C>A (p.Ile1583=)
c.3303C>A (p.Ile1101=)
8g.41933490A>CCA371064769KAT6Ac.4730T>G (p.Ile1577Ser)
c.4736T>G (p.Ile1579Ser)
c.3411T>G
c.4862T>G (p.Ile1621Ser)
c.4841T>G (p.Ile1614Ser)
c.4748T>G (p.Ile1583Ser)
c.3302T>G (p.Ile1101Ser)
8g.41933490A>GCA371064770KAT6Ac.4730T>C (p.Ile1577Thr)
c.4736T>C (p.Ile1579Thr)
c.3411T>C
c.4862T>C (p.Ile1621Thr)
c.4841T>C (p.Ile1614Thr)
c.4748T>C (p.Ile1583Thr)
c.3302T>C (p.Ile1101Thr)
8g.41933490A>TCA371064771KAT6Ac.4730T>A (p.Ile1577Asn)
c.4736T>A (p.Ile1579Asn)
c.3411T>A
c.4862T>A (p.Ile1621Asn)
c.4841T>A (p.Ile1614Asn)
c.4748T>A (p.Ile1583Asn)
c.3302T>A (p.Ile1101Asn)
8g.41933491T>ACA371064772KAT6Ac.4729A>T (p.Ile1577Phe)
c.4735A>T (p.Ile1579Phe)
c.3410A>T
c.4861A>T (p.Ile1621Phe)
c.4840A>T (p.Ile1614Phe)
c.4747A>T (p.Ile1583Phe)
c.3301A>T (p.Ile1101Phe)
8g.41933491T>CCA371064773KAT6Ac.4729A>G (p.Ile1577Val)
c.4735A>G (p.Ile1579Val)
c.3410A>G
c.4861A>G (p.Ile1621Val)
c.4840A>G (p.Ile1614Val)
c.4747A>G (p.Ile1583Val)
c.3301A>G (p.Ile1101Val)
dbSNP gnomAD v4
8g.41933491T>GCA371064774KAT6Ac.4729A>C (p.Ile1577Leu)
c.4735A>C (p.Ile1579Leu)
c.3410A>C
c.4861A>C (p.Ile1621Leu)
c.4840A>C (p.Ile1614Leu)
c.4747A>C (p.Ile1583Leu)
c.3301A>C (p.Ile1101Leu)
8g.41933491T=CA1779195957KAT6Ac.4729A= (p.Ile1577=)
c.4735A= (p.Ile1579=)
c.3410A=
c.4861A= (p.Ile1621=)
c.4840A= (p.Ile1614=)
c.4747A= (p.Ile1583=)
c.3301A= (p.Ile1101=)
8g.41933492G>ACA460783853KAT6Ac.4728C>T (p.Ser1576=)
c.4734C>T (p.Ser1578=)
c.3409C>T
c.4860C>T (p.Ser1620=)
c.4839C>T (p.Ser1613=)
c.4746C>T (p.Ser1582=)
c.3300C>T (p.Ser1100=)
8g.41933492G>CCA371064776KAT6Ac.4728C>G (p.Ser1576Arg)
c.4734C>G (p.Ser1578Arg)
c.3409C>G
c.4860C>G (p.Ser1620Arg)
c.4839C>G (p.Ser1613Arg)
c.4746C>G (p.Ser1582Arg)
c.3300C>G (p.Ser1100Arg)
8g.41933492G>TCA371064775KAT6Ac.4728C>A (p.Ser1576Arg)
c.4734C>A (p.Ser1578Arg)
c.3409C>A
c.4860C>A (p.Ser1620Arg)
c.4839C>A (p.Ser1613Arg)
c.4746C>A (p.Ser1582Arg)
c.3300C>A (p.Ser1100Arg)
8g.41933493C>ACA371064777KAT6Ac.4727G>T (p.Ser1576Ile)
c.4733G>T (p.Ser1578Ile)
c.3408G>T
c.4859G>T (p.Ser1620Ile)
c.4838G>T (p.Ser1613Ile)
c.4745G>T (p.Ser1582Ile)
c.3299G>T (p.Ser1100Ile)
8g.41933493C=CA1779195958KAT6Ac.4727G= (p.Ser1576=)
c.4733G= (p.Ser1578=)
c.3408G=
c.4859G= (p.Ser1620=)
c.4838G= (p.Ser1613=)
c.4745G= (p.Ser1582=)
c.3299G= (p.Ser1100=)
8g.41933493C>GCA371064779KAT6Ac.4727G>C (p.Ser1576Thr)
c.4733G>C (p.Ser1578Thr)
c.3408G>C
c.4859G>C (p.Ser1620Thr)
c.4838G>C (p.Ser1613Thr)
c.4745G>C (p.Ser1582Thr)
c.3299G>C (p.Ser1100Thr)
8g.41933493C>TCA371064778KAT6Ac.4727G>A (p.Ser1576Asn)
c.4733G>A (p.Ser1578Asn)
c.3408G>A
c.4859G>A (p.Ser1620Asn)
c.4838G>A (p.Ser1613Asn)
c.4745G>A (p.Ser1582Asn)
c.3299G>A (p.Ser1100Asn)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.41933494T>ACA371064780KAT6Ac.4726A>T (p.Ser1576Cys)
c.4732A>T (p.Ser1578Cys)
c.3407A>T
c.4858A>T (p.Ser1620Cys)
c.4837A>T (p.Ser1613Cys)
c.4744A>T (p.Ser1582Cys)
c.3298A>T (p.Ser1100Cys)
8g.41933494T>CCA371064781KAT6Ac.4726A>G (p.Ser1576Gly)
c.4732A>G (p.Ser1578Gly)
c.3407A>G
c.4858A>G (p.Ser1620Gly)
c.4837A>G (p.Ser1613Gly)
c.4744A>G (p.Ser1582Gly)
c.3298A>G (p.Ser1100Gly)
gnomAD v4
8g.41933494T>GCA371064782KAT6Ac.4726A>C (p.Ser1576Arg)
c.4732A>C (p.Ser1578Arg)
c.3407A>C
c.4858A>C (p.Ser1620Arg)
c.4837A>C (p.Ser1613Arg)
c.4744A>C (p.Ser1582Arg)
c.3298A>C (p.Ser1100Arg)
8g.41933495G>ACA460783858KAT6Ac.4725C>T (p.Gly1575=)
c.4731C>T (p.Gly1577=)
c.3406C>T
c.4857C>T (p.Gly1619=)
c.4836C>T (p.Gly1612=)
c.4743C>T (p.Gly1581=)
c.3297C>T (p.Gly1099=)
dbSNP gnomAD v2 gnomAD v4
8g.41933495G>CCA460783859KAT6Ac.4725C>G (p.Gly1575=)
c.4731C>G (p.Gly1577=)
c.3406C>G
c.4857C>G (p.Gly1619=)
c.4836C>G (p.Gly1612=)
c.4743C>G (p.Gly1581=)
c.3297C>G (p.Gly1099=)
8g.41933495G=CA1779195959KAT6Ac.4725C= (p.Gly1575=)
c.4731C= (p.Gly1577=)
c.3406C=
c.4857C= (p.Gly1619=)
c.4836C= (p.Gly1612=)
c.4743C= (p.Gly1581=)
c.3297C= (p.Gly1099=)
8g.41933495G>TCA460783860KAT6Ac.4725C>A (p.Gly1575=)
c.4731C>A (p.Gly1577=)
c.3406C>A
c.4857C>A (p.Gly1619=)
c.4836C>A (p.Gly1612=)
c.4743C>A (p.Gly1581=)
c.3297C>A (p.Gly1099=)
8g.41933496C>ACA371064783KAT6Ac.4724G>T (p.Gly1575Val)
c.4730G>T (p.Gly1577Val)
c.3405G>T
c.4856G>T (p.Gly1619Val)
c.4835G>T (p.Gly1612Val)
c.4742G>T (p.Gly1581Val)
c.3296G>T (p.Gly1099Val)
ClinVar
8g.41933496C>GCA371064784KAT6Ac.4724G>C (p.Gly1575Ala)
c.4730G>C (p.Gly1577Ala)
c.3405G>C
c.4856G>C (p.Gly1619Ala)
c.4835G>C (p.Gly1612Ala)
c.4742G>C (p.Gly1581Ala)
c.3296G>C (p.Gly1099Ala)
8g.41933496C>TCA371064785KAT6Ac.4724G>A (p.Gly1575Asp)
c.4730G>A (p.Gly1577Asp)
c.3405G>A
c.4856G>A (p.Gly1619Asp)
c.4835G>A (p.Gly1612Asp)
c.4742G>A (p.Gly1581Asp)
c.3296G>A (p.Gly1099Asp)
8g.41933497C>ACA371064786KAT6Ac.4723G>T (p.Gly1575Cys)
c.4729G>T (p.Gly1577Cys)
c.3404G>T
c.4855G>T (p.Gly1619Cys)
c.4834G>T (p.Gly1612Cys)
c.4741G>T (p.Gly1581Cys)
c.3295G>T (p.Gly1099Cys)
8g.41933497C=CA1779195960KAT6Ac.4723G= (p.Gly1575=)
c.4729G= (p.Gly1577=)
c.3404G=
c.4855G= (p.Gly1619=)
c.4834G= (p.Gly1612=)
c.4741G= (p.Gly1581=)
c.3295G= (p.Gly1099=)
8g.41933497C>GCA371064787KAT6Ac.4723G>C (p.Gly1575Arg)
c.4729G>C (p.Gly1577Arg)
c.3404G>C
c.4855G>C (p.Gly1619Arg)
c.4834G>C (p.Gly1612Arg)
c.4741G>C (p.Gly1581Arg)
c.3295G>C (p.Gly1099Arg)
8g.41933497C>TCA4729436KAT6Ac.4723G>A (p.Gly1575Ser)
c.4729G>A (p.Gly1577Ser)
c.3404G>A
c.4855G>A (p.Gly1619Ser)
c.4834G>A (p.Gly1612Ser)
c.4741G>A (p.Gly1581Ser)
c.3295G>A (p.Gly1099Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.41933498G>ACA4729437KAT6Ac.4722C>T (p.Gly1574=)
c.4728C>T (p.Gly1576=)
c.3403C>T
c.4854C>T (p.Gly1618=)
c.4833C>T (p.Gly1611=)
c.4740C>T (p.Gly1580=)
c.3294C>T (p.Gly1098=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.41933498G>CCA175939179KAT6Ac.4722C>G (p.Gly1574=)
c.4728C>G (p.Gly1576=)
c.3403C>G
c.4854C>G (p.Gly1618=)
c.4833C>G (p.Gly1611=)
c.4740C>G (p.Gly1580=)
c.3294C>G (p.Gly1098=)
dbSNP
8g.41933498G=CA1779195961KAT6Ac.4722C= (p.Gly1574=)
c.4728C= (p.Gly1576=)
c.3403C=
c.4854C= (p.Gly1618=)
c.4833C= (p.Gly1611=)
c.4740C= (p.Gly1580=)
c.3294C= (p.Gly1098=)
8g.41933498G>TCA460783861KAT6Ac.4722C>A (p.Gly1574=)
c.4728C>A (p.Gly1576=)
c.3403C>A
c.4854C>A (p.Gly1618=)
c.4833C>A (p.Gly1611=)
c.4740C>A (p.Gly1580=)
c.3294C>A (p.Gly1098=)
8g.41933499C>ACA371064788KAT6Ac.4721G>T (p.Gly1574Val)
c.4727G>T (p.Gly1576Val)
c.3402G>T
c.4853G>T (p.Gly1618Val)
c.4832G>T (p.Gly1611Val)
c.4739G>T (p.Gly1580Val)
c.3293G>T (p.Gly1098Val)
8g.41933499C>GCA371064789KAT6Ac.4721G>C (p.Gly1574Ala)
c.4727G>C (p.Gly1576Ala)
c.3402G>C
c.4853G>C (p.Gly1618Ala)
c.4832G>C (p.Gly1611Ala)
c.4739G>C (p.Gly1580Ala)
c.3293G>C (p.Gly1098Ala)
8g.41933499C>TCA371064791KAT6Ac.4721G>A (p.Gly1574Asp)
c.4727G>A (p.Gly1576Asp)
c.3402G>A
c.4853G>A (p.Gly1618Asp)
c.4832G>A (p.Gly1611Asp)
c.4739G>A (p.Gly1580Asp)
c.3293G>A (p.Gly1098Asp)
8g.41933500C>ACA371064792KAT6Ac.4720G>T (p.Gly1574Cys)
c.4726G>T (p.Gly1576Cys)
c.3401G>T
c.4852G>T (p.Gly1618Cys)
c.4831G>T (p.Gly1611Cys)
c.4738G>T (p.Gly1580Cys)
c.3292G>T (p.Gly1098Cys)
COSMIC
8g.41933500C=CA1779195962KAT6Ac.4720G= (p.Gly1574=)
c.4726G= (p.Gly1576=)
c.3401G=
c.4852G= (p.Gly1618=)
c.4831G= (p.Gly1611=)
c.4738G= (p.Gly1580=)
c.3292G= (p.Gly1098=)
8g.41933500C>GCA371064794KAT6Ac.4720G>C (p.Gly1574Arg)
c.4726G>C (p.Gly1576Arg)
c.3401G>C
c.4852G>C (p.Gly1618Arg)
c.4831G>C (p.Gly1611Arg)
c.4738G>C (p.Gly1580Arg)
c.3292G>C (p.Gly1098Arg)
8g.41933500C>TCA371064793KAT6Ac.4720G>A (p.Gly1574Ser)
c.4726G>A (p.Gly1576Ser)
c.3401G>A
c.4852G>A (p.Gly1618Ser)
c.4831G>A (p.Gly1611Ser)
c.4738G>A (p.Gly1580Ser)
c.3292G>A (p.Gly1098Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
8g.41933501C>ACA371064795KAT6Ac.4719G>T (p.Met1573Ile)
c.4725G>T (p.Met1575Ile)
c.3400G>T
c.4851G>T (p.Met1617Ile)
c.4830G>T (p.Met1610Ile)
c.4737G>T (p.Met1579Ile)
c.3291G>T (p.Met1097Ile)
8g.41933501C>GCA371064796KAT6Ac.4719G>C (p.Met1573Ile)
c.4725G>C (p.Met1575Ile)
c.3400G>C
c.4851G>C (p.Met1617Ile)
c.4830G>C (p.Met1610Ile)
c.4737G>C (p.Met1579Ile)
c.3291G>C (p.Met1097Ile)
gnomAD v4
8g.41933501C>TCA371064797KAT6Ac.4719G>A (p.Met1573Ile)
c.4725G>A (p.Met1575Ile)
c.3400G>A
c.4851G>A (p.Met1617Ile)
c.4830G>A (p.Met1610Ile)
c.4737G>A (p.Met1579Ile)
c.3291G>A (p.Met1097Ile)
8g.41933502A>CCA371064800KAT6Ac.4718T>G (p.Met1573Arg)
c.4724T>G (p.Met1575Arg)
c.3399T>G
c.4850T>G (p.Met1617Arg)
c.4829T>G (p.Met1610Arg)
c.4736T>G (p.Met1579Arg)
c.3290T>G (p.Met1097Arg)
gnomAD v3 gnomAD v4
8g.41933502A>GCA371064802KAT6Ac.4718T>C (p.Met1573Thr)
c.4724T>C (p.Met1575Thr)
c.3399T>C
c.4850T>C (p.Met1617Thr)
c.4829T>C (p.Met1610Thr)
c.4736T>C (p.Met1579Thr)
c.3290T>C (p.Met1097Thr)
gnomAD v4
8g.41933502A>TCA371064803KAT6Ac.4718T>A (p.Met1573Lys)
c.4724T>A (p.Met1575Lys)
c.3399T>A
c.4850T>A (p.Met1617Lys)
c.4829T>A (p.Met1610Lys)
c.4736T>A (p.Met1579Lys)
c.3290T>A (p.Met1097Lys)
8g.41933503T>ACA371064806KAT6Ac.4717A>T (p.Met1573Leu)
c.4723A>T (p.Met1575Leu)
c.3398A>T
c.4849A>T (p.Met1617Leu)
c.4828A>T (p.Met1610Leu)
c.4735A>T (p.Met1579Leu)
c.3289A>T (p.Met1097Leu)
8g.41933503T>CCA371064808KAT6Ac.4717A>G (p.Met1573Val)
c.4723A>G (p.Met1575Val)
c.3398A>G
c.4849A>G (p.Met1617Val)
c.4828A>G (p.Met1610Val)
c.4735A>G (p.Met1579Val)
c.3289A>G (p.Met1097Val)
8g.41933503T>GCA371064809KAT6Ac.4717A>C (p.Met1573Leu)
c.4723A>C (p.Met1575Leu)
c.3398A>C
c.4849A>C (p.Met1617Leu)
c.4828A>C (p.Met1610Leu)
c.4735A>C (p.Met1579Leu)
c.3289A>C (p.Met1097Leu)
8g.41933507_41933514delCA2687076957KAT6Ac.4710_4717del (p.Ser1571GlyfsTer?)
c.4716_4723del (p.Ser1573GlyfsTer?)
c.3391_3398del
c.4842_4849del (p.Ser1615GlyfsTer?)
c.4821_4828del (p.Ser1608GlyfsTer?)
c.4728_4735del (p.Ser1577GlyfsTer?)
c.3282_3289del (p.Ser1095GlyfsTer?)
gnomAD v4
8g.41933504C>ACA460783148KAT6Ac.4716G>T (p.Thr1572=)
c.4722G>T (p.Thr1574=)
c.3397G>T
c.4848G>T (p.Thr1616=)
c.4827G>T (p.Thr1609=)
c.4734G>T (p.Thr1578=)
c.3288G>T (p.Thr1096=)
8g.41933504C=CA1779195963KAT6Ac.4716G= (p.Thr1572=)
c.4722G= (p.Thr1574=)
c.3397G=
c.4848G= (p.Thr1616=)
c.4827G= (p.Thr1609=)
c.4734G= (p.Thr1578=)
c.3288G= (p.Thr1096=)
8g.41933504C>GCA460783149KAT6Ac.4716G>C (p.Thr1572=)
c.4722G>C (p.Thr1574=)
c.3397G>C
c.4848G>C (p.Thr1616=)
c.4827G>C (p.Thr1609=)
c.4734G>C (p.Thr1578=)
c.3288G>C (p.Thr1096=)
gnomAD v4
8g.41933504C>TCA460783150KAT6Ac.4716G>A (p.Thr1572=)
c.4722G>A (p.Thr1574=)
c.3397G>A
c.4848G>A (p.Thr1616=)
c.4827G>A (p.Thr1609=)
c.4734G>A (p.Thr1578=)
c.3288G>A (p.Thr1096=)
ClinVar dbSNP gnomAD v4
8g.41933505G>ACA4729438KAT6Ac.4715C>T (p.Thr1572Met)
c.4721C>T (p.Thr1574Met)
c.3396C>T
c.4847C>T (p.Thr1616Met)
c.4826C>T (p.Thr1609Met)
c.4733C>T (p.Thr1578Met)
c.3287C>T (p.Thr1096Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
8g.41933505G>CCA371064815KAT6Ac.4715C>G (p.Thr1572Arg)
c.4721C>G (p.Thr1574Arg)
c.3396C>G
c.4847C>G (p.Thr1616Arg)
c.4826C>G (p.Thr1609Arg)
c.4733C>G (p.Thr1578Arg)
c.3287C>G (p.Thr1096Arg)
8g.41933505G=CA1779195964KAT6Ac.4715C= (p.Thr1572=)
c.4721C= (p.Thr1574=)
c.3396C=
c.4847C= (p.Thr1616=)
c.4826C= (p.Thr1609=)
c.4733C= (p.Thr1578=)
c.3287C= (p.Thr1096=)
8g.41933505G>TCA371064812KAT6Ac.4715C>A (p.Thr1572Lys)
c.4721C>A (p.Thr1574Lys)
c.3396C>A
c.4847C>A (p.Thr1616Lys)
c.4826C>A (p.Thr1609Lys)
c.4733C>A (p.Thr1578Lys)
c.3287C>A (p.Thr1096Lys)
8g.41933506T>ACA371064817KAT6Ac.4714A>T (p.Thr1572Ser)
c.4720A>T (p.Thr1574Ser)
c.3395A>T
c.4846A>T (p.Thr1616Ser)
c.4825A>T (p.Thr1609Ser)
c.4732A>T (p.Thr1578Ser)
c.3286A>T (p.Thr1096Ser)
8g.41933506T>CCA371064819KAT6Ac.4714A>G (p.Thr1572Ala)
c.4720A>G (p.Thr1574Ala)
c.3395A>G
c.4846A>G (p.Thr1616Ala)
c.4825A>G (p.Thr1609Ala)
c.4732A>G (p.Thr1578Ala)
c.3286A>G (p.Thr1096Ala)
8g.41933506T>GCA371064821KAT6Ac.4714A>C (p.Thr1572Pro)
c.4720A>C (p.Thr1574Pro)
c.3395A>C
c.4846A>C (p.Thr1616Pro)
c.4825A>C (p.Thr1609Pro)
c.4732A>C (p.Thr1578Pro)
c.3286A>C (p.Thr1096Pro)
gnomAD v4
8g.41933507G>ACA460783155KAT6Ac.4713C>T (p.Ser1571=)
c.4719C>T (p.Ser1573=)
c.3394C>T
c.4845C>T (p.Ser1615=)
c.4824C>T (p.Ser1608=)
c.4731C>T (p.Ser1577=)
c.3285C>T (p.Ser1095=)
8g.41933507G>CCA460783156KAT6Ac.4713C>G (p.Ser1571=)
c.4719C>G (p.Ser1573=)
c.3394C>G
c.4845C>G (p.Ser1615=)
c.4824C>G (p.Ser1608=)
c.4731C>G (p.Ser1577=)
c.3285C>G (p.Ser1095=)
8g.41933507G>TCA460783157KAT6Ac.4713C>A (p.Ser1571=)
c.4719C>A (p.Ser1573=)
c.3394C>A
c.4845C>A (p.Ser1615=)
c.4824C>A (p.Ser1608=)
c.4731C>A (p.Ser1577=)
c.3285C>A (p.Ser1095=)
8g.41933508G>ACA371064824KAT6Ac.4712C>T (p.Ser1571Phe)
c.4718C>T (p.Ser1573Phe)
c.3393C>T
c.4844C>T (p.Ser1615Phe)
c.4823C>T (p.Ser1608Phe)
c.4730C>T (p.Ser1577Phe)
c.3284C>T (p.Ser1095Phe)
8g.41933508G>CCA371064826KAT6Ac.4712C>G (p.Ser1571Cys)
c.4718C>G (p.Ser1573Cys)
c.3393C>G
c.4844C>G (p.Ser1615Cys)
c.4823C>G (p.Ser1608Cys)
c.4730C>G (p.Ser1577Cys)
c.3284C>G (p.Ser1095Cys)
gnomAD v4
8g.41933508G>TCA371064828KAT6Ac.4712C>A (p.Ser1571Tyr)
c.4718C>A (p.Ser1573Tyr)
c.3393C>A
c.4844C>A (p.Ser1615Tyr)
c.4823C>A (p.Ser1608Tyr)
c.4730C>A (p.Ser1577Tyr)
c.3284C>A (p.Ser1095Tyr)
8g.41933509A>CCA371064838KAT6Ac.4711T>G (p.Ser1571Ala)
c.4717T>G (p.Ser1573Ala)
c.3392T>G
c.4843T>G (p.Ser1615Ala)
c.4822T>G (p.Ser1608Ala)
c.4729T>G (p.Ser1577Ala)
c.3283T>G (p.Ser1095Ala)
8g.41933509A>GCA371064834KAT6Ac.4711T>C (p.Ser1571Pro)
c.4717T>C (p.Ser1573Pro)
c.3392T>C
c.4843T>C (p.Ser1615Pro)
c.4822T>C (p.Ser1608Pro)
c.4729T>C (p.Ser1577Pro)
c.3283T>C (p.Ser1095Pro)
8g.41933509A>TCA371064836KAT6Ac.4711T>A (p.Ser1571Thr)
c.4717T>A (p.Ser1573Thr)
c.3392T>A
c.4843T>A (p.Ser1615Thr)
c.4822T>A (p.Ser1608Thr)
c.4729T>A (p.Ser1577Thr)
c.3283T>A (p.Ser1095Thr)
8g.41933510G>ACA460783161KAT6Ac.4710C>T (p.Asp1570=)
c.4716C>T (p.Asp1572=)
c.3391C>T
c.4842C>T (p.Asp1614=)
c.4821C>T (p.Asp1607=)
c.4728C>T (p.Asp1576=)
c.3282C>T (p.Asp1094=)
gnomAD v4
8g.41933510G>CCA371064842KAT6Ac.4710C>G (p.Asp1570Glu)
c.4716C>G (p.Asp1572Glu)
c.3391C>G
c.4842C>G (p.Asp1614Glu)
c.4821C>G (p.Asp1607Glu)
c.4728C>G (p.Asp1576Glu)
c.3282C>G (p.Asp1094Glu)
8g.41933510G>TCA371064843KAT6Ac.4710C>A (p.Asp1570Glu)
c.4716C>A (p.Asp1572Glu)
c.3391C>A
c.4842C>A (p.Asp1614Glu)
c.4821C>A (p.Asp1607Glu)
c.4728C>A (p.Asp1576Glu)
c.3282C>A (p.Asp1094Glu)
8g.41933511T>ACA371064847KAT6Ac.4709A>T (p.Asp1570Val)
c.4715A>T (p.Asp1572Val)
c.3390A>T
c.4841A>T (p.Asp1614Val)
c.4820A>T (p.Asp1607Val)
c.4727A>T (p.Asp1576Val)
c.3281A>T (p.Asp1094Val)
COSMIC
8g.41933511T>CCA371064848KAT6Ac.4709A>G (p.Asp1570Gly)
c.4715A>G (p.Asp1572Gly)
c.3390A>G
c.4841A>G (p.Asp1614Gly)
c.4820A>G (p.Asp1607Gly)
c.4727A>G (p.Asp1576Gly)
c.3281A>G (p.Asp1094Gly)
8g.41933511T>GCA371064850KAT6Ac.4709A>C (p.Asp1570Ala)
c.4715A>C (p.Asp1572Ala)
c.3390A>C
c.4841A>C (p.Asp1614Ala)
c.4820A>C (p.Asp1607Ala)
c.4727A>C (p.Asp1576Ala)
c.3281A>C (p.Asp1094Ala)
8g.41933512C>ACA371064853KAT6Ac.4708G>T (p.Asp1570Tyr)
c.4714G>T (p.Asp1572Tyr)
c.3389G>T
c.4840G>T (p.Asp1614Tyr)
c.4819G>T (p.Asp1607Tyr)
c.4726G>T (p.Asp1576Tyr)
c.3280G>T (p.Asp1094Tyr)
8g.41933512C>GCA371064857KAT6Ac.4708G>C (p.Asp1570His)
c.4714G>C (p.Asp1572His)
c.3389G>C
c.4840G>C (p.Asp1614His)
c.4819G>C (p.Asp1607His)
c.4726G>C (p.Asp1576His)
c.3280G>C (p.Asp1094His)
8g.41933512C>TCA371064855KAT6Ac.4708G>A (p.Asp1570Asn)
c.4714G>A (p.Asp1572Asn)
c.3389G>A
c.4840G>A (p.Asp1614Asn)
c.4819G>A (p.Asp1607Asn)
c.4726G>A (p.Asp1576Asn)
c.3280G>A (p.Asp1094Asn)
ClinVar gnomAD v4 COSMIC

Number of alleles fetched