Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154904812_154905024delCA2695238084F8c.5378_5586+4del
c.5273_5481+4del
Xg.154904876_154904889delCA1139532049F8c.5508_5521del (p.Trp1836Ter)
c.5403_5416del (p.Trp1801Ter)
Xg.154904883C>ACA519357160F8c.5514G>T (p.Val1838=)
c.5409G>T (p.Val1803=)
Xg.154904883C=CA2466828437F8c.5514G= (p.Val1838=)
c.5409G= (p.Val1803=)
Xg.154904883C>GCA519357162F8c.5514G>C (p.Val1838=)
c.5409G>C (p.Val1803=)
Xg.154904883C>TCA519357164F8c.5514G>A (p.Val1838=)
c.5409G>A (p.Val1803=)
dbSNP gnomAD v4
Xg.154904884A>CCA414908650F8c.5513T>G (p.Val1838Gly)
c.5408T>G (p.Val1803Gly)
Xg.154904884A>GCA414908652F8c.5513T>C (p.Val1838Ala)
c.5408T>C (p.Val1803Ala)
Xg.154904884A>TCA414908651F8c.5513T>A (p.Val1838Glu)
c.5408T>A (p.Val1803Glu)
Xg.154904885C>ACA414908653F8c.5512G>T (p.Val1838Leu)
c.5407G>T (p.Val1803Leu)
gnomAD v4 COSMIC COSMIC
Xg.154904885C>GCA414908654F8c.5512G>C (p.Val1838Leu)
c.5407G>C (p.Val1803Leu)
Xg.154904885C>TCA414908655F8c.5512G>A (p.Val1838Met)
c.5407G>A (p.Val1803Met)
gnomAD v4
Xg.154904886T>ACA414908656F8c.5511A>T (p.Lys1837Asn)
c.5406A>T (p.Lys1802Asn)
Xg.154904886T>CCA519357179F8c.5511A>G (p.Lys1837=)
c.5406A>G (p.Lys1802=)
Xg.154904886T>GCA414908657F8c.5511A>C (p.Lys1837Asn)
c.5406A>C (p.Lys1802Asn)
Xg.154904887T>ACA414908658F8c.5510A>T (p.Lys1837Ile)
c.5405A>T (p.Lys1802Ile)
Xg.154904887T>CCA414908659F8c.5510A>G (p.Lys1837Arg)
c.5405A>G (p.Lys1802Arg)
Xg.154904887T>GCA414908660F8c.5510A>C (p.Lys1837Thr)
c.5405A>C (p.Lys1802Thr)
Xg.154904888T>ACA414908661F8c.5509A>T (p.Lys1837Ter)
c.5404A>T (p.Lys1802Ter)
Xg.154904888T>CCA414908662F8c.5509A>G (p.Lys1837Glu)
c.5404A>G (p.Lys1802Glu)
Xg.154904888T>GCA414908663F8c.5509A>C (p.Lys1837Gln)
c.5404A>C (p.Lys1802Gln)
Xg.154904889C>ACA414908664F8c.5508G>T (p.Trp1836Cys)
c.5403G>T (p.Trp1801Cys)
Xg.154904889C>GCA414908666F8c.5508G>C (p.Trp1836Cys)
c.5403G>C (p.Trp1801Cys)
Xg.154904889C>TCA414908665F8c.5508G>A (p.Trp1836Ter)
c.5403G>A (p.Trp1801Ter)
Xg.154904890dupCA2695238122F8c.5508dup (p.Lys1837GlufsTer10)
c.5403dup (p.Lys1802GlufsTer10)
Xg.154904890C>ACA414908667F8c.5507G>T (p.Trp1836Leu)
c.5402G>T (p.Trp1801Leu)
Xg.154904890C=CA2466828439F8c.5507G= (p.Trp1836=)
c.5402G= (p.Trp1801=)
Xg.154904890C>GCA414908668F8c.5507G>C (p.Trp1836Ser)
c.5402G>C (p.Trp1801Ser)
Xg.154904890C>TCA414908669F8c.5507G>A (p.Trp1836Ter)
c.5402G>A (p.Trp1801Ter)
dbSNP
Xg.154904890_154904891delinsCACA2466828438F8c.5506_5507delinsTG (p.Trp1836=)
c.5401_5402delinsTG (p.Trp1801=)
Xg.154904891A=CA2466828440F8c.5506T= (p.Trp1836=)
c.5401T= (p.Trp1801=)
Xg.154904891A>CCA414908670F8c.5506T>G (p.Trp1836Gly)
c.5401T>G (p.Trp1801Gly)
Xg.154904891A>GCA414908671F8c.5506T>C (p.Trp1836Arg)
c.5401T>C (p.Trp1801Arg)
ClinVar dbSNP
Xg.154904891A>TCA414908672F8c.5506T>A (p.Trp1836Arg)
c.5401T>A (p.Trp1801Arg)
Xg.154904894delCA873341329F8c.5506del (p.Trp1836GlyfsTer?)
c.5401del (p.Trp1801GlyfsTer?)
dbSNP
Xg.154904892A>CCA414908673F8c.5505T>G (p.Phe1835Leu)
c.5400T>G (p.Phe1800Leu)
Xg.154904892A>GCA519357212F8c.5505T>C (p.Phe1835=)
c.5400T>C (p.Phe1800=)
Xg.154904892A>TCA414908674F8c.5505T>A (p.Phe1835Leu)
c.5400T>A (p.Phe1800Leu)
Xg.154904893A>CCA414908676F8c.5504T>G (p.Phe1835Cys)
c.5399T>G (p.Phe1800Cys)
Xg.154904893A>GCA414908677F8c.5504T>C (p.Phe1835Ser)
c.5399T>C (p.Phe1800Ser)
gnomAD v4
Xg.154904893A>TCA414908675F8c.5504T>A (p.Phe1835Tyr)
c.5399T>A (p.Phe1800Tyr)
Xg.154904894A>CCA414908678F8c.5503T>G (p.Phe1835Val)
c.5398T>G (p.Phe1800Val)
Xg.154904894A>GCA414908679F8c.5503T>C (p.Phe1835Leu)
c.5398T>C (p.Phe1800Leu)
Xg.154904894A>TCA414908680F8c.5503T>A (p.Phe1835Ile)
c.5398T>A (p.Phe1800Ile)
Xg.154904894_154904895delinsAGCA2466828441F8c.5502_5503delinsCT (p.Tyr1834=)
c.5397_5398delinsCT (p.Tyr1799=)
Xg.154904895delCA2466828442F8c.5502del (p.Trp1836GlyfsTer?)
c.5397del (p.Trp1801GlyfsTer?)
dbSNP
Xg.154904895G>ACA519357228F8c.5502C>T (p.Tyr1834=)
c.5397C>T (p.Tyr1799=)
dbSNP
Xg.154904895G>CCA414908681F8c.5502C>G (p.Tyr1834Ter)
c.5397C>G (p.Tyr1799Ter)
Xg.154904895G=CA2466828443F8c.5502C= (p.Tyr1834=)
c.5397C= (p.Tyr1799=)
Xg.154904895G>TCA414908682F8c.5502C>A (p.Tyr1834Ter)
c.5397C>A (p.Tyr1799Ter)
Xg.154904896T>ACA414908683F8c.5501A>T (p.Tyr1834Phe)
c.5396A>T (p.Tyr1799Phe)
Xg.154904896T>CCA414908684F8c.5501A>G (p.Tyr1834Cys)
c.5396A>G (p.Tyr1799Cys)
dbSNP
Xg.154904896T>GCA414908685F8c.5501A>C (p.Tyr1834Ser)
c.5396A>C (p.Tyr1799Ser)
Xg.154904896T=CA2466828444F8c.5501A= (p.Tyr1834=)
c.5396A= (p.Tyr1799=)
Xg.154904896dupCA2573055178F8c.5501dup (p.Tyr1834Ter)
c.5396dup (p.Tyr1799Ter)
ClinVar dbSNP
Xg.154904897A=CA2466828445F8c.5500T= (p.Tyr1834=)
c.5395T= (p.Tyr1799=)
Xg.154904897A>CCA414908686F8c.5500T>G (p.Tyr1834Asp)
c.5395T>G (p.Tyr1799Asp)
dbSNP
Xg.154904897A>GCA414908687F8c.5500T>C (p.Tyr1834His)
c.5395T>C (p.Tyr1799His)
gnomAD v4
Xg.154904897A>TCA414908688F8c.5500T>A (p.Tyr1834Asn)
c.5395T>A (p.Tyr1799Asn)
Xg.154904898A>CCA519357247F8c.5499T>G (p.Thr1833=)
c.5394T>G (p.Thr1798=)
Xg.154904898A>GCA519357244F8c.5499T>C (p.Thr1833=)
c.5394T>C (p.Thr1798=)
Xg.154904898A>TCA519357240F8c.5499T>A (p.Thr1833=)
c.5394T>A (p.Thr1798=)
Xg.154904899G>ACA414908691F8c.5498C>T (p.Thr1833Ile)
c.5393C>T (p.Thr1798Ile)
Xg.154904899G>CCA414908689F8c.5498C>G (p.Thr1833Ser)
c.5393C>G (p.Thr1798Ser)
Xg.154904899G>TCA414908690F8c.5498C>A (p.Thr1833Asn)
c.5393C>A (p.Thr1798Asn)
Xg.154904900T>ACA414908692F8c.5497A>T (p.Thr1833Ser)
c.5392A>T (p.Thr1798Ser)
Xg.154904900T>CCA414908693F8c.5497A>G (p.Thr1833Ala)
c.5392A>G (p.Thr1798Ala)
Xg.154904900T>GCA414908694F8c.5497A>C (p.Thr1833Pro)
c.5392A>C (p.Thr1798Pro)
Xg.154904901T>ACA414908695F8c.5496A>T (p.Lys1832Asn)
c.5391A>T (p.Lys1797Asn)
Xg.154904901T>CCA519357263F8c.5496A>G (p.Lys1832=)
c.5391A>G (p.Lys1797=)
Xg.154904901T>GCA414908696F8c.5496A>C (p.Lys1832Asn)
c.5391A>C (p.Lys1797Asn)
Xg.154904902T>ACA414908697F8c.5495A>T (p.Lys1832Ile)
c.5390A>T (p.Lys1797Ile)
Xg.154904902T>CCA414908698F8c.5495A>G (p.Lys1832Arg)
c.5390A>G (p.Lys1797Arg)
Xg.154904902T>GCA414908699F8c.5495A>C (p.Lys1832Thr)
c.5390A>C (p.Lys1797Thr)
Xg.154904903T>ACA414908700F8c.5494A>T (p.Lys1832Ter)
c.5389A>T (p.Lys1797Ter)
Xg.154904903T>CCA414908701F8c.5494A>G (p.Lys1832Glu)
c.5389A>G (p.Lys1797Glu)
Xg.154904903T>GCA414908702F8c.5494A>C (p.Lys1832Gln)
c.5389A>C (p.Lys1797Gln)
Xg.154904904G>ACA519357273F8c.5493C>T (p.Thr1831=)
c.5388C>T (p.Thr1796=)
dbSNP gnomAD v3 gnomAD v4
Xg.154904904G>CCA519357276F8c.5493C>G (p.Thr1831=)
c.5388C>G (p.Thr1796=)
ClinVar dbSNP
Xg.154904904G=CA2466828446F8c.5493C= (p.Thr1831=)
c.5388C= (p.Thr1796=)
Xg.154904904G>TCA519357277F8c.5493C>A (p.Thr1831=)
c.5388C>A (p.Thr1796=)
gnomAD v4
Xg.154904905G>ACA414908705F8c.5492C>T (p.Thr1831Ile)
c.5387C>T (p.Thr1796Ile)
Xg.154904905G>CCA414908704F8c.5492C>G (p.Thr1831Ser)
c.5387C>G (p.Thr1796Ser)
Xg.154904905G>TCA414908703F8c.5492C>A (p.Thr1831Asn)
c.5387C>A (p.Thr1796Asn)
Xg.154904906T>ACA414908706F8c.5491A>T (p.Thr1831Ser)
c.5386A>T (p.Thr1796Ser)
Xg.154904906T>CCA414908707F8c.5491A>G (p.Thr1831Ala)
c.5386A>G (p.Thr1796Ala)
Xg.154904906T>GCA414908708F8c.5491A>C (p.Thr1831Pro)
c.5386A>C (p.Thr1796Pro)
Xg.154904907T>ACA414908709F8c.5490A>T (p.Glu1830Asp)
c.5385A>T (p.Glu1795Asp)
Xg.154904907T>CCA10567966F8c.5490A>G (p.Glu1830=)
c.5385A>G (p.Glu1795=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154904907T>GCA414908710F8c.5490A>C (p.Glu1830Asp)
c.5385A>C (p.Glu1795Asp)
Xg.154904907T=CA2466828447F8c.5490A= (p.Glu1830=)
c.5385A= (p.Glu1795=)
Xg.154904908T>ACA414908713F8c.5489A>T (p.Glu1830Val)
c.5384A>T (p.Glu1795Val)
Xg.154904908T>CCA414908711F8c.5489A>G (p.Glu1830Gly)
c.5384A>G (p.Glu1795Gly)
Xg.154904908T>GCA414908712F8c.5489A>C (p.Glu1830Ala)
c.5384A>C (p.Glu1795Ala)
Xg.154904909C>ACA414908714F8c.5488G>T (p.Glu1830Ter)
c.5383G>T (p.Glu1795Ter)
ClinVar
Xg.154904909C>GCA414908715F8c.5488G>C (p.Glu1830Gln)
c.5383G>C (p.Glu1795Gln)
gnomAD v4
Xg.154904909C>TCA414908716F8c.5488G>A (p.Glu1830Lys)
c.5383G>A (p.Glu1795Lys)
COSMIC COSMIC
Xg.154904910A=CA2466828448F8c.5487T= (p.Asn1829=)
c.5382T= (p.Asn1794=)
Xg.154904910A>CCA10567967F8c.5487T>G (p.Asn1829Lys)
c.5382T>G (p.Asn1794Lys)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.154904910A>GCA519357302F8c.5487T>C (p.Asn1829=)
c.5382T>C (p.Asn1794=)
gnomAD v4
Xg.154904910A>TCA414908717F8c.5487T>A (p.Asn1829Lys)
c.5382T>A (p.Asn1794Lys)
Xg.154904911T>ACA414908718F8c.5486A>T (p.Asn1829Ile)
c.5381A>T (p.Asn1794Ile)
Xg.154904911T>CCA414908720F8c.5486A>G (p.Asn1829Ser)
c.5381A>G (p.Asn1794Ser)
Xg.154904911T>GCA414908719F8c.5486A>C (p.Asn1829Thr)
c.5381A>C (p.Asn1794Thr)
Xg.154904912delCA2695238128F8c.5486del (p.Asn1829MetfsTer?)
c.5381del (p.Asn1794MetfsTer?)
Xg.154904912T>ACA414908721F8c.5485A>T (p.Asn1829Tyr)
c.5380A>T (p.Asn1794Tyr)
Xg.154904912T>CCA414908722F8c.5485A>G (p.Asn1829Asp)
c.5380A>G (p.Asn1794Asp)
gnomAD v4
Xg.154904912T>GCA414908723F8c.5485A>C (p.Asn1829His)
c.5380A>C (p.Asn1794His)
Xg.154904913A>CCA519357312F8c.5484T>G (p.Pro1828=)
c.5379T>G (p.Pro1793=)
Xg.154904913A>GCA519357314F8c.5484T>C (p.Pro1828=)
c.5379T>C (p.Pro1793=)
Xg.154904913A>TCA519357320F8c.5484T>A (p.Pro1828=)
c.5379T>A (p.Pro1793=)
Xg.154904913_154904914delinsAGCA2466828449F8c.5483_5484delinsCT (p.Pro1828=)
c.5378_5379delinsCT (p.Pro1793=)
Xg.154904914G>ACA414908724F8c.5483C>T (p.Pro1828Leu)
c.5378C>T (p.Pro1793Leu)
Xg.154904914G>CCA414908725F8c.5483C>G (p.Pro1828Arg)
c.5378C>G (p.Pro1793Arg)
Xg.154904914G>TCA414908726F8c.5483C>A (p.Pro1828His)
c.5378C>A (p.Pro1793His)
Xg.154904915delCA1139667916F8c.5483del (p.Pro1828LeufsTer?)
c.5378del (p.Pro1793LeufsTer?)
ClinVar dbSNP
Xg.154904915G>ACA414908727F8c.5482C>T (p.Pro1828Ser)
c.5377C>T (p.Pro1793Ser)
Xg.154904915G>CCA414908728F8c.5482C>G (p.Pro1828Ala)
c.5377C>G (p.Pro1793Ala)
Xg.154904915G>TCA414908729F8c.5482C>A (p.Pro1828Thr)
c.5377C>A (p.Pro1793Thr)
gnomAD v4
Xg.154904916C>ACA414908730F8c.5481G>T (p.Lys1827Asn)
c.5376G>T (p.Lys1792Asn)
Xg.154904916C>GCA414908731F8c.5481G>C (p.Lys1827Asn)
c.5376G>C (p.Lys1792Asn)
Xg.154904916C>TCA519357337F8c.5481G>A (p.Lys1827=)
c.5376G>A (p.Lys1792=)
Xg.154904917T>ACA414908732F8c.5480A>T (p.Lys1827Met)
c.5375A>T (p.Lys1792Met)
Xg.154904917T>CCA414908734F8c.5480A>G (p.Lys1827Arg)
c.5375A>G (p.Lys1792Arg)
Xg.154904917T>GCA414908733F8c.5480A>C (p.Lys1827Thr)
c.5375A>C (p.Lys1792Thr)
Xg.154904918delCA2695238130F8c.5480del (p.Lys1827SerfsTer?)
c.5375del (p.Lys1792SerfsTer?)
Xg.154904918T>ACA255172F8c.5479A>T (p.Lys1827Ter)
c.5374A>T (p.Lys1792Ter)
ClinVar dbSNP
Xg.154904918T>CCA414908735F8c.5479A>G (p.Lys1827Glu)
c.5374A>G (p.Lys1792Glu)
Xg.154904918T>GCA414908736F8c.5479A>C (p.Lys1827Gln)
c.5374A>C (p.Lys1792Gln)
Xg.154904918T=CA2466828450F8c.5479A= (p.Lys1827=)
c.5374A= (p.Lys1792=)
Xg.154904919G>ACA519357355F8c.5478C>T (p.Val1826=)
c.5373C>T (p.Val1791=)
Xg.154904919G>CCA519357353F8c.5478C>G (p.Val1826=)
c.5373C>G (p.Val1791=)
Xg.154904919G>TCA519357350F8c.5478C>A (p.Val1826=)
c.5373C>A (p.Val1791=)
gnomAD v4
Xg.154904920_154904925delCA2695238132F8c.5473_5478del (p.Phe1825_Val1826del)
c.5368_5373del (p.Phe1790_Val1791del)
Xg.154904920A>CCA414908737F8c.5477T>G (p.Val1826Gly)
c.5372T>G (p.Val1791Gly)
Xg.154904920A>GCA414908738F8c.5477T>C (p.Val1826Ala)
c.5372T>C (p.Val1791Ala)
Xg.154904920A>TCA414908739F8c.5477T>A (p.Val1826Asp)
c.5372T>A (p.Val1791Asp)
Xg.154904921C>ACA414908740F8c.5476G>T (p.Val1826Phe)
c.5371G>T (p.Val1791Phe)
dbSNP
Xg.154904921C=CA2466828451F8c.5476G= (p.Val1826=)
c.5371G= (p.Val1791=)
Xg.154904921C>GCA414908741F8c.5476G>C (p.Val1826Leu)
c.5371G>C (p.Val1791Leu)
Xg.154904921C>TCA414908742F8c.5476G>A (p.Val1826Ile)
c.5371G>A (p.Val1791Ile)
Xg.154904922A=CA2466828452F8c.5475T= (p.Phe1825=)
c.5370T= (p.Phe1790=)
Xg.154904922A>CCA414908743F8c.5475T>G (p.Phe1825Leu)
c.5370T>G (p.Phe1790Leu)
Xg.154904922A>GCA519357372F8c.5475T>C (p.Phe1825=)
c.5370T>C (p.Phe1790=)
dbSNP gnomAD v2 gnomAD v4
Xg.154904922A>TCA414908744F8c.5475T>A (p.Phe1825Leu)
c.5370T>A (p.Phe1790Leu)
Xg.154904924dupCA2695238134F8c.5475dup (p.Val1826CysfsTer4)
c.5370dup (p.Val1791CysfsTer4)
Xg.154904923_154904924delCA2695238133F8c.5474_5475del (p.Phe1825CysfsTer4)
c.5369_5370del (p.Phe1790CysfsTer4)
Xg.154904923A>CCA414908747F8c.5474T>G (p.Phe1825Cys)
c.5369T>G (p.Phe1790Cys)
COSMIC COSMIC
Xg.154904923A>GCA414908745F8c.5474T>C (p.Phe1825Ser)
c.5369T>C (p.Phe1790Ser)
Xg.154904923A>TCA414908746F8c.5474T>A (p.Phe1825Tyr)
c.5369T>A (p.Phe1790Tyr)
Xg.154904924A>CCA414908748F8c.5473T>G (p.Phe1825Val)
c.5368T>G (p.Phe1790Val)
gnomAD v4
Xg.154904924A>GCA414908749F8c.5473T>C (p.Phe1825Leu)
c.5368T>C (p.Phe1790Leu)
Xg.154904924A>TCA414908750F8c.5473T>A (p.Phe1825Ile)
c.5368T>A (p.Phe1790Ile)
Xg.154904925G>ACA519357387F8c.5472C>T (p.Asn1824=)
c.5367C>T (p.Asn1789=)
gnomAD v4
Xg.154904925G>CCA414908751F8c.5472C>G (p.Asn1824Lys)
c.5367C>G (p.Asn1789Lys)
Xg.154904925G=CA2466828453F8c.5472C= (p.Asn1824=)
c.5367C= (p.Asn1789=)
Xg.154904925G>TCA414908752F8c.5472C>A (p.Asn1824Lys)
c.5367C>A (p.Asn1789Lys)
Xg.154904926T>ACA414908753F8c.5471A>T (p.Asn1824Ile)
c.5366A>T (p.Asn1789Ile)
COSMIC COSMIC
Xg.154904926T>CCA414908754F8c.5471A>G (p.Asn1824Ser)
c.5366A>G (p.Asn1789Ser)
Xg.154904926T>GCA10567968F8c.5471A>C (p.Asn1824Thr)
c.5366A>C (p.Asn1789Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154904926T=CA2466828454F8c.5471A= (p.Asn1824=)
c.5366A= (p.Asn1789=)
Xg.154904931dupCA645614554F8c.5471dup (p.Asn1824LysfsTer6)
c.5366dup (p.Asn1789LysfsTer6)
dbSNP COSMIC COSMIC COSMIC COSMIC
Xg.154904931delCA2695238135F8c.5471del (p.Asn1824ThrfsTer?)
c.5366del (p.Asn1789ThrfsTer?)
Xg.154904927T>ACA414908755F8c.5470A>T (p.Asn1824Tyr)
c.5365A>T (p.Asn1789Tyr)
Xg.154904927T>CCA414908756F8c.5470A>G (p.Asn1824Asp)
c.5365A>G (p.Asn1789Asp)
Xg.154904927T>GCA414908757F8c.5470A>C (p.Asn1824His)
c.5365A>C (p.Asn1789His)
dbSNP gnomAD v4
Xg.154904927T=CA2466828455F8c.5470A= (p.Asn1824=)
c.5365A= (p.Asn1789=)
Xg.154904928T>ACA414908759F8c.5469A>T (p.Lys1823Asn)
c.5364A>T (p.Lys1788Asn)
Xg.154904928T>CCA519357403F8c.5469A>G (p.Lys1823=)
c.5364A>G (p.Lys1788=)
Xg.154904928T>GCA414908758F8c.5469A>C (p.Lys1823Asn)
c.5364A>C (p.Lys1788Asn)
Xg.154904929T>ACA414908760F8c.5468A>T (p.Lys1823Ile)
c.5363A>T (p.Lys1788Ile)
Xg.154904929T>CCA414908762F8c.5468A>G (p.Lys1823Arg)
c.5363A>G (p.Lys1788Arg)
Xg.154904929T>GCA414908761F8c.5468A>C (p.Lys1823Thr)
c.5363A>C (p.Lys1788Thr)
Xg.154904930T>ACA414908763F8c.5467A>T (p.Lys1823Ter)
c.5362A>T (p.Lys1788Ter)
Xg.154904930T>CCA10567969F8c.5467A>G (p.Lys1823Glu)
c.5362A>G (p.Lys1788Glu)
dbSNP ExAC gnomAD v4
Xg.154904930T>GCA414908764F8c.5467A>C (p.Lys1823Gln)
c.5362A>C (p.Lys1788Gln)
Xg.154904930T=CA2466828456F8c.5467A= (p.Lys1823=)
c.5362A= (p.Lys1788=)
Xg.154904931T>ACA414908765F8c.5466A>T (p.Arg1822Ser)
c.5361A>T (p.Arg1787Ser)
Xg.154904931T>CCA519357417F8c.5466A>G (p.Arg1822=)
c.5361A>G (p.Arg1787=)
dbSNP gnomAD v4
Xg.154904931T>GCA414908766F8c.5466A>C (p.Arg1822Ser)
c.5361A>C (p.Arg1787Ser)
Xg.154904931T=CA2466828457F8c.5466A= (p.Arg1822=)
c.5361A= (p.Arg1787=)
Xg.154904932C>ACA414908767F8c.5465G>T (p.Arg1822Ile)
c.5360G>T (p.Arg1787Ile)
Xg.154904932C>GCA414908768F8c.5465G>C (p.Arg1822Thr)
c.5360G>C (p.Arg1787Thr)
Xg.154904932C>TCA414908769F8c.5465G>A (p.Arg1822Lys)
c.5360G>A (p.Arg1787Lys)
Xg.154904932_154904933insACA519357427F8c.5464_5465insT (p.Arg1822MetfsTer8)
c.5359_5360insT (p.Arg1787MetfsTer8)
Xg.154904933delCA2695238138F8c.5464del (p.Arg1822GlufsTer?)
c.5359del (p.Arg1787GlufsTer?)
Xg.154904933T>ACA414908770F8c.5464A>T (p.Arg1822Ter)
c.5359A>T (p.Arg1787Ter)
Xg.154904933T>CCA414908771F8c.5464A>G (p.Arg1822Gly)
c.5359A>G (p.Arg1787Gly)
Xg.154904933T>GCA519357433F8c.5464A>C (p.Arg1822=)
c.5359A>C (p.Arg1787=)
Xg.154904934A=CA2466828458F8c.5463T= (p.Pro1821=)
c.5358T= (p.Pro1786=)
Xg.154904934A>CCA519357444F8c.5463T>G (p.Pro1821=)
c.5358T>G (p.Pro1786=)
Xg.154904934A>GCA519357441F8c.5463T>C (p.Pro1821=)
c.5358T>C (p.Pro1786=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.154904934A>TCA519357438F8c.5463T>A (p.Pro1821=)
c.5358T>A (p.Pro1786=)
Xg.154904935G>ACA10567970F8c.5462C>T (p.Pro1821Leu)
c.5357C>T (p.Pro1786Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.154904935G>CCA414908772F8c.5462C>G (p.Pro1821Arg)
c.5357C>G (p.Pro1786Arg)
dbSNP gnomAD v2 gnomAD v4
Xg.154904935G=CA2466828459F8c.5462C= (p.Pro1821=)
c.5357C= (p.Pro1786=)
Xg.154904935G>TCA414908773F8c.5462C>A (p.Pro1821His)
c.5357C>A (p.Pro1786His)
Xg.154904936G>ACA414908774F8c.5461C>T (p.Pro1821Ser)
c.5356C>T (p.Pro1786Ser)
Xg.154904936G>CCA414908775F8c.5461C>G (p.Pro1821Ala)
c.5356C>G (p.Pro1786Ala)
Xg.154904936G>TCA414908776F8c.5461C>A (p.Pro1821Thr)
c.5356C>A (p.Pro1786Thr)
gnomAD v4 COSMIC COSMIC
Xg.154904937T>ACA414908777F8c.5460A>T (p.Glu1820Asp)
c.5355A>T (p.Glu1785Asp)
Xg.154904937T>CCA519357454F8c.5460A>G (p.Glu1820=)
c.5355A>G (p.Glu1785=)
Xg.154904937T>GCA414908778F8c.5460A>C (p.Glu1820Asp)
c.5355A>C (p.Glu1785Asp)
Xg.154904938delCA2695238139F8c.5460del (p.Glu1820AspfsTer?)
c.5355del (p.Glu1785AspfsTer?)
Xg.154904938T>ACA414908779F8c.5459A>T (p.Glu1820Val)
c.5354A>T (p.Glu1785Val)
Xg.154904938T>CCA414908781F8c.5459A>G (p.Glu1820Gly)
c.5354A>G (p.Glu1785Gly)
Xg.154904938T>GCA414908780F8c.5459A>C (p.Glu1820Ala)
c.5354A>C (p.Glu1785Ala)
Xg.154904939C>ACA414908782F8c.5458G>T (p.Glu1820Ter)
c.5353G>T (p.Glu1785Ter)
Xg.154904939C>GCA414908783F8c.5458G>C (p.Glu1820Gln)
c.5353G>C (p.Glu1785Gln)
Xg.154904939C>TCA414908784F8c.5458G>A (p.Glu1820Lys)
c.5353G>A (p.Glu1785Lys)
Xg.154904940T>ACA519357459F8c.5457A>T (p.Ala1819=)
c.5352A>T (p.Ala1784=)
Xg.154904940T>CCA519357464F8c.5457A>G (p.Ala1819=)
c.5352A>G (p.Ala1784=)
gnomAD v4
Xg.154904940T>GCA519357461F8c.5457A>C (p.Ala1819=)
c.5352A>C (p.Ala1784=)
Xg.154904941G>ACA414908785F8c.5456C>T (p.Ala1819Val)
c.5351C>T (p.Ala1784Val)
Xg.154904941G>CCA414908786F8c.5456C>G (p.Ala1819Gly)
c.5351C>G (p.Ala1784Gly)
Xg.154904941G>TCA414908787F8c.5456C>A (p.Ala1819Glu)
c.5351C>A (p.Ala1784Glu)
Xg.154904942C>ACA414908788F8c.5455G>T (p.Ala1819Ser)
c.5350G>T (p.Ala1784Ser)
Xg.154904942C>GCA414908789F8c.5455G>C (p.Ala1819Pro)
c.5350G>C (p.Ala1784Pro)
Xg.154904942C>TCA414908790F8c.5455G>A (p.Ala1819Thr)
c.5350G>A (p.Ala1784Thr)
gnomAD v4
Xg.154904943_154904944dupCA2695238141F8c.5454_5455dup (p.Ala1819GlufsTer?)
c.5349_5350dup (p.Ala1784GlufsTer?)
Xg.154904943T>ACA519357477F8c.5454A>T (p.Gly1818=)
c.5349A>T (p.Gly1783=)
Xg.154904943T>CCA519357478F8c.5454A>G (p.Gly1818=)
c.5349A>G (p.Gly1783=)
Xg.154904943T>GCA519357480F8c.5454A>C (p.Gly1818=)
c.5349A>C (p.Gly1783=)
Xg.154904944C>ACA414908791F8c.5453G>T (p.Gly1818Val)
c.5348G>T (p.Gly1783Val)
Xg.154904944C=CA2466828460F8c.5453G= (p.Gly1818=)
c.5348G= (p.Gly1783=)
Xg.154904944C>GCA414908793F8c.5453G>C (p.Gly1818Ala)
c.5348G>C (p.Gly1783Ala)
Xg.154904944C>TCA414908792F8c.5453G>A (p.Gly1818Glu)
c.5348G>A (p.Gly1783Glu)
dbSNP
Xg.154904945dupCA2825002936F8c.5453dup (p.Ala1819SerfsTer4)
c.5348dup (p.Ala1784SerfsTer4)
ClinVar
Xg.154904944_154905247delinsACA2580612537F8c.5374-224_5453delinsT
c.5269-224_5348delinsT
ClinVar
Xg.154904945C>ACA414908794F8c.5452G>T (p.Gly1818Ter)
c.5347G>T (p.Gly1783Ter)
Xg.154904945C>GCA414908795F8c.5452G>C (p.Gly1818Arg)
c.5347G>C (p.Gly1783Arg)
Xg.154904945C>TCA414908796F8c.5452G>A (p.Gly1818Arg)
c.5347G>A (p.Gly1783Arg)
Xg.154904946T>ACA414908797F8c.5451A>T (p.Gln1817His)
c.5346A>T (p.Gln1782His)
Xg.154904946T>CCA519357496F8c.5451A>G (p.Gln1817=)
c.5346A>G (p.Gln1782=)
Xg.154904946T>GCA414908798F8c.5451A>C (p.Gln1817His)
c.5346A>C (p.Gln1782His)
Xg.154904947T>ACA414908799F8c.5450A>T (p.Gln1817Leu)
c.5345A>T (p.Gln1782Leu)
Xg.154904947T>CCA414908800F8c.5450A>G (p.Gln1817Arg)
c.5345A>G (p.Gln1782Arg)
Xg.154904947T>GCA414908801F8c.5450A>C (p.Gln1817Pro)
c.5345A>C (p.Gln1782Pro)
Xg.154904948G>ACA414908802F8c.5449C>T (p.Gln1817Ter)
c.5344C>T (p.Gln1782Ter)
ClinVar dbSNP
Xg.154904948G>CCA414908803F8c.5449C>G (p.Gln1817Glu)
c.5344C>G (p.Gln1782Glu)
Xg.154904948G>TCA414908804F8c.5449C>A (p.Gln1817Lys)
c.5344C>A (p.Gln1782Lys)
Xg.154904949C>ACA414908805F8c.5448G>T (p.Arg1816Ser)
c.5343G>T (p.Arg1781Ser)
dbSNP
Xg.154904949C=CA2466828461F8c.5448G= (p.Arg1816=)
c.5343G= (p.Arg1781=)
Xg.154904949C>GCA414908806F8c.5448G>C (p.Arg1816Ser)
c.5343G>C (p.Arg1781Ser)
Xg.154904949C>TCA519357511F8c.5448G>A (p.Arg1816=)
c.5343G>A (p.Arg1781=)
dbSNP gnomAD v2 gnomAD v4
Xg.154904950C>ACA414908807F8c.5447G>T (p.Arg1816Met)
c.5342G>T (p.Arg1781Met)
Xg.154904950C>GCA414908808F8c.5447G>C (p.Arg1816Thr)
c.5342G>C (p.Arg1781Thr)
Xg.154904950C>TCA414908809F8c.5447G>A (p.Arg1816Lys)
c.5342G>A (p.Arg1781Lys)
Xg.154904951T>ACA414908810F8c.5446A>T (p.Arg1816Trp)
c.5341A>T (p.Arg1781Trp)
Xg.154904951T>CCA414908811F8c.5446A>G (p.Arg1816Gly)
c.5341A>G (p.Arg1781Gly)
Xg.154904951T>GCA519357524F8c.5446A>C (p.Arg1816=)
c.5341A>C (p.Arg1781=)
Xg.154904952C>ACA414908812F8c.5445G>T (p.Gln1815His)
c.5340G>T (p.Gln1780His)
Xg.154904952C>GCA414908813F8c.5445G>C (p.Gln1815His)
c.5340G>C (p.Gln1780His)
Xg.154904952C>TCA519357529F8c.5445G>A (p.Gln1815=)
c.5340G>A (p.Gln1780=)
Xg.154904953T>ACA414908814F8c.5444A>T (p.Gln1815Leu)
c.5339A>T (p.Gln1780Leu)
Xg.154904953T>CCA414908815F8c.5444A>G (p.Gln1815Arg)
c.5339A>G (p.Gln1780Arg)
dbSNP
Xg.154904953T>GCA414908816F8c.5444A>C (p.Gln1815Pro)
c.5339A>C (p.Gln1780Pro)
Xg.154904953T=CA2466828462F8c.5444A= (p.Gln1815=)
c.5339A= (p.Gln1780=)
Xg.154904954G>ACA255167F8c.5443C>T (p.Gln1815Ter)
c.5338C>T (p.Gln1780Ter)
ClinVar dbSNP
Xg.154904954G>CCA414908818F8c.5443C>G (p.Gln1815Glu)
c.5338C>G (p.Gln1780Glu)
Xg.154904954G=CA2466828463F8c.5443C= (p.Gln1815=)
c.5338C= (p.Gln1780=)
Xg.154904954G>TCA414908817F8c.5443C>A (p.Gln1815Lys)
c.5338C>A (p.Gln1780Lys)
Xg.154904955A>CCA414908820F8c.5442T>G (p.Asp1814Glu)
c.5337T>G (p.Asp1779Glu)
Xg.154904955A>GCA519357543F8c.5442T>C (p.Asp1814=)
c.5337T>C (p.Asp1779=)
Xg.154904955A>TCA414908819F8c.5442T>A (p.Asp1814Glu)
c.5337T>A (p.Asp1779Glu)
Xg.154904956T>ACA414908821F8c.5441A>T (p.Asp1814Val)
c.5336A>T (p.Asp1779Val)
ClinVar dbSNP
Xg.154904956T>CCA414908822F8c.5441A>G (p.Asp1814Gly)
c.5336A>G (p.Asp1779Gly)
COSMIC COSMIC
Xg.154904956T>GCA414908823F8c.5441A>C (p.Asp1814Ala)
c.5336A>C (p.Asp1779Ala)
Xg.154904956T=CA2466828464F8c.5441A= (p.Asp1814=)
c.5336A= (p.Asp1779=)
Xg.154904957C>ACA414908824F8c.5440G>T (p.Asp1814Tyr)
c.5335G>T (p.Asp1779Tyr)
Xg.154904957C>GCA414908825F8c.5440G>C (p.Asp1814His)
c.5335G>C (p.Asp1779His)
Xg.154904957C>TCA414908826F8c.5440G>A (p.Asp1814Asn)
c.5335G>A (p.Asp1779Asn)
Xg.154904958T>ACA414908827F8c.5439A>T (p.Glu1813Asp)
c.5334A>T (p.Glu1778Asp)
Xg.154904958T>CCA519357559F8c.5439A>G (p.Glu1813=)
c.5334A>G (p.Glu1778=)
Xg.154904958T>GCA414908828F8c.5439A>C (p.Glu1813Asp)
c.5334A>C (p.Glu1778Asp)
Xg.154904959T>ACA414908830F8c.5438A>T (p.Glu1813Val)
c.5333A>T (p.Glu1778Val)
Xg.154904959T>CCA414908831F8c.5438A>G (p.Glu1813Gly)
c.5333A>G (p.Glu1778Gly)
Xg.154904959T>GCA414908832F8c.5438A>C (p.Glu1813Ala)
c.5333A>C (p.Glu1778Ala)
Xg.154904960C>ACA414908835F8c.5437G>T (p.Glu1813Ter)
c.5332G>T (p.Glu1778Ter)
Xg.154904960C>GCA414908833F8c.5437G>C (p.Glu1813Gln)
c.5332G>C (p.Glu1778Gln)
Xg.154904960C>TCA414908834F8c.5437G>A (p.Glu1813Lys)
c.5332G>A (p.Glu1778Lys)
gnomAD v4
Xg.154904961C>ACA414908836F8c.5436G>T (p.Glu1812Asp)
c.5331G>T (p.Glu1777Asp)
Xg.154904961C>GCA414908837F8c.5436G>C (p.Glu1812Asp)
c.5331G>C (p.Glu1777Asp)
Xg.154904961C>TCA519357572F8c.5436G>A (p.Glu1812=)
c.5331G>A (p.Glu1777=)
COSMIC COSMIC
Xg.154904962T>ACA414908838F8c.5435A>T (p.Glu1812Val)
c.5330A>T (p.Glu1777Val)
Xg.154904962T>CCA414908839F8c.5435A>G (p.Glu1812Gly)
c.5330A>G (p.Glu1777Gly)
Xg.154904962T>GCA414908840F8c.5435A>C (p.Glu1812Ala)
c.5330A>C (p.Glu1777Ala)
Xg.154904963C>ACA414908841F8c.5434G>T (p.Glu1812Ter)
c.5329G>T (p.Glu1777Ter)
dbSNP
Xg.154904963C=CA2466828465F8c.5434G= (p.Glu1812=)
c.5329G= (p.Glu1777=)
Xg.154904963C>GCA414908842F8c.5434G>C (p.Glu1812Gln)
c.5329G>C (p.Glu1777Gln)
Xg.154904963C>TCA10567971F8c.5434G>A (p.Glu1812Lys)
c.5329G>A (p.Glu1777Lys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154904964A=CA2466828466F8c.5433T= (p.Tyr1811=)
c.5328T= (p.Tyr1776=)
Xg.154904964A>CCA414908843F8c.5433T>G (p.Tyr1811Ter)
c.5328T>G (p.Tyr1776Ter)
Xg.154904964A>GCA519357588F8c.5433T>C (p.Tyr1811=)
c.5328T>C (p.Tyr1776=)
dbSNP gnomAD v2 gnomAD v4
Xg.154904964A>TCA414908844F8c.5433T>A (p.Tyr1811Ter)
c.5328T>A (p.Tyr1776Ter)
Xg.154904965T>ACA414908848F8c.5432A>T (p.Tyr1811Phe)
c.5327A>T (p.Tyr1776Phe)
Xg.154904965T>CCA414908846F8c.5432A>G (p.Tyr1811Cys)
c.5327A>G (p.Tyr1776Cys)
Xg.154904965T>GCA414908845F8c.5432A>C (p.Tyr1811Ser)
c.5327A>C (p.Tyr1776Ser)
gnomAD v4
Xg.154904966A>CCA414908857F8c.5431T>G (p.Tyr1811Asp)
c.5326T>G (p.Tyr1776Asp)
Xg.154904966A>GCA414908859F8c.5431T>C (p.Tyr1811His)
c.5326T>C (p.Tyr1776His)
Xg.154904966A>TCA414908861F8c.5431T>A (p.Tyr1811Asn)
c.5326T>A (p.Tyr1776Asn)
Xg.154904967A=CA2466828467F8c.5430T= (p.Ser1810=)
c.5325T= (p.Ser1775=)
Xg.154904967A>CCA10567972F8c.5430T>G (p.Ser1810=)
c.5325T>G (p.Ser1775=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154904967A>GCA519357602F8c.5430T>C (p.Ser1810=)
c.5325T>C (p.Ser1775=)
Xg.154904967A>TCA519357605F8c.5430T>A (p.Ser1810=)
c.5325T>A (p.Ser1775=)
gnomAD v4
Xg.154904968G>ACA414908868F8c.5429C>T (p.Ser1810Phe)
c.5324C>T (p.Ser1775Phe)
Xg.154904968G>CCA414908870F8c.5429C>G (p.Ser1810Cys)
c.5324C>G (p.Ser1775Cys)
Xg.154904968G>TCA414908871F8c.5429C>A (p.Ser1810Tyr)
c.5324C>A (p.Ser1775Tyr)
Xg.154904969A>CCA414908874F8c.5428T>G (p.Ser1810Ala)
c.5323T>G (p.Ser1775Ala)
Xg.154904969A>GCA414908876F8c.5428T>C (p.Ser1810Pro)
c.5323T>C (p.Ser1775Pro)
COSMIC COSMIC
Xg.154904969A>TCA414908879F8c.5428T>A (p.Ser1810Thr)
c.5323T>A (p.Ser1775Thr)
Xg.154904971delCA2695238148F8c.5428del (p.Ser1810LeufsTer?)
c.5323del (p.Ser1775LeufsTer?)
Xg.154904970A=CA2466828468F8c.5427T= (p.Ile1809=)
c.5322T= (p.Ile1774=)
Xg.154904970A>CCA414908880F8c.5427T>G (p.Ile1809Met)
c.5322T>G (p.Ile1774Met)
Xg.154904970A>GCA10567973F8c.5427T>C (p.Ile1809=)
c.5322T>C (p.Ile1774=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154904970A>TCA519357619F8c.5427T>A (p.Ile1809=)
c.5322T>A (p.Ile1774=)
COSMIC COSMIC
Xg.154904971A>CCA414908883F8c.5426T>G (p.Ile1809Ser)
c.5321T>G (p.Ile1774Ser)
Xg.154904971A>GCA414908881F8c.5426T>C (p.Ile1809Thr)
c.5321T>C (p.Ile1774Thr)
Xg.154904971A>TCA414908882F8c.5426T>A (p.Ile1809Asn)
c.5321T>A (p.Ile1774Asn)
Xg.154904972T>ACA414908885F8c.5425A>T (p.Ile1809Phe)
c.5320A>T (p.Ile1774Phe)
Xg.154904972T>CCA414908886F8c.5425A>G (p.Ile1809Val)
c.5320A>G (p.Ile1774Val)
gnomAD v4
Xg.154904972T>GCA414908888F8c.5425A>C (p.Ile1809Leu)
c.5320A>C (p.Ile1774Leu)
Xg.154904973A>CCA519357631F8c.5424T>G (p.Leu1808=)
c.5319T>G (p.Leu1773=)
Xg.154904973A>GCA519357633F8c.5424T>C (p.Leu1808=)
c.5319T>C (p.Leu1773=)
Xg.154904973A>TCA519357636F8c.5424T>A (p.Leu1808=)
c.5319T>A (p.Leu1773=)
Xg.154904974A=CA2466828469F8c.5423T= (p.Leu1808=)
c.5318T= (p.Leu1773=)
Xg.154904974A>CCA414908890F8c.5423T>G (p.Leu1808Arg)
c.5318T>G (p.Leu1773Arg)
Xg.154904974A>GCA10567974F8c.5423T>C (p.Leu1808Pro)
c.5318T>C (p.Leu1773Pro)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.154904974A>TCA414908891F8c.5423T>A (p.Leu1808His)
c.5318T>A (p.Leu1773His)
Xg.154904975G>ACA255166F8c.5422C>T (p.Leu1808Phe)
c.5317C>T (p.Leu1773Phe)
ClinVar dbSNP
Xg.154904975G>CCA414908893F8c.5422C>G (p.Leu1808Val)
c.5317C>G (p.Leu1773Val)
gnomAD v4
Xg.154904975G=CA2466828470F8c.5422C= (p.Leu1808=)
c.5317C= (p.Leu1773=)
Xg.154904975G>TCA414908895F8c.5422C>A (p.Leu1808Ile)
c.5317C>A (p.Leu1773Ile)
COSMIC COSMIC
Xg.154904976delCA2695238153F8c.5422del (p.Ile1809PhefsTer?)
c.5317del (p.Ile1774PhefsTer?)
Xg.154904976G>ACA519357650F8c.5421C>T (p.Ser1807=)
c.5316C>T (p.Ser1772=)
dbSNP
Xg.154904976G>CCA414908899F8c.5421C>G (p.Ser1807Arg)
c.5316C>G (p.Ser1772Arg)
dbSNP
Xg.154904976G=CA2466828471F8c.5421C= (p.Ser1807=)
c.5316C= (p.Ser1772=)
Xg.154904976G>TCA414908900F8c.5421C>A (p.Ser1807Arg)
c.5316C>A (p.Ser1772Arg)
Xg.154904977C>ACA414908903F8c.5420G>T (p.Ser1807Ile)
c.5315G>T (p.Ser1772Ile)
Xg.154904977C>GCA414908904F8c.5420G>C (p.Ser1807Thr)
c.5315G>C (p.Ser1772Thr)
Xg.154904977C>TCA414908902F8c.5420G>A (p.Ser1807Asn)
c.5315G>A (p.Ser1772Asn)
Xg.154904978T>ACA414908905F8c.5419A>T (p.Ser1807Cys)
c.5314A>T (p.Ser1772Cys)
Xg.154904978T>CCA414908907F8c.5419A>G (p.Ser1807Gly)
c.5314A>G (p.Ser1772Gly)
Xg.154904978T>GCA414908908F8c.5419A>C (p.Ser1807Arg)
c.5314A>C (p.Ser1772Arg)
Xg.154904979A>CCA519357662F8c.5418T>G (p.Ser1806=)
c.5313T>G (p.Ser1771=)
Xg.154904979A>GCA519357664F8c.5418T>C (p.Ser1806=)
c.5313T>C (p.Ser1771=)
Xg.154904979A>TCA519357666F8c.5418T>A (p.Ser1806=)
c.5313T>A (p.Ser1771=)
Xg.154904980G>ACA414908914F8c.5417C>T (p.Ser1806Phe)
c.5312C>T (p.Ser1771Phe)
ClinVar dbSNP
Xg.154904980G>CCA414908915F8c.5417C>G (p.Ser1806Cys)
c.5312C>G (p.Ser1771Cys)
Xg.154904980G=CA2466828472F8c.5417C= (p.Ser1806=)
c.5312C= (p.Ser1771=)
Xg.154904980G>TCA414908918F8c.5417C>A (p.Ser1806Tyr)
c.5312C>A (p.Ser1771Tyr)
Xg.154904981A>CCA414908926F8c.5416T>G (p.Ser1806Ala)
c.5311T>G (p.Ser1771Ala)
Xg.154904981A>GCA414908920F8c.5416T>C (p.Ser1806Pro)
c.5311T>C (p.Ser1771Pro)
Xg.154904981A>TCA414908923F8c.5416T>A (p.Ser1806Thr)
c.5311T>A (p.Ser1771Thr)
Xg.154904982A>CCA414908929F8c.5415T>G (p.Tyr1805Ter)
c.5310T>G (p.Tyr1770Ter)
Xg.154904982A>GCA519357671F8c.5415T>C (p.Tyr1805=)
c.5310T>C (p.Tyr1770=)
Xg.154904982A>TCA414908930F8c.5415T>A (p.Tyr1805Ter)
c.5310T>A (p.Tyr1770Ter)
Xg.154904983T>ACA414908934F8c.5414A>T (p.Tyr1805Phe)
c.5309A>T (p.Tyr1770Phe)
dbSNP
Xg.154904983T>CCA414908936F8c.5414A>G (p.Tyr1805Cys)
c.5309A>G (p.Tyr1770Cys)
Xg.154904983T>GCA414908939F8c.5414A>C (p.Tyr1805Ser)
c.5309A>C (p.Tyr1770Ser)
Xg.154904983T=CA2466828473F8c.5414A= (p.Tyr1805=)
c.5309A= (p.Tyr1770=)

Number of alleles fetched