Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.7582933_7587670delinsAGAACAGTCTTCA2580075482 ClinVar
6g.7582933_7587670delinsAGAGAAGAACAGTCTTCA915944145 ClinVar
6g.7582934_7587655delCA2695202641
6g.7583044_7583047delCA2580075503DSPc.4453_4456del (p.Leu1485LysfsTer?)
c.5782_5785del (p.Leu1928LysfsTer?)
c.3985_3988del (p.Leu1329LysfsTer?)
ClinVar
6g.7583043G>ACA448715538DSPc.4452G>A (p.Gln1484=)
c.5781G>A (p.Gln1927=)
c.3984G>A (p.Gln1328=)
6g.7583043G>CCA362689401DSPc.4452G>C (p.Gln1484His)
c.5781G>C (p.Gln1927His)
c.3984G>C (p.Gln1328His)
6g.7583043G>TCA362689402DSPc.4452G>T (p.Gln1484His)
c.5781G>T (p.Gln1927His)
c.3984G>T (p.Gln1328His)
6g.7583044T>ACA362689404DSPc.4453T>A (p.Leu1485Ile)
c.5782T>A (p.Leu1928Ile)
c.3985T>A (p.Leu1329Ile)
6g.7583044T>CCA448715539DSPc.4453T>C (p.Leu1485=)
c.5782T>C (p.Leu1928=)
c.3985T>C (p.Leu1329=)
6g.7583044T>GCA362689403DSPc.4453T>G (p.Leu1485Val)
c.5782T>G (p.Leu1928Val)
c.3985T>G (p.Leu1329Val)
gnomAD v4
6g.7583045T>ACA362689405DSPc.4454T>A (p.Leu1485Ter)
c.5783T>A (p.Leu1928Ter)
c.3986T>A (p.Leu1329Ter)
6g.7583045T>CCA362689406DSPc.4454T>C (p.Leu1485Ser)
c.5783T>C (p.Leu1928Ser)
c.3986T>C (p.Leu1329Ser)
6g.7583045T>GCA362689407DSPc.4454T>G (p.Leu1485Ter)
c.5783T>G (p.Leu1928Ter)
c.3986T>G (p.Leu1329Ter)
6g.7583045_7583051delinsTAGAAACCA1608607004DSPc.4454_4460delinsTAGAAAC (p.Leu1485=)
c.5783_5789delinsTAGAAAC (p.Leu1928=)
c.3986_3992delinsTAGAAAC (p.Leu1329=)
6g.7583046A>CCA362689408DSPc.4455A>C (p.Leu1485Phe)
c.5784A>C (p.Leu1928Phe)
c.3987A>C (p.Leu1329Phe)
6g.7583046A>GCA448715540DSPc.4455A>G (p.Leu1485=)
c.5784A>G (p.Leu1928=)
c.3987A>G (p.Leu1329=)
6g.7583046A>TCA362689409DSPc.4455A>T (p.Leu1485Phe)
c.5784A>T (p.Leu1928Phe)
c.3987A>T (p.Leu1329Phe)
6g.7583050_7583055delCA565358152DSPc.4459_4464del (p.Thr1487_Glu1488del)
c.5788_5793del (p.Thr1930_Glu1931del)
c.3991_3996del (p.Thr1331_Glu1332del)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7583047G>ACA133972315DSPc.4456G>A (p.Glu1486Lys)
c.5785G>A (p.Glu1929Lys)
c.3988G>A (p.Glu1330Lys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7583047G>CCA362689410DSPc.4456G>C (p.Glu1486Gln)
c.5785G>C (p.Glu1929Gln)
c.3988G>C (p.Glu1330Gln)
6g.7583047G=CA1608607012DSPc.4456G= (p.Glu1486=)
c.5785G= (p.Glu1929=)
c.3988G= (p.Glu1330=)
6g.7583047G>TCA362689411DSPc.4456G>T (p.Glu1486Ter)
c.5785G>T (p.Glu1929Ter)
c.3988G>T (p.Glu1330Ter)
6g.7583048A>CCA362689412DSPc.4457A>C (p.Glu1486Ala)
c.5786A>C (p.Glu1929Ala)
c.3989A>C (p.Glu1330Ala)
6g.7583048A>GCA362689413DSPc.4457A>G (p.Glu1486Gly)
c.5786A>G (p.Glu1929Gly)
c.3989A>G (p.Glu1330Gly)
6g.7583048A>TCA362689414DSPc.4457A>T (p.Glu1486Val)
c.5786A>T (p.Glu1929Val)
c.3989A>T (p.Glu1330Val)
6g.7583049A>CCA362689415DSPc.4458A>C (p.Glu1486Asp)
c.5787A>C (p.Glu1929Asp)
c.3990A>C (p.Glu1330Asp)
gnomAD v4
6g.7583049A>GCA448715541DSPc.4458A>G (p.Glu1486=)
c.5787A>G (p.Glu1929=)
c.3990A>G (p.Glu1330=)
6g.7583049A>TCA362689416DSPc.4458A>T (p.Glu1486Asp)
c.5787A>T (p.Glu1929Asp)
c.3990A>T (p.Glu1330Asp)
6g.7583050A>CCA362689419DSPc.4459A>C (p.Thr1487Pro)
c.5788A>C (p.Thr1930Pro)
c.3991A>C (p.Thr1331Pro)
6g.7583050A>GCA362689418DSPc.4459A>G (p.Thr1487Ala)
c.5788A>G (p.Thr1930Ala)
c.3991A>G (p.Thr1331Ala)
COSMIC
6g.7583050A>TCA362689417DSPc.4459A>T (p.Thr1487Ser)
c.5788A>T (p.Thr1930Ser)
c.3991A>T (p.Thr1331Ser)
6g.7583051C>ACA362689420DSPc.4460C>A (p.Thr1487Lys)
c.5789C>A (p.Thr1930Lys)
c.3992C>A (p.Thr1331Lys)
6g.7583051C=CA1608607020DSPc.4460C= (p.Thr1487=)
c.5789C= (p.Thr1930=)
c.3992C= (p.Thr1331=)
6g.7583051C>GCA006614DSPc.4460C>G (p.Thr1487Arg)
c.5789C>G (p.Thr1930Arg)
c.3992C>G (p.Thr1331Arg)
ClinVar dbSNP gnomAD v4
6g.7583051C>TCA362689421DSPc.4460C>T (p.Thr1487Ile)
c.5789C>T (p.Thr1930Ile)
c.3992C>T (p.Thr1331Ile)
6g.7583052A=CA1608607026DSPc.4461A= (p.Thr1487=)
c.5790A= (p.Thr1930=)
c.3993A= (p.Thr1331=)
6g.7583052A>CCA448715580DSPc.4461A>C (p.Thr1487=)
c.5790A>C (p.Thr1930=)
c.3993A>C (p.Thr1331=)
6g.7583052A>GCA448715581DSPc.4461A>G (p.Thr1487=)
c.5790A>G (p.Thr1930=)
c.3993A>G (p.Thr1331=)
ClinVar dbSNP gnomAD v4
6g.7583052A>TCA448715582DSPc.4461A>T (p.Thr1487=)
c.5790A>T (p.Thr1930=)
c.3993A>T (p.Thr1331=)
6g.7583053G>ACA362689422DSPc.4462G>A (p.Glu1488Lys)
c.5791G>A (p.Glu1931Lys)
c.3994G>A (p.Glu1332Lys)
6g.7583053G>CCA362689423DSPc.4462G>C (p.Glu1488Gln)
c.5791G>C (p.Glu1931Gln)
c.3994G>C (p.Glu1332Gln)
6g.7583053G>TCA362689424DSPc.4462G>T (p.Glu1488Ter)
c.5791G>T (p.Glu1931Ter)
c.3994G>T (p.Glu1332Ter)
6g.7583054A>CCA362689425DSPc.4463A>C (p.Glu1488Ala)
c.5792A>C (p.Glu1931Ala)
c.3995A>C (p.Glu1332Ala)
6g.7583054A>GCA362689426DSPc.4463A>G (p.Glu1488Gly)
c.5792A>G (p.Glu1931Gly)
c.3995A>G (p.Glu1332Gly)
6g.7583054A>TCA362689427DSPc.4463A>T (p.Glu1488Val)
c.5792A>T (p.Glu1931Val)
c.3995A>T (p.Glu1332Val)
6g.7583054_7583055insGAGTTAGATACA2677235036DSPc.4463_4464insGAGTTAGATA (p.Arg1489SerfsTer2)
c.5792_5793insGAGTTAGATA (p.Arg1932SerfsTer2)
c.3995_3996insGAGTTAGATA (p.Arg1333SerfsTer2)
gnomAD v4
6g.7583055A>CCA362689428DSPc.4464A>C (p.Glu1488Asp)
c.5793A>C (p.Glu1931Asp)
c.3996A>C (p.Glu1332Asp)
6g.7583055A>GCA448715585DSPc.4464A>G (p.Glu1488=)
c.5793A>G (p.Glu1931=)
c.3996A>G (p.Glu1332=)
6g.7583055A>TCA362689429DSPc.4464A>T (p.Glu1488Asp)
c.5793A>T (p.Glu1931Asp)
c.3996A>T (p.Glu1332Asp)
6g.7583056C>ACA362689430DSPc.4465C>A (p.Arg1489Ser)
c.5794C>A (p.Arg1932Ser)
c.3997C>A (p.Arg1333Ser)
6g.7583056C=CA1608607040DSPc.4465C= (p.Arg1489=)
c.5794C= (p.Arg1932=)
c.3997C= (p.Arg1333=)
6g.7583056C>GCA362689431DSPc.4465C>G (p.Arg1489Gly)
c.5794C>G (p.Arg1932Gly)
c.3997C>G (p.Arg1333Gly)
6g.7583056C>TCA045687DSPc.4465C>T (p.Arg1489Cys)
c.5794C>T (p.Arg1932Cys)
c.3997C>T (p.Arg1333Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
6g.7583057G>ACA045698DSPc.4466G>A (p.Arg1489His)
c.5795G>A (p.Arg1932His)
c.3998G>A (p.Arg1333His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
6g.7583057G>CCA362689433DSPc.4466G>C (p.Arg1489Pro)
c.5795G>C (p.Arg1932Pro)
c.3998G>C (p.Arg1333Pro)
6g.7583057G=CA1608607046DSPc.4466G= (p.Arg1489=)
c.5795G= (p.Arg1932=)
c.3998G= (p.Arg1333=)
6g.7583057G>TCA362689432DSPc.4466G>T (p.Arg1489Leu)
c.5795G>T (p.Arg1932Leu)
c.3998G>T (p.Arg1333Leu)
6g.7583058C>ACA448715587DSPc.4467C>A (p.Arg1489=)
c.5796C>A (p.Arg1932=)
c.3999C>A (p.Arg1333=)
6g.7583058C=CA1608607054DSPc.4467C= (p.Arg1489=)
c.5796C= (p.Arg1932=)
c.3999C= (p.Arg1333=)
6g.7583058C>GCA045714DSPc.4467C>G (p.Arg1489=)
c.5796C>G (p.Arg1932=)
c.3999C>G (p.Arg1333=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7583058C>TCA045726DSPc.4467C>T (p.Arg1489=)
c.5796C>T (p.Arg1932=)
c.3999C>T (p.Arg1333=)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.7583059T>ACA362689434DSPc.4468T>A (p.Ser1490Thr)
c.5797T>A (p.Ser1933Thr)
c.4000T>A (p.Ser1334Thr)
6g.7583059T>CCA362689435DSPc.4468T>C (p.Ser1490Pro)
c.5797T>C (p.Ser1933Pro)
c.4000T>C (p.Ser1334Pro)
6g.7583059T>GCA362689436DSPc.4468T>G (p.Ser1490Ala)
c.5797T>G (p.Ser1933Ala)
c.4000T>G (p.Ser1334Ala)
6g.7583060C>ACA362689437DSPc.4469C>A (p.Ser1490Tyr)
c.5798C>A (p.Ser1933Tyr)
c.4001C>A (p.Ser1334Tyr)
6g.7583060C=CA1608607062DSPc.4469C= (p.Ser1490=)
c.5798C= (p.Ser1933=)
c.4001C= (p.Ser1334=)
6g.7583060C>GCA362689438DSPc.4469C>G (p.Ser1490Cys)
c.5798C>G (p.Ser1933Cys)
c.4001C>G (p.Ser1334Cys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7583060C>TCA133972347DSPc.4469C>T (p.Ser1490Phe)
c.5798C>T (p.Ser1933Phe)
c.4001C>T (p.Ser1334Phe)
ClinVar dbSNP
6g.7583061C>ACA448715589DSPc.4470C>A (p.Ser1490=)
c.5799C>A (p.Ser1933=)
c.4002C>A (p.Ser1334=)
6g.7583061C>GCA448715590DSPc.4470C>G (p.Ser1490=)
c.5799C>G (p.Ser1933=)
c.4002C>G (p.Ser1334=)
6g.7583061C>TCA448715591DSPc.4470C>T (p.Ser1490=)
c.5799C>T (p.Ser1933=)
c.4002C>T (p.Ser1334=)
6g.7583062C>ACA045761DSPc.4471C>A (p.Arg1491=)
c.5800C>A (p.Arg1934=)
c.4003C>A (p.Arg1335=)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.7583062C=CA1608607078DSPc.4471C= (p.Arg1491=)
c.5800C= (p.Arg1934=)
c.4003C= (p.Arg1335=)
6g.7583062C>GCA362689439DSPc.4471C>G (p.Arg1491Gly)
c.5800C>G (p.Arg1934Gly)
c.4003C>G (p.Arg1335Gly)
gnomAD v4
6g.7583062C>TCA006621DSPc.4471C>T (p.Arg1491Ter)
c.5800C>T (p.Arg1934Ter)
c.4003C>T (p.Arg1335Ter)
ClinVar dbSNP
6g.7583063G>ACA362689440DSPc.4472G>A (p.Arg1491Gln)
c.5801G>A (p.Arg1934Gln)
c.4004G>A (p.Arg1335Gln)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
6g.7583063G>CCA362689441DSPc.4472G>C (p.Arg1491Pro)
c.5801G>C (p.Arg1934Pro)
c.4004G>C (p.Arg1335Pro)
6g.7583063G=CA1608607087DSPc.4472G= (p.Arg1491=)
c.5801G= (p.Arg1934=)
c.4004G= (p.Arg1335=)
6g.7583063G>TCA362689442DSPc.4472G>T (p.Arg1491Leu)
c.5801G>T (p.Arg1934Leu)
c.4004G>T (p.Arg1335Leu)
ClinVar
6g.7583064A=CA1608607094DSPc.4473A= (p.Arg1491=)
c.5802A= (p.Arg1934=)
c.4005A= (p.Arg1335=)
6g.7583064A>CCA448715595DSPc.4473A>C (p.Arg1491=)
c.5802A>C (p.Arg1934=)
c.4005A>C (p.Arg1335=)
6g.7583064A>GCA448715596DSPc.4473A>G (p.Arg1491=)
c.5802A>G (p.Arg1934=)
c.4005A>G (p.Arg1335=)
ClinVar dbSNP
6g.7583064A>TCA448715597DSPc.4473A>T (p.Arg1491=)
c.5802A>T (p.Arg1934=)
c.4005A>T (p.Arg1335=)
ClinVar gnomAD v4
6g.7583065T>ACA362689445DSPc.4474T>A (p.Tyr1492Asn)
c.5803T>A (p.Tyr1935Asn)
c.4006T>A (p.Tyr1336Asn)
6g.7583065T>CCA362689443DSPc.4474T>C (p.Tyr1492His)
c.5803T>C (p.Tyr1935His)
c.4006T>C (p.Tyr1336His)
6g.7583065T>GCA362689444DSPc.4474T>G (p.Tyr1492Asp)
c.5803T>G (p.Tyr1935Asp)
c.4006T>G (p.Tyr1336Asp)
6g.7583066A=CA1608607101DSPc.4475A= (p.Tyr1492=)
c.5804A= (p.Tyr1935=)
c.4007A= (p.Tyr1336=)
6g.7583066A>CCA362689446DSPc.4475A>C (p.Tyr1492Ser)
c.5804A>C (p.Tyr1935Ser)
c.4007A>C (p.Tyr1336Ser)
6g.7583066A>GCA045770DSPc.4475A>G (p.Tyr1492Cys)
c.5804A>G (p.Tyr1935Cys)
c.4007A>G (p.Tyr1336Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7583066A>TCA362689447DSPc.4475A>T (p.Tyr1492Phe)
c.5804A>T (p.Tyr1935Phe)
c.4007A>T (p.Tyr1336Phe)
6g.7583067T>ACA362689448DSPc.4476T>A (p.Tyr1492Ter)
c.5805T>A (p.Tyr1935Ter)
c.4008T>A (p.Tyr1336Ter)
6g.7583067T>CCA045784DSPc.4476T>C (p.Tyr1492=)
c.5805T>C (p.Tyr1935=)
c.4008T>C (p.Tyr1336=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7583067T>GCA362689449DSPc.4476T>G (p.Tyr1492Ter)
c.5805T>G (p.Tyr1935Ter)
c.4008T>G (p.Tyr1336Ter)
6g.7583067T=CA1608607105DSPc.4476T= (p.Tyr1492=)
c.5805T= (p.Tyr1935=)
c.4008T= (p.Tyr1336=)
6g.7583068C>ACA362689450DSPc.4477C>A (p.Gln1493Lys)
c.5806C>A (p.Gln1936Lys)
c.4009C>A (p.Gln1337Lys)
6g.7583068C>GCA362689451DSPc.4477C>G (p.Gln1493Glu)
c.5806C>G (p.Gln1936Glu)
c.4009C>G (p.Gln1337Glu)
6g.7583068C>TCA362689452DSPc.4477C>T (p.Gln1493Ter)
c.5806C>T (p.Gln1936Ter)
c.4009C>T (p.Gln1337Ter)
ClinVar dbSNP
6g.7583069A=CA1608607111DSPc.4478A= (p.Gln1493=)
c.5807A= (p.Gln1936=)
c.4010A= (p.Gln1337=)
6g.7583069A>CCA362689453DSPc.4478A>C (p.Gln1493Pro)
c.5807A>C (p.Gln1936Pro)
c.4010A>C (p.Gln1337Pro)
6g.7583069A>GCA362689454DSPc.4478A>G (p.Gln1493Arg)
c.5807A>G (p.Gln1936Arg)
c.4010A>G (p.Gln1337Arg)
gnomAD v4
6g.7583069A>TCA362689455DSPc.4478A>T (p.Gln1493Leu)
c.5807A>T (p.Gln1936Leu)
c.4010A>T (p.Gln1337Leu)
ClinVar dbSNP gnomAD v4
6g.7583070G>ACA448715602DSPc.4479G>A (p.Gln1493=)
c.5808G>A (p.Gln1936=)
c.4011G>A (p.Gln1337=)
ClinVar
6g.7583070G>CCA045802DSPc.4479G>C (p.Gln1493His)
c.5808G>C (p.Gln1936His)
c.4011G>C (p.Gln1337His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
6g.7583070G=CA1608607118DSPc.4479G= (p.Gln1493=)
c.5808G= (p.Gln1936=)
c.4011G= (p.Gln1337=)
6g.7583070G>TCA362689456DSPc.4479G>T (p.Gln1493His)
c.5808G>T (p.Gln1936His)
c.4011G>T (p.Gln1337His)
6g.7583071A>CCA448715603DSPc.4480A>C (p.Arg1494=)
c.5809A>C (p.Arg1937=)
c.4012A>C (p.Arg1338=)
6g.7583071A>GCA362689457DSPc.4480A>G (p.Arg1494Gly)
c.5809A>G (p.Arg1937Gly)
c.4012A>G (p.Arg1338Gly)
6g.7583071A>TCA362689458DSPc.4480A>T (p.Arg1494Trp)
c.5809A>T (p.Arg1937Trp)
c.4012A>T (p.Arg1338Trp)
6g.7583072G>ACA045816DSPc.4481G>A (p.Arg1494Lys)
c.5810G>A (p.Arg1937Lys)
c.4013G>A (p.Arg1338Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7583072G>CCA362689459DSPc.4481G>C (p.Arg1494Thr)
c.5810G>C (p.Arg1937Thr)
c.4013G>C (p.Arg1338Thr)
6g.7583072G=CA1608607120DSPc.4481G= (p.Arg1494=)
c.5810G= (p.Arg1937=)
c.4013G= (p.Arg1338=)
6g.7583072G>TCA362689460DSPc.4481G>T (p.Arg1494Met)
c.5810G>T (p.Arg1937Met)
c.4013G>T (p.Arg1338Met)
6g.7583073G>ACA448715605DSPc.4482G>A (p.Arg1494=)
c.5811G>A (p.Arg1937=)
c.4014G>A (p.Arg1338=)
6g.7583073G>CCA362689461DSPc.4482G>C (p.Arg1494Ser)
c.5811G>C (p.Arg1937Ser)
c.4014G>C (p.Arg1338Ser)
6g.7583073G>TCA362689462DSPc.4482G>T (p.Arg1494Ser)
c.5811G>T (p.Arg1937Ser)
c.4014G>T (p.Arg1338Ser)
6g.7583074G>ACA362689463DSPc.4483G>A (p.Glu1495Lys)
c.5812G>A (p.Glu1938Lys)
c.4015G>A (p.Glu1339Lys)
COSMIC
6g.7583074G>CCA362689464DSPc.4483G>C (p.Glu1495Gln)
c.5812G>C (p.Glu1938Gln)
c.4015G>C (p.Glu1339Gln)
ClinVar
6g.7583074G>TCA362689465DSPc.4483G>T (p.Glu1495Ter)
c.5812G>T (p.Glu1938Ter)
c.4015G>T (p.Glu1339Ter)
6g.7583075A>CCA362689466DSPc.4484A>C (p.Glu1495Ala)
c.5813A>C (p.Glu1938Ala)
c.4016A>C (p.Glu1339Ala)
6g.7583075A>GCA362689467DSPc.4484A>G (p.Glu1495Gly)
c.5813A>G (p.Glu1938Gly)
c.4016A>G (p.Glu1339Gly)
6g.7583075A>TCA362689468DSPc.4484A>T (p.Glu1495Val)
c.5813A>T (p.Glu1938Val)
c.4016A>T (p.Glu1339Val)
6g.7583076G>ACA448715609DSPc.4485G>A (p.Glu1495=)
c.5814G>A (p.Glu1938=)
c.4017G>A (p.Glu1339=)
gnomAD v4
6g.7583076G>CCA362689470DSPc.4485G>C (p.Glu1495Asp)
c.5814G>C (p.Glu1938Asp)
c.4017G>C (p.Glu1339Asp)
6g.7583076G>TCA362689469DSPc.4485G>T (p.Glu1495Asp)
c.5814G>T (p.Glu1938Asp)
c.4017G>T (p.Glu1339Asp)
6g.7583077A>CCA362689471DSPc.4486A>C (p.Ile1496Leu)
c.5815A>C (p.Ile1939Leu)
c.4018A>C (p.Ile1340Leu)
6g.7583077A>GCA362689472DSPc.4486A>G (p.Ile1496Val)
c.5815A>G (p.Ile1939Val)
c.4018A>G (p.Ile1340Val)
6g.7583077A>TCA362689473DSPc.4486A>T (p.Ile1496Phe)
c.5815A>T (p.Ile1939Phe)
c.4018A>T (p.Ile1340Phe)
6g.7583078T>ACA362689474DSPc.4487T>A (p.Ile1496Asn)
c.5816T>A (p.Ile1939Asn)
c.4019T>A (p.Ile1340Asn)
6g.7583078T>CCA362689475DSPc.4487T>C (p.Ile1496Thr)
c.5816T>C (p.Ile1939Thr)
c.4019T>C (p.Ile1340Thr)
ClinVar
6g.7583078T>GCA362689476DSPc.4487T>G (p.Ile1496Ser)
c.5816T>G (p.Ile1939Ser)
c.4019T>G (p.Ile1340Ser)
6g.7583079T>ACA448715613DSPc.4488T>A (p.Ile1496=)
c.5817T>A (p.Ile1939=)
c.4020T>A (p.Ile1340=)
6g.7583079T>CCA448715615DSPc.4488T>C (p.Ile1496=)
c.5817T>C (p.Ile1939=)
c.4020T>C (p.Ile1340=)
dbSNP gnomAD v2 gnomAD v4
6g.7583079T>GCA362689477DSPc.4488T>G (p.Ile1496Met)
c.5817T>G (p.Ile1939Met)
c.4020T>G (p.Ile1340Met)
gnomAD v4
6g.7583079T=CA1608607128DSPc.4488T= (p.Ile1496=)
c.5817T= (p.Ile1939=)
c.4020T= (p.Ile1340=)
6g.7583080G>ACA362689478DSPc.4489G>A (p.Asp1497Asn)
c.5818G>A (p.Asp1940Asn)
c.4021G>A (p.Asp1341Asn)
COSMIC
6g.7583080G>CCA362689479DSPc.4489G>C (p.Asp1497His)
c.5818G>C (p.Asp1940His)
c.4021G>C (p.Asp1341His)
6g.7583080G>TCA362689480DSPc.4489G>T (p.Asp1497Tyr)
c.5818G>T (p.Asp1940Tyr)
c.4021G>T (p.Asp1341Tyr)
6g.7583081A=CA1608607134DSPc.4490A= (p.Asp1497=)
c.5819A= (p.Asp1940=)
c.4022A= (p.Asp1341=)
6g.7583081A>CCA362689481DSPc.4490A>C (p.Asp1497Ala)
c.5819A>C (p.Asp1940Ala)
c.4022A>C (p.Asp1341Ala)
6g.7583081A>GCA362689482DSPc.4490A>G (p.Asp1497Gly)
c.5819A>G (p.Asp1940Gly)
c.4022A>G (p.Asp1341Gly)
6g.7583081A>TCA362689483DSPc.4490A>T (p.Asp1497Val)
c.5819A>T (p.Asp1940Val)
c.4022A>T (p.Asp1341Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.7583082T>ACA362689485DSPc.4491T>A (p.Asp1497Glu)
c.5820T>A (p.Asp1940Glu)
c.4023T>A (p.Asp1341Glu)
6g.7583082T>CCA3628100DSPc.4491T>C (p.Asp1497=)
c.5820T>C (p.Asp1940=)
c.4023T>C (p.Asp1341=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
6g.7583082T>GCA362689484DSPc.4491T>G (p.Asp1497Glu)
c.5820T>G (p.Asp1940Glu)
c.4023T>G (p.Asp1341Glu)
6g.7583082T=CA1608607148DSPc.4491T= (p.Asp1497=)
c.5820T= (p.Asp1940=)
c.4023T= (p.Asp1341=)
6g.7583082_7583088delinsTAAACTCCA1608607153DSPc.4491_4497delinsTAAACTC (p.Asp1497=)
c.5820_5826delinsTAAACTC (p.Asp1940=)
c.4023_4029delinsTAAACTC (p.Asp1341=)
6g.7583083A=CA1608607166DSPc.4492A= (p.Lys1498=)
c.5821A= (p.Lys1941=)
c.4024A= (p.Lys1342=)
6g.7583083A>CCA362689486DSPc.4492A>C (p.Lys1498Gln)
c.5821A>C (p.Lys1941Gln)
c.4024A>C (p.Lys1342Gln)
6g.7583083A>GCA006629DSPc.4492A>G (p.Lys1498Glu)
c.5821A>G (p.Lys1941Glu)
c.4024A>G (p.Lys1342Glu)
ClinVar dbSNP
6g.7583083A>TCA362689487DSPc.4492A>T (p.Lys1498Ter)
c.5821A>T (p.Lys1941Ter)
c.4024A>T (p.Lys1342Ter)
6g.7583084_7583089delCA3628099DSPc.4493_4498del (p.Lys1498_Leu1499del)
c.5822_5827del (p.Lys1941_Leu1942del)
c.4025_4030del (p.Lys1342_Leu1343del)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.7583084A=CA1608607173DSPc.4493A= (p.Lys1498=)
c.5822A= (p.Lys1941=)
c.4025A= (p.Lys1342=)
6g.7583084A>CCA045860DSPc.4493A>C (p.Lys1498Thr)
c.5822A>C (p.Lys1941Thr)
c.4025A>C (p.Lys1342Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7583084A>GCA362689488DSPc.4493A>G (p.Lys1498Arg)
c.5822A>G (p.Lys1941Arg)
c.4025A>G (p.Lys1342Arg)
6g.7583084A>TCA362689489DSPc.4493A>T (p.Lys1498Ile)
c.5822A>T (p.Lys1941Ile)
c.4025A>T (p.Lys1342Ile)
6g.7583085A=CA1608607179DSPc.4494A= (p.Lys1498=)
c.5823A= (p.Lys1941=)
c.4026A= (p.Lys1342=)
6g.7583085A>CCA362689490DSPc.4494A>C (p.Lys1498Asn)
c.5823A>C (p.Lys1941Asn)
c.4026A>C (p.Lys1342Asn)
6g.7583085A>GCA133972444DSPc.4494A>G (p.Lys1498=)
c.5823A>G (p.Lys1941=)
c.4026A>G (p.Lys1342=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7583085A>TCA362689491DSPc.4494A>T (p.Lys1498Asn)
c.5823A>T (p.Lys1941Asn)
c.4026A>T (p.Lys1342Asn)
6g.7583086C>ACA362689492DSPc.4495C>A (p.Leu1499Ile)
c.5824C>A (p.Leu1942Ile)
c.4027C>A (p.Leu1343Ile)
6g.7583086C>GCA362689493DSPc.4495C>G (p.Leu1499Val)
c.5824C>G (p.Leu1942Val)
c.4027C>G (p.Leu1343Val)
6g.7583086C>TCA362689494DSPc.4495C>T (p.Leu1499Phe)
c.5824C>T (p.Leu1942Phe)
c.4027C>T (p.Leu1343Phe)
6g.7583087T>ACA362689495DSPc.4496T>A (p.Leu1499His)
c.5825T>A (p.Leu1942His)
c.4028T>A (p.Leu1343His)
6g.7583087T>CCA362689496DSPc.4496T>C (p.Leu1499Pro)
c.5825T>C (p.Leu1942Pro)
c.4028T>C (p.Leu1343Pro)
6g.7583087T>GCA362689497DSPc.4496T>G (p.Leu1499Arg)
c.5825T>G (p.Leu1942Arg)
c.4028T>G (p.Leu1343Arg)
6g.7583088C>ACA448715624DSPc.4497C>A (p.Leu1499=)
c.5826C>A (p.Leu1942=)
c.4029C>A (p.Leu1343=)
COSMIC
6g.7583088C>GCA448715623DSPc.4497C>G (p.Leu1499=)
c.5826C>G (p.Leu1942=)
c.4029C>G (p.Leu1343=)
6g.7583088C>TCA448715622DSPc.4497C>T (p.Leu1499=)
c.5826C>T (p.Leu1942=)
c.4029C>T (p.Leu1343=)
gnomAD v4
6g.7583091_7583094delCA2580075513DSPc.4500_4503del (p.Arg1500SerfsTer28)
c.5829_5832del (p.Arg1943SerfsTer28)
c.4032_4035del (p.Arg1344SerfsTer28)
ClinVar
6g.7583089A=CA1608607186DSPc.4498A= (p.Arg1500=)
c.5827A= (p.Arg1943=)
c.4030A= (p.Arg1344=)
6g.7583089A>CCA448715625DSPc.4498A>C (p.Arg1500=)
c.5827A>C (p.Arg1943=)
c.4030A>C (p.Arg1344=)
6g.7583089A>GCA006637DSPc.4498A>G (p.Arg1500Gly)
c.5827A>G (p.Arg1943Gly)
c.4030A>G (p.Arg1344Gly)
ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
6g.7583089A>TCA362689498DSPc.4498A>T (p.Arg1500Ter)
c.5827A>T (p.Arg1943Ter)
c.4030A>T (p.Arg1344Ter)
6g.7583090G>ACA362689499DSPc.4499G>A (p.Arg1500Lys)
c.5828G>A (p.Arg1943Lys)
c.4031G>A (p.Arg1344Lys)
dbSNP gnomAD v3 gnomAD v4 COSMIC
6g.7583090G>CCA362689501DSPc.4499G>C (p.Arg1500Thr)
c.5828G>C (p.Arg1943Thr)
c.4031G>C (p.Arg1344Thr)
6g.7583090G=CA1608607190DSPc.4499G= (p.Arg1500=)
c.5828G= (p.Arg1943=)
c.4031G= (p.Arg1344=)
6g.7583090G>TCA362689500DSPc.4499G>T (p.Arg1500Ile)
c.5828G>T (p.Arg1943Ile)
c.4031G>T (p.Arg1344Ile)
ClinVar
6g.7583091A>CCA362689502DSPc.4500A>C (p.Arg1500Ser)
c.5829A>C (p.Arg1943Ser)
c.4032A>C (p.Arg1344Ser)
6g.7583091A>GCA448715629DSPc.4500A>G (p.Arg1500=)
c.5829A>G (p.Arg1943=)
c.4032A>G (p.Arg1344=)
6g.7583091A>TCA362689503DSPc.4500A>T (p.Arg1500Ser)
c.5829A>T (p.Arg1943Ser)
c.4032A>T (p.Arg1344Ser)
6g.7583092C>ACA362689504DSPc.4501C>A (p.Gln1501Lys)
c.5830C>A (p.Gln1944Lys)
c.4033C>A (p.Gln1345Lys)
6g.7583092C>GCA362689505DSPc.4501C>G (p.Gln1501Glu)
c.5830C>G (p.Gln1944Glu)
c.4033C>G (p.Gln1345Glu)
6g.7583092C>TCA362689506DSPc.4501C>T (p.Gln1501Ter)
c.5830C>T (p.Gln1944Ter)
c.4033C>T (p.Gln1345Ter)
ClinVar dbSNP
6g.7583093A>CCA362689507DSPc.4502A>C (p.Gln1501Pro)
c.5831A>C (p.Gln1944Pro)
c.4034A>C (p.Gln1345Pro)
6g.7583093A>GCA362689508DSPc.4502A>G (p.Gln1501Arg)
c.5831A>G (p.Gln1944Arg)
c.4034A>G (p.Gln1345Arg)
6g.7583093A>TCA362689509DSPc.4502A>T (p.Gln1501Leu)
c.5831A>T (p.Gln1944Leu)
c.4034A>T (p.Gln1345Leu)
6g.7583094G>ACA448715631DSPc.4503G>A (p.Gln1501=)
c.5832G>A (p.Gln1944=)
c.4035G>A (p.Gln1345=)
6g.7583094G>CCA362689510DSPc.4503G>C (p.Gln1501His)
c.5832G>C (p.Gln1944His)
c.4035G>C (p.Gln1345His)
6g.7583094G>TCA362689511DSPc.4503G>T (p.Gln1501His)
c.5832G>T (p.Gln1944His)
c.4035G>T (p.Gln1345His)
6g.7583095C>ACA362689513DSPc.4504C>A (p.Arg1502Ser)
c.5833C>A (p.Arg1945Ser)
c.4036C>A (p.Arg1346Ser)
6g.7583095C=CA1608607196DSPc.4504C= (p.Arg1502=)
c.5833C= (p.Arg1945=)
c.4036C= (p.Arg1346=)
6g.7583095C>GCA362689514DSPc.4504C>G (p.Arg1502Gly)
c.5833C>G (p.Arg1945Gly)
c.4036C>G (p.Arg1346Gly)
6g.7583095C>TCA362689512DSPc.4504C>T (p.Arg1502Cys)
c.5833C>T (p.Arg1945Cys)
c.4036C>T (p.Arg1346Cys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7583096G>ACA045886DSPc.4505G>A (p.Arg1502His)
c.5834G>A (p.Arg1945His)
c.4037G>A (p.Arg1346His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
6g.7583096G>CCA362689515DSPc.4505G>C (p.Arg1502Pro)
c.5834G>C (p.Arg1945Pro)
c.4037G>C (p.Arg1346Pro)
6g.7583096G=CA1608607203DSPc.4505G= (p.Arg1502=)
c.5834G= (p.Arg1945=)
c.4037G= (p.Arg1346=)
6g.7583096G>TCA362689516DSPc.4505G>T (p.Arg1502Leu)
c.5834G>T (p.Arg1945Leu)
c.4037G>T (p.Arg1346Leu)
gnomAD v4
6g.7583097C>ACA448715636DSPc.4506C>A (p.Arg1502=)
c.5835C>A (p.Arg1945=)
c.4038C>A (p.Arg1346=)
6g.7583097C=CA1608607214DSPc.4506C= (p.Arg1502=)
c.5835C= (p.Arg1945=)
c.4038C= (p.Arg1346=)
6g.7583097C>GCA448715637DSPc.4506C>G (p.Arg1502=)
c.5835C>G (p.Arg1945=)
c.4038C>G (p.Arg1346=)
6g.7583097C>TCA448715638DSPc.4506C>T (p.Arg1502=)
c.5835C>T (p.Arg1945=)
c.4038C>T (p.Arg1346=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7583098C>ACA362689517DSPc.4507C>A (p.Pro1503Thr)
c.5836C>A (p.Pro1946Thr)
c.4039C>A (p.Pro1347Thr)
COSMIC
6g.7583098C=CA1608607227DSPc.4507C= (p.Pro1503=)
c.5836C= (p.Pro1946=)
c.4039C= (p.Pro1347=)
6g.7583098C>GCA362689518DSPc.4507C>G (p.Pro1503Ala)
c.5836C>G (p.Pro1946Ala)
c.4039C>G (p.Pro1347Ala)
6g.7583098C>TCA133972481DSPc.4507C>T (p.Pro1503Ser)
c.5836C>T (p.Pro1946Ser)
c.4039C>T (p.Pro1347Ser)
dbSNP gnomAD v4
6g.7583099C>ACA362689521DSPc.4508C>A (p.Pro1503Gln)
c.5837C>A (p.Pro1946Gln)
c.4040C>A (p.Pro1347Gln)
6g.7583099C=CA1608607232DSPc.4508C= (p.Pro1503=)
c.5837C= (p.Pro1946=)
c.4040C= (p.Pro1347=)
6g.7583099C>GCA362689519DSPc.4508C>G (p.Pro1503Arg)
c.5837C>G (p.Pro1946Arg)
c.4040C>G (p.Pro1347Arg)
6g.7583099C>TCA362689520DSPc.4508C>T (p.Pro1503Leu)
c.5837C>T (p.Pro1946Leu)
c.4040C>T (p.Pro1347Leu)
ClinVar gnomAD v4
6g.7583100A=CA1608607236DSPc.4509A= (p.Pro1503=)
c.5838A= (p.Pro1946=)
c.4041A= (p.Pro1347=)
6g.7583100A>CCA133972545DSPc.4509A>C (p.Pro1503=)
c.5838A>C (p.Pro1946=)
c.4041A>C (p.Pro1347=)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.7583100A>GCA448715641DSPc.4509A>G (p.Pro1503=)
c.5838A>G (p.Pro1946=)
c.4041A>G (p.Pro1347=)
ClinVar
6g.7583100A>TCA448715639DSPc.4509A>T (p.Pro1503=)
c.5838A>T (p.Pro1946=)
c.4041A>T (p.Pro1347=)
6g.7583102_7583103dupCA133972518DSPc.4511_4512dup (p.Gly1505MetfsTer25)
c.5840_5841dup (p.Gly1948MetfsTer25)
c.4043_4044dup (p.Gly1349MetfsTer25)
ClinVar dbSNP
6g.7583101T>ACA362689522DSPc.4510T>A (p.Tyr1504Asn)
c.5839T>A (p.Tyr1947Asn)
c.4042T>A (p.Tyr1348Asn)
6g.7583101T>CCA045899DSPc.4510T>C (p.Tyr1504His)
c.5839T>C (p.Tyr1947His)
c.4042T>C (p.Tyr1348His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7583101T>GCA362689523DSPc.4510T>G (p.Tyr1504Asp)
c.5839T>G (p.Tyr1947Asp)
c.4042T>G (p.Tyr1348Asp)
6g.7583101T=CA1608607240DSPc.4510T= (p.Tyr1504=)
c.5839T= (p.Tyr1947=)
c.4042T= (p.Tyr1348=)
6g.7583102A=CA1608607247DSPc.4511A= (p.Tyr1504=)
c.5840A= (p.Tyr1947=)
c.4043A= (p.Tyr1348=)
6g.7583102A>CCA362689524DSPc.4511A>C (p.Tyr1504Ser)
c.5840A>C (p.Tyr1947Ser)
c.4043A>C (p.Tyr1348Ser)
6g.7583102A>GCA362689526DSPc.4511A>G (p.Tyr1504Cys)
c.5840A>G (p.Tyr1947Cys)
c.4043A>G (p.Tyr1348Cys)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.7583102A>TCA362689525DSPc.4511A>T (p.Tyr1504Phe)
c.5840A>T (p.Tyr1947Phe)
c.4043A>T (p.Tyr1348Phe)
6g.7583103T>ACA362689527DSPc.4512T>A (p.Tyr1504Ter)
c.5841T>A (p.Tyr1947Ter)
c.4044T>A (p.Tyr1348Ter)
6g.7583103T>CCA448715644DSPc.4512T>C (p.Tyr1504=)
c.5841T>C (p.Tyr1947=)
c.4044T>C (p.Tyr1348=)
gnomAD v4
6g.7583103T>GCA362689528DSPc.4512T>G (p.Tyr1504Ter)
c.5841T>G (p.Tyr1947Ter)
c.4044T>G (p.Tyr1348Ter)
6g.7583104G>ACA362689529DSPc.4513G>A (p.Gly1505Arg)
c.5842G>A (p.Gly1948Arg)
c.4045G>A (p.Gly1349Arg)
6g.7583104G>CCA362689530DSPc.4513G>C (p.Gly1505Arg)
c.5842G>C (p.Gly1948Arg)
c.4045G>C (p.Gly1349Arg)
6g.7583104G>TCA362689531DSPc.4513G>T (p.Gly1505Trp)
c.5842G>T (p.Gly1948Trp)
c.4045G>T (p.Gly1349Trp)
gnomAD v4
6g.7583105G>ACA362689532DSPc.4514G>A (p.Gly1505Glu)
c.5843G>A (p.Gly1948Glu)
c.4046G>A (p.Gly1349Glu)
6g.7583105G>CCA362689533DSPc.4514G>C (p.Gly1505Ala)
c.5843G>C (p.Gly1948Ala)
c.4046G>C (p.Gly1349Ala)
6g.7583105G>TCA362689534DSPc.4514G>T (p.Gly1505Val)
c.5843G>T (p.Gly1948Val)
c.4046G>T (p.Gly1349Val)
6g.7583106G>ACA448715648DSPc.4515G>A (p.Gly1505=)
c.5844G>A (p.Gly1948=)
c.4047G>A (p.Gly1349=)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.7583106G>CCA448715649DSPc.4515G>C (p.Gly1505=)
c.5844G>C (p.Gly1948=)
c.4047G>C (p.Gly1349=)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.7583106G=CA1608607253DSPc.4515G= (p.Gly1505=)
c.5844G= (p.Gly1948=)
c.4047G= (p.Gly1349=)
6g.7583106G>TCA448715650DSPc.4515G>T (p.Gly1505=)
c.5844G>T (p.Gly1948=)
c.4047G>T (p.Gly1349=)
6g.7583107T>ACA362689535DSPc.4516T>A (p.Ser1506Thr)
c.5845T>A (p.Ser1949Thr)
c.4048T>A (p.Ser1350Thr)
6g.7583107T>CCA362689536DSPc.4516T>C (p.Ser1506Pro)
c.5845T>C (p.Ser1949Pro)
c.4048T>C (p.Ser1350Pro)
6g.7583107T>GCA362689537DSPc.4516T>G (p.Ser1506Ala)
c.5845T>G (p.Ser1949Ala)
c.4048T>G (p.Ser1350Ala)
6g.7583108C>ACA362689539DSPc.4517C>A (p.Ser1506Tyr)
c.5846C>A (p.Ser1949Tyr)
c.4049C>A (p.Ser1350Tyr)
6g.7583108C=CA1608607258DSPc.4517C= (p.Ser1506=)
c.5846C= (p.Ser1949=)
c.4049C= (p.Ser1350=)
6g.7583108C>GCA362689538DSPc.4517C>G (p.Ser1506Cys)
c.5846C>G (p.Ser1949Cys)
c.4049C>G (p.Ser1350Cys)
6g.7583108C>TCA16605158DSPc.4517C>T (p.Ser1506Phe)
c.5846C>T (p.Ser1949Phe)
c.4049C>T (p.Ser1350Phe)
ClinVar dbSNP COSMIC
6g.7583109C>ACA133972561DSPc.4518C>A (p.Ser1506=)
c.5847C>A (p.Ser1949=)
c.4050C>A (p.Ser1350=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7583109C=CA1608607276DSPc.4518C= (p.Ser1506=)
c.5847C= (p.Ser1949=)
c.4050C= (p.Ser1350=)
6g.7583109C>GCA448715651DSPc.4518C>G (p.Ser1506=)
c.5847C>G (p.Ser1949=)
c.4050C>G (p.Ser1350=)
6g.7583109C>TCA448715653DSPc.4518C>T (p.Ser1506=)
c.5847C>T (p.Ser1949=)
c.4050C>T (p.Ser1350=)
6g.7583110C>ACA362689540DSPc.4519C>A (p.His1507Asn)
c.5848C>A (p.His1950Asn)
c.4051C>A (p.His1351Asn)
6g.7583110C>GCA362689542DSPc.4519C>G (p.His1507Asp)
c.5848C>G (p.His1950Asp)
c.4051C>G (p.His1351Asp)
6g.7583110C>TCA362689541DSPc.4519C>T (p.His1507Tyr)
c.5848C>T (p.His1950Tyr)
c.4051C>T (p.His1351Tyr)
6g.7583111A>CCA362689543DSPc.4520A>C (p.His1507Pro)
c.5849A>C (p.His1950Pro)
c.4052A>C (p.His1351Pro)
6g.7583111A>GCA362689544DSPc.4520A>G (p.His1507Arg)
c.5849A>G (p.His1950Arg)
c.4052A>G (p.His1351Arg)
gnomAD v4
6g.7583111A>TCA362689545DSPc.4520A>T (p.His1507Leu)
c.5849A>T (p.His1950Leu)
c.4052A>T (p.His1351Leu)
6g.7583112T>ACA362689546DSPc.4521T>A (p.His1507Gln)
c.5850T>A (p.His1950Gln)
c.4053T>A (p.His1351Gln)
6g.7583112T>CCA448715655DSPc.4521T>C (p.His1507=)
c.5850T>C (p.His1950=)
c.4053T>C (p.His1351=)
6g.7583112T>GCA362689547DSPc.4521T>G (p.His1507Gln)
c.5850T>G (p.His1950Gln)
c.4053T>G (p.His1351Gln)
6g.7583112_7583113delinsATCA2573140811DSPc.4521_4522delinsAT (p.His1507GlnfsTer2)
c.5850_5851delinsAT (p.His1950GlnfsTer2)
c.4053_4054delinsAT (p.His1351GlnfsTer2)
ClinVar dbSNP
6g.7583113C>ACA448715656DSPc.4522C>A (p.Arg1508=)
c.5851C>A (p.Arg1951=)
c.4054C>A (p.Arg1352=)
6g.7583113C=CA1608607285DSPc.4522C= (p.Arg1508=)
c.5851C= (p.Arg1951=)
c.4054C= (p.Arg1352=)
6g.7583113C>GCA362689548DSPc.4522C>G (p.Arg1508Gly)
c.5851C>G (p.Arg1951Gly)
c.4054C>G (p.Arg1352Gly)
ClinVar dbSNP
6g.7583113C>TCA353961DSPc.4522C>T (p.Arg1508Ter)
c.5851C>T (p.Arg1951Ter)
c.4054C>T (p.Arg1352Ter)
ClinVar dbSNP gnomAD v4
6g.7583114G>ACA362689549DSPc.4523G>A (p.Arg1508Gln)
c.5852G>A (p.Arg1951Gln)
c.4055G>A (p.Arg1352Gln)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7583114G>CCA362689550DSPc.4523G>C (p.Arg1508Pro)
c.5852G>C (p.Arg1951Pro)
c.4055G>C (p.Arg1352Pro)
gnomAD v4
6g.7583114G=CA1608607292DSPc.4523G= (p.Arg1508=)
c.5852G= (p.Arg1951=)
c.4055G= (p.Arg1352=)
6g.7583114G>TCA362689551DSPc.4523G>T (p.Arg1508Leu)
c.5852G>T (p.Arg1951Leu)
c.4055G>T (p.Arg1352Leu)
6g.7583118_7583119delCA2710966108DSPc.4527_4528del (p.Glu1509AspfsTer4)
c.5856_5857del (p.Glu1952AspfsTer4)
c.4059_4060del (p.Glu1353AspfsTer4)
dbSNP
6g.7583115A>CCA448715661DSPc.4524A>C (p.Arg1508=)
c.5853A>C (p.Arg1951=)
c.4056A>C (p.Arg1352=)
6g.7583115A>GCA448715660DSPc.4524A>G (p.Arg1508=)
c.5853A>G (p.Arg1951=)
c.4056A>G (p.Arg1352=)
6g.7583115A>TCA448715658DSPc.4524A>T (p.Arg1508=)
c.5853A>T (p.Arg1951=)
c.4056A>T (p.Arg1352=)
6g.7583116G>ACA362689554DSPc.4525G>A (p.Glu1509Lys)
c.5854G>A (p.Glu1952Lys)
c.4057G>A (p.Glu1353Lys)
6g.7583116G>CCA362689553DSPc.4525G>C (p.Glu1509Gln)
c.5854G>C (p.Glu1952Gln)
c.4057G>C (p.Glu1353Gln)
6g.7583116G>TCA362689552DSPc.4525G>T (p.Glu1509Ter)
c.5854G>T (p.Glu1952Ter)
c.4057G>T (p.Glu1353Ter)
6g.7583116_7583117delinsGACA1608607299DSPc.4525_4526delinsGA (p.Glu1509=)
c.5854_5855delinsGA (p.Glu1952=)
c.4057_4058delinsGA (p.Glu1353=)
6g.7583117delCA1139659418DSPc.4526del (p.Glu1509GlyfsTer20)
c.5855del (p.Glu1952GlyfsTer20)
c.4058del (p.Glu1353GlyfsTer20)
ClinVar dbSNP
6g.7583117A>CCA362689555DSPc.4526A>C (p.Glu1509Ala)
c.5855A>C (p.Glu1952Ala)
c.4058A>C (p.Glu1353Ala)
6g.7583117A>GCA362689556DSPc.4526A>G (p.Glu1509Gly)
c.5855A>G (p.Glu1952Gly)
c.4058A>G (p.Glu1353Gly)
6g.7583117A>TCA362689557DSPc.4526A>T (p.Glu1509Val)
c.5855A>T (p.Glu1952Val)
c.4058A>T (p.Glu1353Val)
6g.7583118G>ACA448715662DSPc.4527G>A (p.Glu1509=)
c.5856G>A (p.Glu1952=)
c.4059G>A (p.Glu1353=)
6g.7583118G>CCA362689558DSPc.4527G>C (p.Glu1509Asp)
c.5856G>C (p.Glu1952Asp)
c.4059G>C (p.Glu1353Asp)
6g.7583118G>TCA362689559DSPc.4527G>T (p.Glu1509Asp)
c.5856G>T (p.Glu1952Asp)
c.4059G>T (p.Glu1353Asp)
gnomAD v4
6g.7583122_7583142delCA2677235160DSPc.4531_4551del (p.Gln1511_Thr1517del)
c.5860_5880del (p.Gln1954_Thr1960del)
c.4063_4083del (p.Gln1355_Thr1361del)
gnomAD v4
6g.7583119A>CCA362689560DSPc.4528A>C (p.Thr1510Pro)
c.5857A>C (p.Thr1953Pro)
c.4060A>C (p.Thr1354Pro)
6g.7583119A>GCA362689561DSPc.4528A>G (p.Thr1510Ala)
c.5857A>G (p.Thr1953Ala)
c.4060A>G (p.Thr1354Ala)
6g.7583119A>TCA362689562DSPc.4528A>T (p.Thr1510Ser)
c.5857A>T (p.Thr1953Ser)
c.4060A>T (p.Thr1354Ser)
6g.7583120C>ACA362689563DSPc.4529C>A (p.Thr1510Asn)
c.5858C>A (p.Thr1953Asn)
c.4061C>A (p.Thr1354Asn)
6g.7583120C>GCA362689564DSPc.4529C>G (p.Thr1510Ser)
c.5858C>G (p.Thr1953Ser)
c.4061C>G (p.Thr1354Ser)
6g.7583120C>TCA362689565DSPc.4529C>T (p.Thr1510Ile)
c.5858C>T (p.Thr1953Ile)
c.4061C>T (p.Thr1354Ile)
6g.7583121C>ACA448715666DSPc.4530C>A (p.Thr1510=)
c.5859C>A (p.Thr1953=)
c.4062C>A (p.Thr1354=)
COSMIC
6g.7583121C=CA1608607311DSPc.4530C= (p.Thr1510=)
c.5859C= (p.Thr1953=)
c.4062C= (p.Thr1354=)
6g.7583121C>GCA045924DSPc.4530C>G (p.Thr1510=)
c.5859C>G (p.Thr1953=)
c.4062C>G (p.Thr1354=)
ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
6g.7583121C>TCA448715667DSPc.4530C>T (p.Thr1510=)
c.5859C>T (p.Thr1953=)
c.4062C>T (p.Thr1354=)
ClinVar dbSNP gnomAD v4
6g.7583122C>ACA362689567DSPc.4531C>A (p.Gln1511Lys)
c.5860C>A (p.Gln1954Lys)
c.4063C>A (p.Gln1355Lys)
6g.7583122C>GCA362689568DSPc.4531C>G (p.Gln1511Glu)
c.5860C>G (p.Gln1954Glu)
c.4063C>G (p.Gln1355Glu)
6g.7583122C>TCA362689566DSPc.4531C>T (p.Gln1511Ter)
c.5860C>T (p.Gln1954Ter)
c.4063C>T (p.Gln1355Ter)
6g.7583123A>CCA362689569DSPc.4532A>C (p.Gln1511Pro)
c.5861A>C (p.Gln1954Pro)
c.4064A>C (p.Gln1355Pro)
gnomAD v4
6g.7583123A>GCA362689570DSPc.4532A>G (p.Gln1511Arg)
c.5861A>G (p.Gln1954Arg)
c.4064A>G (p.Gln1355Arg)
6g.7583123A>TCA362689571DSPc.4532A>T (p.Gln1511Leu)
c.5861A>T (p.Gln1954Leu)
c.4064A>T (p.Gln1355Leu)
6g.7583124G>ACA448715668DSPc.4533G>A (p.Gln1511=)
c.5862G>A (p.Gln1954=)
c.4065G>A (p.Gln1355=)
6g.7583124G>CCA362689572DSPc.4533G>C (p.Gln1511His)
c.5862G>C (p.Gln1954His)
c.4065G>C (p.Gln1355His)
dbSNP gnomAD v4
6g.7583124G=CA1608607314DSPc.4533G= (p.Gln1511=)
c.5862G= (p.Gln1954=)
c.4065G= (p.Gln1355=)
6g.7583124G>TCA362689573DSPc.4533G>T (p.Gln1511His)
c.5862G>T (p.Gln1954His)
c.4065G>T (p.Gln1355His)
gnomAD v4
6g.7583125A>CCA362689576DSPc.4534A>C (p.Thr1512Pro)
c.5863A>C (p.Thr1955Pro)
c.4066A>C (p.Thr1356Pro)
6g.7583125A>GCA362689575DSPc.4534A>G (p.Thr1512Ala)
c.5863A>G (p.Thr1955Ala)
c.4066A>G (p.Thr1356Ala)
6g.7583125A>TCA362689574DSPc.4534A>T (p.Thr1512Ser)
c.5863A>T (p.Thr1955Ser)
c.4066A>T (p.Thr1356Ser)
6g.7583126C>ACA362689577DSPc.4535C>A (p.Thr1512Asn)
c.5864C>A (p.Thr1955Asn)
c.4067C>A (p.Thr1356Asn)
6g.7583126C=CA1608607318DSPc.4535C= (p.Thr1512=)
c.5864C= (p.Thr1955=)
c.4067C= (p.Thr1356=)
6g.7583126C>GCA362689578DSPc.4535C>G (p.Thr1512Ser)
c.5864C>G (p.Thr1955Ser)
c.4067C>G (p.Thr1356Ser)
6g.7583126C>TCA045944DSPc.4535C>T (p.Thr1512Ile)
c.5864C>T (p.Thr1955Ile)
c.4067C>T (p.Thr1356Ile)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.7583127T>ACA448715670DSPc.4536T>A (p.Thr1512=)
c.5865T>A (p.Thr1955=)
c.4068T>A (p.Thr1356=)
6g.7583127T>CCA448715671DSPc.4536T>C (p.Thr1512=)
c.5865T>C (p.Thr1955=)
c.4068T>C (p.Thr1356=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7583127T>GCA448715672DSPc.4536T>G (p.Thr1512=)
c.5865T>G (p.Thr1955=)
c.4068T>G (p.Thr1356=)
6g.7583127T=CA1608607325DSPc.4536T= (p.Thr1512=)
c.5865T= (p.Thr1955=)
c.4068T= (p.Thr1356=)
6g.7583128G>ACA362689579DSPc.4537G>A (p.Glu1513Lys)
c.5866G>A (p.Glu1956Lys)
c.4069G>A (p.Glu1357Lys)
ClinVar dbSNP
6g.7583128G>CCA362689580DSPc.4537G>C (p.Glu1513Gln)
c.5866G>C (p.Glu1956Gln)
c.4069G>C (p.Glu1357Gln)
6g.7583128G=CA1608607332DSPc.4537G= (p.Glu1513=)
c.5866G= (p.Glu1956=)
c.4069G= (p.Glu1357=)
6g.7583128G>TCA362689581DSPc.4537G>T (p.Glu1513Ter)
c.5866G>T (p.Glu1956Ter)
c.4069G>T (p.Glu1357Ter)
6g.7583129A>CCA362689582DSPc.4538A>C (p.Glu1513Ala)
c.5867A>C (p.Glu1956Ala)
c.4070A>C (p.Glu1357Ala)
6g.7583129A>GCA362689584DSPc.4538A>G (p.Glu1513Gly)
c.5867A>G (p.Glu1956Gly)
c.4070A>G (p.Glu1357Gly)
6g.7583129A>TCA362689583DSPc.4538A>T (p.Glu1513Val)
c.5867A>T (p.Glu1956Val)
c.4070A>T (p.Glu1357Val)
6g.7583130G>ACA448715674DSPc.4539G>A (p.Glu1513=)
c.5868G>A (p.Glu1956=)
c.4071G>A (p.Glu1357=)
6g.7583130G>CCA362689585DSPc.4539G>C (p.Glu1513Asp)
c.5868G>C (p.Glu1956Asp)
c.4071G>C (p.Glu1357Asp)
dbSNP
6g.7583130G>TCA362689586DSPc.4539G>T (p.Glu1513Asp)
c.5868G>T (p.Glu1956Asp)
c.4071G>T (p.Glu1357Asp)
6g.7583131T>ACA362689587DSPc.4540T>A (p.Cys1514Ser)
c.5869T>A (p.Cys1957Ser)
c.4072T>A (p.Cys1358Ser)
gnomAD v3 gnomAD v4
6g.7583131T>CCA362689588DSPc.4540T>C (p.Cys1514Arg)
c.5869T>C (p.Cys1957Arg)
c.4072T>C (p.Cys1358Arg)
ClinVar dbSNP
6g.7583131T>GCA362689589DSPc.4540T>G (p.Cys1514Gly)
c.5869T>G (p.Cys1957Gly)
c.4072T>G (p.Cys1358Gly)
6g.7583132G>ACA362689590DSPc.4541G>A (p.Cys1514Tyr)
c.5870G>A (p.Cys1957Tyr)
c.4073G>A (p.Cys1358Tyr)
6g.7583132G>CCA362689591DSPc.4541G>C (p.Cys1514Ser)
c.5870G>C (p.Cys1957Ser)
c.4073G>C (p.Cys1358Ser)
6g.7583132G>TCA362689592DSPc.4541G>T (p.Cys1514Phe)
c.5870G>T (p.Cys1957Phe)
c.4073G>T (p.Cys1358Phe)
6g.7583133T>ACA362689593DSPc.4542T>A (p.Cys1514Ter)
c.5871T>A (p.Cys1957Ter)
c.4074T>A (p.Cys1358Ter)
6g.7583133T>CCA448715677DSPc.4542T>C (p.Cys1514=)
c.5871T>C (p.Cys1957=)
c.4074T>C (p.Cys1358=)
6g.7583133T>GCA362689594DSPc.4542T>G (p.Cys1514Trp)
c.5871T>G (p.Cys1957Trp)
c.4074T>G (p.Cys1358Trp)
6g.7583134G>ACA362689595DSPc.4543G>A (p.Glu1515Lys)
c.5872G>A (p.Glu1958Lys)
c.4075G>A (p.Glu1359Lys)
6g.7583134G>CCA362689596DSPc.4543G>C (p.Glu1515Gln)
c.5872G>C (p.Glu1958Gln)
c.4075G>C (p.Glu1359Gln)
dbSNP gnomAD v4
6g.7583134G=CA1608607338DSPc.4543G= (p.Glu1515=)
c.5872G= (p.Glu1958=)
c.4075G= (p.Glu1359=)
6g.7583134G>TCA362689597DSPc.4543G>T (p.Glu1515Ter)
c.5872G>T (p.Glu1958Ter)
c.4075G>T (p.Glu1359Ter)
6g.7583135A>CCA362689599DSPc.4544A>C (p.Glu1515Ala)
c.5873A>C (p.Glu1958Ala)
c.4076A>C (p.Glu1359Ala)
6g.7583135A>GCA362689600DSPc.4544A>G (p.Glu1515Gly)
c.5873A>G (p.Glu1958Gly)
c.4076A>G (p.Glu1359Gly)
6g.7583135A>TCA362689598DSPc.4544A>T (p.Glu1515Val)
c.5873A>T (p.Glu1958Val)
c.4076A>T (p.Glu1359Val)
6g.7583136G>ACA448715681DSPc.4545G>A (p.Glu1515=)
c.5874G>A (p.Glu1958=)
c.4077G>A (p.Glu1359=)
6g.7583136G>CCA362689601DSPc.4545G>C (p.Glu1515Asp)
c.5874G>C (p.Glu1958Asp)
c.4077G>C (p.Glu1359Asp)
ClinVar
6g.7583136G>TCA362689602DSPc.4545G>T (p.Glu1515Asp)
c.5874G>T (p.Glu1958Asp)
c.4077G>T (p.Glu1359Asp)
6g.7583137T>ACA362689603DSPc.4546T>A (p.Trp1516Arg)
c.5875T>A (p.Trp1959Arg)
c.4078T>A (p.Trp1360Arg)
6g.7583137T>CCA362689605DSPc.4546T>C (p.Trp1516Arg)
c.5875T>C (p.Trp1959Arg)
c.4078T>C (p.Trp1360Arg)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.7583137T>GCA362689604DSPc.4546T>G (p.Trp1516Gly)
c.5875T>G (p.Trp1959Gly)
c.4078T>G (p.Trp1360Gly)
6g.7583137T=CA1608607342DSPc.4546T= (p.Trp1516=)
c.5875T= (p.Trp1959=)
c.4078T= (p.Trp1360=)
6g.7583138G>ACA362689606DSPc.4547G>A (p.Trp1516Ter)
c.5876G>A (p.Trp1959Ter)
c.4079G>A (p.Trp1360Ter)
6g.7583138G>CCA362689607DSPc.4547G>C (p.Trp1516Ser)
c.5876G>C (p.Trp1959Ser)
c.4079G>C (p.Trp1360Ser)
6g.7583138G>TCA362689608DSPc.4547G>T (p.Trp1516Leu)
c.5876G>T (p.Trp1959Leu)
c.4079G>T (p.Trp1360Leu)
6g.7583139G>ACA133972604DSPc.4548G>A (p.Trp1516Ter)
c.5877G>A (p.Trp1959Ter)
c.4080G>A (p.Trp1360Ter)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.7583139G>CCA362689609DSPc.4548G>C (p.Trp1516Cys)
c.5877G>C (p.Trp1959Cys)
c.4080G>C (p.Trp1360Cys)
6g.7583139G=CA1608607345DSPc.4548G= (p.Trp1516=)
c.5877G= (p.Trp1959=)
c.4080G= (p.Trp1360=)
6g.7583139G>TCA362689610DSPc.4548G>T (p.Trp1516Cys)
c.5877G>T (p.Trp1959Cys)
c.4080G>T (p.Trp1360Cys)
6g.7583140A=CA1608607350DSPc.4549A= (p.Thr1517=)
c.5878A= (p.Thr1960=)
c.4081A= (p.Thr1361=)
6g.7583140A>CCA362689611DSPc.4549A>C (p.Thr1517Pro)
c.5878A>C (p.Thr1960Pro)
c.4081A>C (p.Thr1361Pro)
dbSNP gnomAD v4
6g.7583140A>GCA362689612DSPc.4549A>G (p.Thr1517Ala)
c.5878A>G (p.Thr1960Ala)
c.4081A>G (p.Thr1361Ala)
6g.7583140A>TCA362689613DSPc.4549A>T (p.Thr1517Ser)
c.5878A>T (p.Thr1960Ser)
c.4081A>T (p.Thr1361Ser)
6g.7583141C>ACA362689614DSPc.4550C>A (p.Thr1517Asn)
c.5879C>A (p.Thr1960Asn)
c.4082C>A (p.Thr1361Asn)
6g.7583141C=CA1608607356DSPc.4550C= (p.Thr1517=)
c.5879C= (p.Thr1960=)
c.4082C= (p.Thr1361=)
6g.7583141C>GCA362689615DSPc.4550C>G (p.Thr1517Ser)
c.5879C>G (p.Thr1960Ser)
c.4082C>G (p.Thr1361Ser)
6g.7583141C>TCA362689616DSPc.4550C>T (p.Thr1517Ile)
c.5879C>T (p.Thr1960Ile)
c.4082C>T (p.Thr1361Ile)
dbSNP
6g.7583142C>ACA448715685DSPc.4551C>A (p.Thr1517=)
c.5880C>A (p.Thr1960=)
c.4083C>A (p.Thr1361=)
6g.7583142C=CA1608607360DSPc.4551C= (p.Thr1517=)
c.5880C= (p.Thr1960=)
c.4083C= (p.Thr1361=)
6g.7583142C>GCA448715686DSPc.4551C>G (p.Thr1517=)
c.5880C>G (p.Thr1960=)
c.4083C>G (p.Thr1361=)
6g.7583142C>TCA045967DSPc.4551C>T (p.Thr1517=)
c.5880C>T (p.Thr1960=)
c.4083C>T (p.Thr1361=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
6g.7583143G>ACA006646DSPc.4552G>A (p.Val1518Ile)
c.5881G>A (p.Val1961Ile)
c.4084G>A (p.Val1362Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7583143G>CCA362689618DSPc.4552G>C (p.Val1518Leu)
c.5881G>C (p.Val1961Leu)
c.4084G>C (p.Val1362Leu)
gnomAD v4
6g.7583143G=CA1608607371DSPc.4552G= (p.Val1518=)
c.5881G= (p.Val1961=)
c.4084G= (p.Val1362=)
6g.7583143G>TCA362689617DSPc.4552G>T (p.Val1518Phe)
c.5881G>T (p.Val1961Phe)
c.4084G>T (p.Val1362Phe)

Number of alleles fetched