Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.76346080_76346095delCA2831039014BBS10c.1890_1905del (p.Ser630ArgfsTer4)
12g.76346081T>ACA385809103BBS10c.1904A>T (p.Asn635Ile)
12g.76346081T>CCA6694087BBS10c.1904A>G (p.Asn635Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.76346081T>GCA385809109BBS10c.1904A>C (p.Asn635Thr)
12g.76346081T=CA2047353152BBS10c.1904A= (p.Asn635=)
12g.76346082T>ACA385809113BBS10c.1903A>T (p.Asn635Tyr)
12g.76346082T>CCA385809119BBS10c.1903A>G (p.Asn635Asp)
dbSNP
12g.76346082T>GCA385809116BBS10c.1903A>C (p.Asn635His)
12g.76346082T=CA2047353153BBS10c.1903A= (p.Asn635=)
12g.76346083A>CCA481011168BBS10c.1902T>G (p.Ala634=)
12g.76346083A>GCA481011170BBS10c.1902T>C (p.Ala634=)
12g.76346083A>TCA481011171BBS10c.1902T>A (p.Ala634=)
12g.76346084G>ACA239331554BBS10c.1901C>T (p.Ala634Val)
dbSNP
12g.76346084G>CCA385809125BBS10c.1901C>G (p.Ala634Gly)
ClinVar dbSNP gnomAD v2 gnomAD v4
12g.76346084G=CA2047353154BBS10c.1901C= (p.Ala634=)
12g.76346084G>TCA385809123BBS10c.1901C>A (p.Ala634Asp)
12g.76346085C>ACA385809128BBS10c.1900G>T (p.Ala634Ser)
dbSNP
12g.76346085C=CA2047353155BBS10c.1900G= (p.Ala634=)
12g.76346085C>GCA385809130BBS10c.1900G>C (p.Ala634Pro)
12g.76346085C>TCA385809133BBS10c.1900G>A (p.Ala634Thr)
dbSNP
12g.76346086T>ACA481011181BBS10c.1899A>T (p.Ile633=)
ClinVar
12g.76346086T>CCA385809136BBS10c.1899A>G (p.Ile633Met)
gnomAD v4
12g.76346086T>GCA481011182BBS10c.1899A>C (p.Ile633=)
12g.76346087A>CCA385809141BBS10c.1898T>G (p.Ile633Arg)
12g.76346087A>GCA385809144BBS10c.1898T>C (p.Ile633Thr)
12g.76346087A>TCA385809147BBS10c.1898T>A (p.Ile633Lys)
12g.76346088T>ACA385809151BBS10c.1897A>T (p.Ile633Leu)
12g.76346088T>CCA385809152BBS10c.1897A>G (p.Ile633Val)
12g.76346088T>GCA385809153BBS10c.1897A>C (p.Ile633Leu)
12g.76346088_76346093delinsTTATCACA2047353156BBS10c.1892_1897delinsTGATAA (p.Met631=)
12g.76346089T>ACA481011191BBS10c.1896A>T (p.Ile632=)
12g.76346089T>CCA385809154BBS10c.1896A>G (p.Ile632Met)
ClinVar
12g.76346089T>GCA481011190BBS10c.1896A>C (p.Ile632=)
12g.76346091_76346095delCA691952349BBS10c.1892_1896del (p.Met631AsnfsTer3)
ClinVar dbSNP
12g.76346090A=CA2047353157BBS10c.1895T= (p.Ile632=)
12g.76346090A>CCA385809157BBS10c.1895T>G (p.Ile632Arg)
12g.76346090A>GCA239331557BBS10c.1895T>C (p.Ile632Thr)
dbSNP gnomAD v3 gnomAD v4
12g.76346090A>TCA385809156BBS10c.1895T>A (p.Ile632Lys)
12g.76346091T>ACA385809160BBS10c.1894A>T (p.Ile632Leu)
12g.76346091T>CCA385809167BBS10c.1894A>G (p.Ile632Val)
12g.76346091T>GCA385809171BBS10c.1894A>C (p.Ile632Leu)
12g.76346092C>ACA385809174BBS10c.1893G>T (p.Met631Ile)
dbSNP gnomAD v4
12g.76346092C=CA2047353158BBS10c.1893G= (p.Met631=)
12g.76346092C>GCA6694088BBS10c.1893G>C (p.Met631Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.76346092C>TCA385809179BBS10c.1893G>A (p.Met631Ile)
dbSNP
12g.76346092_76346096delCA2695217031BBS10c.1889_1893del (p.Ser630AsnfsTer4)
12g.76346093A=CA2047353159BBS10c.1892T= (p.Met631=)
12g.76346093A>CCA385809182BBS10c.1892T>G (p.Met631Arg)
12g.76346093A>GCA385809185BBS10c.1892T>C (p.Met631Thr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.76346093A>TCA385809187BBS10c.1892T>A (p.Met631Lys)
12g.76346094T>ACA385809189BBS10c.1891A>T (p.Met631Leu)
gnomAD v4
12g.76346094T>CCA385809192BBS10c.1891A>G (p.Met631Val)
ClinVar dbSNP gnomAD v4
12g.76346094T>GCA385809195BBS10c.1891A>C (p.Met631Leu)
12g.76346094T=CA2047353160BBS10c.1891A= (p.Met631=)
12g.76346094dupCA2619945588BBS10c.1891dup (p.Met631AsnfsTer5)
gnomAD v4
12g.76346095A>CCA385809202BBS10c.1890T>G (p.Ser630Arg)
12g.76346095A>GCA481011203BBS10c.1890T>C (p.Ser630=)
12g.76346095A>TCA385809199BBS10c.1890T>A (p.Ser630Arg)
12g.76346096C>ACA385809205BBS10c.1889G>T (p.Ser630Ile)
12g.76346096C=CA2047353161BBS10c.1889G= (p.Ser630=)
12g.76346096C>GCA385809209BBS10c.1889G>C (p.Ser630Thr)
gnomAD v4
12g.76346096C>TCA385809210BBS10c.1889G>A (p.Ser630Asn)
dbSNP gnomAD v2 gnomAD v4
12g.76346097T>ACA385809213BBS10c.1888A>T (p.Ser630Cys)
12g.76346097T>CCA385809216BBS10c.1888A>G (p.Ser630Gly)
gnomAD v4
12g.76346097T>GCA385809220BBS10c.1888A>C (p.Ser630Arg)
dbSNP gnomAD v2 gnomAD v4
12g.76346097T=CA2047353162BBS10c.1888A= (p.Ser630=)
12g.76346098A>CCA481010598BBS10c.1887T>G (p.Val629=)
12g.76346098A>GCA481010599BBS10c.1887T>C (p.Val629=)
12g.76346098A>TCA481010600BBS10c.1887T>A (p.Val629=)
gnomAD v4
12g.76346099A>CCA385809223BBS10c.1886T>G (p.Val629Gly)
12g.76346099A>GCA385809226BBS10c.1886T>C (p.Val629Ala)
12g.76346099A>TCA385809229BBS10c.1886T>A (p.Val629Asp)
12g.76346100C>ACA385809232BBS10c.1885G>T (p.Val629Phe)
12g.76346100C=CA2047353163BBS10c.1885G= (p.Val629=)
12g.76346100C>GCA6694089BBS10c.1885G>C (p.Val629Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.76346100C>TCA385809235BBS10c.1885G>A (p.Val629Ile)
12g.76346101C>ACA385809242BBS10c.1884G>T (p.Met628Ile)
12g.76346101C>GCA385809245BBS10c.1884G>C (p.Met628Ile)
12g.76346101C>TCA385809241BBS10c.1884G>A (p.Met628Ile)
12g.76346102A>CCA385809249BBS10c.1883T>G (p.Met628Arg)
12g.76346102A>GCA385809251BBS10c.1883T>C (p.Met628Thr)
gnomAD v4
12g.76346102A>TCA385809252BBS10c.1883T>A (p.Met628Lys)
12g.76346103T>ACA385809256BBS10c.1882A>T (p.Met628Leu)
12g.76346103T>CCA6694090BBS10c.1882A>G (p.Met628Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.76346103T>GCA385809266BBS10c.1882A>C (p.Met628Leu)
12g.76346103T=CA2047353164BBS10c.1882A= (p.Met628=)
12g.76346104G>ACA481010609BBS10c.1881C>T (p.Thr627=)
12g.76346104G>CCA481010613BBS10c.1881C>G (p.Thr627=)
dbSNP gnomAD v3 gnomAD v4
12g.76346104G=CA2047353165BBS10c.1881C= (p.Thr627=)
12g.76346104G>TCA481010622BBS10c.1881C>A (p.Thr627=)
12g.76346105G>ACA385809270BBS10c.1880C>T (p.Thr627Ile)
12g.76346105G>CCA385809275BBS10c.1880C>G (p.Thr627Ser)
12g.76346105G=CA2047353166BBS10c.1880C= (p.Thr627=)
12g.76346105G>TCA385809273BBS10c.1880C>A (p.Thr627Asn)
dbSNP gnomAD v2
12g.76346106T>ACA385809278BBS10c.1879A>T (p.Thr627Ser)
12g.76346106T>CCA385809281BBS10c.1879A>G (p.Thr627Ala)
12g.76346106T>GCA385809284BBS10c.1879A>C (p.Thr627Pro)
12g.76346107T>ACA385809287BBS10c.1878A>T (p.Glu626Asp)
12g.76346107T>CCA481010632BBS10c.1878A>G (p.Glu626=)
12g.76346107T>GCA385809290BBS10c.1878A>C (p.Glu626Asp)
12g.76346108T>ACA385809297BBS10c.1877A>T (p.Glu626Val)
12g.76346108T>CCA385809300BBS10c.1877A>G (p.Glu626Gly)
12g.76346108T>GCA385809294BBS10c.1877A>C (p.Glu626Ala)
12g.76346109C>ACA385809303BBS10c.1876G>T (p.Glu626Ter)
12g.76346109C>GCA385809307BBS10c.1876G>C (p.Glu626Gln)
12g.76346109C>TCA385809305BBS10c.1876G>A (p.Glu626Lys)
gnomAD v4
12g.76346110T>ACA385809311BBS10c.1875A>T (p.Glu625Asp)
gnomAD v4
12g.76346110T>CCA481010642BBS10c.1875A>G (p.Glu625=)
gnomAD v4
12g.76346110T>GCA385809314BBS10c.1875A>C (p.Glu625Asp)
12g.76346111T>ACA385809315BBS10c.1874A>T (p.Glu625Val)
12g.76346111T>CCA385809318BBS10c.1874A>G (p.Glu625Gly)
gnomAD v4
12g.76346111T>GCA385809327BBS10c.1874A>C (p.Glu625Ala)
12g.76346112C>ACA385809331BBS10c.1873G>T (p.Glu625Ter)
12g.76346112C>GCA385809333BBS10c.1873G>C (p.Glu625Gln)
12g.76346112C>TCA385809336BBS10c.1873G>A (p.Glu625Lys)
12g.76346113T>ACA481010647BBS10c.1872A>T (p.Ser624=)
12g.76346113T>CCA481010653BBS10c.1872A>G (p.Ser624=)
dbSNP gnomAD v3 gnomAD v4
12g.76346113T>GCA481010655BBS10c.1872A>C (p.Ser624=)
12g.76346113T=CA2047353167BBS10c.1872A= (p.Ser624=)
12g.76346114G>ACA385809339BBS10c.1871C>T (p.Ser624Leu)
ClinVar dbSNP
12g.76346114G>CCA6694091BBS10c.1871C>G (p.Ser624Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.76346114G=CA2047353168BBS10c.1871C= (p.Ser624=)
12g.76346114G>TCA385809343BBS10c.1871C>A (p.Ser624Ter)
12g.76346115A>CCA385809363BBS10c.1870T>G (p.Ser624Ala)
12g.76346115A>GCA385809366BBS10c.1870T>C (p.Ser624Pro)
12g.76346115A>TCA385809369BBS10c.1870T>A (p.Ser624Thr)
12g.76346116T>ACA385809375BBS10c.1869A>T (p.Gln623His)
12g.76346116T>CCA481010685BBS10c.1869A>G (p.Gln623=)
ClinVar gnomAD v4
12g.76346116T>GCA385809373BBS10c.1869A>C (p.Gln623His)
12g.76346117T>ACA385809381BBS10c.1868A>T (p.Gln623Leu)
12g.76346117T>CCA385809386BBS10c.1868A>G (p.Gln623Arg)
dbSNP
12g.76346117T>GCA385809391BBS10c.1868A>C (p.Gln623Pro)
12g.76346117T=CA2047353169BBS10c.1868A= (p.Gln623=)
12g.76346118G>ACA385809396BBS10c.1867C>T (p.Gln623Ter)
12g.76346118G>CCA385809399BBS10c.1867C>G (p.Gln623Glu)
12g.76346118G>TCA385809402BBS10c.1867C>A (p.Gln623Lys)
gnomAD v4
12g.76346119A=CA2047353170BBS10c.1866T= (p.His622=)
12g.76346119A>CCA385809406BBS10c.1866T>G (p.His622Gln)
12g.76346119A>GCA481010699BBS10c.1866T>C (p.His622=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.76346119A>TCA385809409BBS10c.1866T>A (p.His622Gln)
12g.76346119_76346129delinsATGGCATTTTTCA2047353171BBS10c.1856_1866delinsAAAAATGCCAT (p.Lys619=)
12g.76346120T>ACA385809419BBS10c.1865A>T (p.His622Leu)
12g.76346120T>CCA385809421BBS10c.1865A>G (p.His622Arg)
ClinVar dbSNP gnomAD v4
12g.76346120T>GCA385809423BBS10c.1865A>C (p.His622Pro)
12g.76346120T=CA2047353172BBS10c.1865A= (p.His622=)
12g.76346126_76346135delCA356963BBS10c.1856_1865del (p.Lys619IlefsTer10)
ClinVar dbSNP
12g.76346121G>ACA6694092BBS10c.1864C>T (p.His622Tyr)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.76346121G>CCA385809435BBS10c.1864C>G (p.His622Asp)
12g.76346121G=CA2047353173BBS10c.1864C= (p.His622=)
12g.76346121G>TCA385809432BBS10c.1864C>A (p.His622Asn)
dbSNP
12g.76346122G>ACA481010706BBS10c.1863C>T (p.Cys621=)
dbSNP
12g.76346122G>CCA385809441BBS10c.1863C>G (p.Cys621Trp)
12g.76346122G=CA2047353174BBS10c.1863C= (p.Cys621=)
12g.76346122G>TCA385809443BBS10c.1863C>A (p.Cys621Ter)
12g.76346123C>ACA385809447BBS10c.1862G>T (p.Cys621Phe)
12g.76346123C>GCA385809450BBS10c.1862G>C (p.Cys621Ser)
12g.76346123C>TCA385809453BBS10c.1862G>A (p.Cys621Tyr)
12g.76346124A>CCA385809456BBS10c.1861T>G (p.Cys621Gly)
12g.76346124A>GCA385809457BBS10c.1861T>C (p.Cys621Arg)
12g.76346124A>TCA385809461BBS10c.1861T>A (p.Cys621Ser)
12g.76346125T>ACA385809464BBS10c.1860A>T (p.Lys620Asn)
12g.76346125T>CCA481010725BBS10c.1860A>G (p.Lys620=)
12g.76346125T>GCA6694093BBS10c.1860A>C (p.Lys620Asn)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.76346125T=CA2047353175BBS10c.1860A= (p.Lys620=)
12g.76346130dupCA2695199108BBS10c.1860dup (p.Cys621MetfsTer10)
ClinVar
12g.76346130delCA481010722BBS10c.1860del (p.Lys620AsnfsTer12)
gnomAD v4 COSMIC
12g.76346126T>ACA385809469BBS10c.1859A>T (p.Lys620Ile)
COSMIC
12g.76346126T>CCA385809472BBS10c.1859A>G (p.Lys620Arg)
12g.76346126T>GCA6694094BBS10c.1859A>C (p.Lys620Thr)
dbSNP ExAC gnomAD v2
12g.76346126T=CA2047353176BBS10c.1859A= (p.Lys620=)
12g.76346127T>ACA385809478BBS10c.1858A>T (p.Lys620Ter)
12g.76346127T>CCA385809484BBS10c.1858A>G (p.Lys620Glu)
12g.76346127T>GCA385809481BBS10c.1858A>C (p.Lys620Gln)
12g.76346128T>ACA385809486BBS10c.1857A>T (p.Lys619Asn)
12g.76346128T>CCA481010727BBS10c.1857A>G (p.Lys619=)
12g.76346128T>GCA385809489BBS10c.1857A>C (p.Lys619Asn)
gnomAD v4
12g.76346129T>ACA385809501BBS10c.1856A>T (p.Lys619Ile)
12g.76346129T>CCA385809504BBS10c.1856A>G (p.Lys619Arg)
ClinVar dbSNP gnomAD v4
12g.76346129T>GCA385809506BBS10c.1856A>C (p.Lys619Thr)
12g.76346129T=CA2047353177BBS10c.1856A= (p.Lys619=)
12g.76346130T>ACA385809510BBS10c.1855A>T (p.Lys619Ter)
12g.76346130T>CCA385809513BBS10c.1855A>G (p.Lys619Glu)
12g.76346130T>GCA385809516BBS10c.1855A>C (p.Lys619Gln)
12g.76346131G>ACA481010739BBS10c.1854C>T (p.Ala618=)
ClinVar dbSNP gnomAD v4
12g.76346131G>CCA481010741BBS10c.1854C>G (p.Ala618=)
12g.76346131G>TCA481010744BBS10c.1854C>A (p.Ala618=)
12g.76346132G>ACA385809519BBS10c.1853C>T (p.Ala618Val)
12g.76346132G>CCA385809522BBS10c.1853C>G (p.Ala618Gly)
12g.76346132G>TCA385809525BBS10c.1853C>A (p.Ala618Asp)
12g.76346133C>ACA385809534BBS10c.1852G>T (p.Ala618Ser)
12g.76346133C>GCA385809531BBS10c.1852G>C (p.Ala618Pro)
12g.76346133C>TCA385809529BBS10c.1852G>A (p.Ala618Thr)
12g.76346134A>CCA385809540BBS10c.1851T>G (p.Tyr617Ter)
12g.76346134A>GCA481010749BBS10c.1851T>C (p.Tyr617=)
ClinVar gnomAD v4
12g.76346134A>TCA385809537BBS10c.1851T>A (p.Tyr617Ter)
12g.76346135T>ACA385809549BBS10c.1850A>T (p.Tyr617Phe)
12g.76346135T>CCA6694095BBS10c.1850A>G (p.Tyr617Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.76346135T>GCA385809547BBS10c.1850A>C (p.Tyr617Ser)
12g.76346135T=CA2047353178BBS10c.1850A= (p.Tyr617=)
12g.76346136A>CCA385809552BBS10c.1849T>G (p.Tyr617Asp)
12g.76346136A>GCA385809555BBS10c.1849T>C (p.Tyr617His)
12g.76346136A>TCA385809558BBS10c.1849T>A (p.Tyr617Asn)
12g.76346137A=CA2047353179BBS10c.1848T= (p.Asn616=)
12g.76346137A>CCA385809561BBS10c.1848T>G (p.Asn616Lys)
dbSNP gnomAD v2 gnomAD v4
12g.76346137A>GCA481010757BBS10c.1848T>C (p.Asn616=)
gnomAD v4
12g.76346137A>TCA385809563BBS10c.1848T>A (p.Asn616Lys)
12g.76346138T>ACA385809566BBS10c.1847A>T (p.Asn616Ile)
12g.76346138T>CCA6694096BBS10c.1847A>G (p.Asn616Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.76346138T>GCA385809570BBS10c.1847A>C (p.Asn616Thr)
12g.76346138T=CA2047353180BBS10c.1847A= (p.Asn616=)
12g.76346139T>ACA385809575BBS10c.1846A>T (p.Asn616Tyr)
12g.76346139T>CCA385809578BBS10c.1846A>G (p.Asn616Asp)
12g.76346139T>GCA6694097BBS10c.1846A>C (p.Asn616His)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.76346139T=CA2047353181BBS10c.1846A= (p.Asn616=)
12g.76346140G>ACA481010766BBS10c.1845C>T (p.Leu615=)
12g.76346140G>CCA481010767BBS10c.1845C>G (p.Leu615=)
12g.76346140G>TCA481010764BBS10c.1845C>A (p.Leu615=)
gnomAD v4
12g.76346140_76346142delCA2619945589BBS10c.1843_1845del (p.Leu615del)
gnomAD v4
12g.76346141A>CCA385809588BBS10c.1844T>G (p.Leu615Arg)
12g.76346141A>GCA385809582BBS10c.1844T>C (p.Leu615Pro)
12g.76346141A>TCA385809585BBS10c.1844T>A (p.Leu615His)
12g.76346142G>ACA385809591BBS10c.1843C>T (p.Leu615Phe)
12g.76346142G>CCA385809592BBS10c.1843C>G (p.Leu615Val)
12g.76346142G>TCA385809594BBS10c.1843C>A (p.Leu615Ile)
12g.76346143A>CCA481010776BBS10c.1842T>G (p.Leu614=)
12g.76346143A>GCA481010774BBS10c.1842T>C (p.Leu614=)
12g.76346143A>TCA481010775BBS10c.1842T>A (p.Leu614=)
12g.76346144A>CCA385809598BBS10c.1841T>G (p.Leu614Arg)
12g.76346144A>GCA385809601BBS10c.1841T>C (p.Leu614Pro)
12g.76346144A>TCA385809604BBS10c.1841T>A (p.Leu614His)
12g.76346145G>ACA385809607BBS10c.1840C>T (p.Leu614Phe)
12g.76346145G>CCA385809618BBS10c.1840C>G (p.Leu614Val)
12g.76346145G>TCA385809621BBS10c.1840C>A (p.Leu614Ile)
12g.76346146A=CA2047353182BBS10c.1839T= (p.Tyr613=)
12g.76346146A>CCA385809625BBS10c.1839T>G (p.Tyr613Ter)
12g.76346146A>GCA481010791BBS10c.1839T>C (p.Tyr613=)
12g.76346146A>TCA385809627BBS10c.1839T>A (p.Tyr613Ter)
ClinVar dbSNP
12g.76346147T>ACA385809633BBS10c.1838A>T (p.Tyr613Phe)
12g.76346147T>CCA241802BBS10c.1838A>G (p.Tyr613Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.76346147T>GCA385809630BBS10c.1838A>C (p.Tyr613Ser)
12g.76346147T=CA2047353183BBS10c.1838A= (p.Tyr613=)
12g.76346148A=CA2047353184BBS10c.1837T= (p.Tyr613=)
12g.76346148A>CCA385809638BBS10c.1837T>G (p.Tyr613Asp)
gnomAD v4
12g.76346148A>GCA6694098BBS10c.1837T>C (p.Tyr613His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.76346148A>TCA385809643BBS10c.1837T>A (p.Tyr613Asn)
12g.76346149G>ACA481010797BBS10c.1836C>T (p.Tyr612=)
12g.76346149G>CCA385809646BBS10c.1836C>G (p.Tyr612Ter)
12g.76346149G>TCA385809649BBS10c.1836C>A (p.Tyr612Ter)
12g.76346150T>ACA385809653BBS10c.1835A>T (p.Tyr612Phe)
12g.76346150T>CCA385809655BBS10c.1835A>G (p.Tyr612Cys)
gnomAD v4
12g.76346150T>GCA385809659BBS10c.1835A>C (p.Tyr612Ser)
12g.76346151A>CCA385809666BBS10c.1834T>G (p.Tyr612Asp)
12g.76346151A>GCA385809671BBS10c.1834T>C (p.Tyr612His)
12g.76346151A>TCA385809675BBS10c.1834T>A (p.Tyr612Asn)
12g.76346152delCA2573148986BBS10c.1834del (p.Tyr612ThrfsTer20)
ClinVar dbSNP
12g.76346152A>CCA385809678BBS10c.1833T>G (p.His611Gln)
12g.76346152A>GCA481010816BBS10c.1833T>C (p.His611=)
12g.76346152A>TCA385809681BBS10c.1833T>A (p.His611Gln)
12g.76346153T>ACA385809691BBS10c.1832A>T (p.His611Leu)
12g.76346153T>CCA385809685BBS10c.1832A>G (p.His611Arg)
dbSNP
12g.76346153T>GCA385809688BBS10c.1832A>C (p.His611Pro)
12g.76346153T=CA2047353185BBS10c.1832A= (p.His611=)
12g.76346154G>ACA385809694BBS10c.1831C>T (p.His611Tyr)
12g.76346154G>CCA385809696BBS10c.1831C>G (p.His611Asp)
gnomAD v4
12g.76346154G>TCA385809698BBS10c.1831C>A (p.His611Asn)
12g.76346155T>ACA385809703BBS10c.1830A>T (p.Leu610Phe)
12g.76346155T>CCA481010825BBS10c.1830A>G (p.Leu610=)
12g.76346155T>GCA385809706BBS10c.1830A>C (p.Leu610Phe)
12g.76346155_76346156insTTCA2619945590BBS10c.1830_1831insAA (p.His611AsnfsTer22)
gnomAD v4
12g.76346156A=CA2047353186BBS10c.1829T= (p.Leu610=)
12g.76346156A>CCA385809712BBS10c.1829T>G (p.Leu610Ter)
ClinVar dbSNP gnomAD v4
12g.76346156A>GCA385809715BBS10c.1829T>C (p.Leu610Ser)
12g.76346156A>TCA385809718BBS10c.1829T>A (p.Leu610Ter)
12g.76346157A>CCA385809721BBS10c.1828T>G (p.Leu610Val)
gnomAD v4
12g.76346157A>GCA481010834BBS10c.1828T>C (p.Leu610=)
ClinVar
12g.76346157A>TCA385809724BBS10c.1828T>A (p.Leu610Ile)
12g.76346158C>ACA6694099BBS10c.1827G>T (p.Leu609Phe)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.76346158C=CA2047353187BBS10c.1827G= (p.Leu609=)
12g.76346158C>GCA385809730BBS10c.1827G>C (p.Leu609Phe)
12g.76346158C>TCA481010837BBS10c.1827G>A (p.Leu609=)
ClinVar dbSNP gnomAD v4
12g.76346159A=CA2047353188BBS10c.1826T= (p.Leu609=)
12g.76346159A>CCA385809737BBS10c.1826T>G (p.Leu609Trp)
dbSNP gnomAD v3 gnomAD v4
12g.76346159A>GCA385809740BBS10c.1826T>C (p.Leu609Ser)
ClinVar gnomAD v4
12g.76346159A>TCA385809735BBS10c.1826T>A (p.Leu609Ter)
12g.76346160A>CCA385809743BBS10c.1825T>G (p.Leu609Val)
12g.76346160A>GCA481010845BBS10c.1825T>C (p.Leu609=)
ClinVar dbSNP gnomAD v4
12g.76346160A>TCA385809746BBS10c.1825T>A (p.Leu609Met)
12g.76346161G>ACA6694100BBS10c.1824C>T (p.Ile608=)
ClinVar dbSNP ExAC gnomAD v2
12g.76346161G>CCA385809750BBS10c.1824C>G (p.Ile608Met)
12g.76346161G=CA2047353189BBS10c.1824C= (p.Ile608=)
12g.76346161G>TCA481010849BBS10c.1824C>A (p.Ile608=)
gnomAD v4
12g.76346162A>CCA385809754BBS10c.1823T>G (p.Ile608Ser)
12g.76346162A>GCA385809756BBS10c.1823T>C (p.Ile608Thr)
12g.76346162A>TCA385809759BBS10c.1823T>A (p.Ile608Asn)
gnomAD v4
12g.76346163T>ACA385809762BBS10c.1822A>T (p.Ile608Phe)
12g.76346163T>CCA16606610BBS10c.1822A>G (p.Ile608Val)
ClinVar dbSNP gnomAD v4
12g.76346163T>GCA385809767BBS10c.1822A>C (p.Ile608Leu)
12g.76346163T=CA2047353190BBS10c.1822A= (p.Ile608=)
12g.76346164C>ACA239331605BBS10c.1821G>T (p.Glu607Asp)
dbSNP
12g.76346164C=CA2047353191BBS10c.1821G= (p.Glu607=)
12g.76346164C>GCA385809773BBS10c.1821G>C (p.Glu607Asp)
12g.76346164C>TCA481010860BBS10c.1821G>A (p.Glu607=)
12g.76346165T>ACA385809776BBS10c.1820A>T (p.Glu607Val)
12g.76346165T>CCA385809778BBS10c.1820A>G (p.Glu607Gly)
12g.76346165T>GCA385809782BBS10c.1820A>C (p.Glu607Ala)
12g.76346166C>ACA385809795BBS10c.1819G>T (p.Glu607Ter)
12g.76346166C>GCA385809790BBS10c.1819G>C (p.Glu607Gln)
12g.76346166C>TCA385809787BBS10c.1819G>A (p.Glu607Lys)
12g.76346167A>CCA385809799BBS10c.1818T>G (p.Phe606Leu)
12g.76346167A>GCA481010868BBS10c.1818T>C (p.Phe606=)
12g.76346167A>TCA385809802BBS10c.1818T>A (p.Phe606Leu)
12g.76346168A>CCA385809806BBS10c.1817T>G (p.Phe606Cys)
12g.76346168A>GCA385809808BBS10c.1817T>C (p.Phe606Ser)
12g.76346168A>TCA385809812BBS10c.1817T>A (p.Phe606Tyr)
12g.76346169A>CCA385809817BBS10c.1816T>G (p.Phe606Val)
12g.76346169A>GCA385809819BBS10c.1816T>C (p.Phe606Leu)
12g.76346169A>TCA385809826BBS10c.1816T>A (p.Phe606Ile)
12g.76346170A>CCA385809828BBS10c.1815T>G (p.Asn605Lys)
12g.76346170A>GCA481010875BBS10c.1815T>C (p.Asn605=)
gnomAD v4
12g.76346170A>TCA385809831BBS10c.1815T>A (p.Asn605Lys)
12g.76346170_76346171delCA2573148987BBS10c.1814_1815del (p.Asn605IlefsTer2)
ClinVar dbSNP
12g.76346171T>ACA385809832BBS10c.1814A>T (p.Asn605Ile)
12g.76346171T>CCA385809833BBS10c.1814A>G (p.Asn605Ser)
12g.76346171T>GCA385809834BBS10c.1814A>C (p.Asn605Thr)
12g.76346172T>ACA385809837BBS10c.1813A>T (p.Asn605Tyr)
12g.76346172T>CCA385809840BBS10c.1813A>G (p.Asn605Asp)
12g.76346172T>GCA385809836BBS10c.1813A>C (p.Asn605His)
12g.76346173A=CA2047353192BBS10c.1812T= (p.Gly604=)
12g.76346173A>CCA481010884BBS10c.1812T>G (p.Gly604=)
12g.76346173A>GCA239331608BBS10c.1812T>C (p.Gly604=)
ClinVar dbSNP gnomAD v2 gnomAD v4
12g.76346173A>TCA481010885BBS10c.1812T>A (p.Gly604=)
12g.76346173dupCA2739272194BBS10c.1812dup (p.Asn605Ter)
ClinVar
12g.76346174C>ACA385809843BBS10c.1811G>T (p.Gly604Val)
12g.76346174C=CA2047353193BBS10c.1811G= (p.Gly604=)
12g.76346174C>GCA385809844BBS10c.1811G>C (p.Gly604Ala)
ClinVar dbSNP
12g.76346174C>TCA385809846BBS10c.1811G>A (p.Gly604Asp)
12g.76346175C>ACA385809848BBS10c.1810G>T (p.Gly604Cys)
12g.76346175C>GCA385809849BBS10c.1810G>C (p.Gly604Arg)
12g.76346175C>TCA385809851BBS10c.1810G>A (p.Gly604Ser)
12g.76346176A>CCA481010893BBS10c.1809T>G (p.Gly603=)
12g.76346176A>GCA481010895BBS10c.1809T>C (p.Gly603=)
ClinVar dbSNP gnomAD v4
12g.76346176A>TCA481010896BBS10c.1809T>A (p.Gly603=)
12g.76346177C>ACA385809853BBS10c.1808G>T (p.Gly603Val)
12g.76346177C>GCA385809854BBS10c.1808G>C (p.Gly603Ala)
12g.76346177C>TCA385809857BBS10c.1808G>A (p.Gly603Asp)
12g.76346178C>ACA6694101BBS10c.1807G>T (p.Gly603Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.76346178C=CA2047353194BBS10c.1807G= (p.Gly603=)
12g.76346178C>GCA385809861BBS10c.1807G>C (p.Gly603Arg)
dbSNP
12g.76346178C>TCA385809862BBS10c.1807G>A (p.Gly603Ser)
ClinVar dbSNP gnomAD v3 gnomAD v4
12g.76346179T>ACA481010910BBS10c.1806A>T (p.Val602=)
12g.76346179T>CCA481010912BBS10c.1806A>G (p.Val602=)
ClinVar dbSNP gnomAD v4
12g.76346179T>GCA481010913BBS10c.1806A>C (p.Val602=)
12g.76346179T=CA2047353195BBS10c.1806A= (p.Val602=)
12g.76346180A>CCA385809866BBS10c.1805T>G (p.Val602Gly)
12g.76346180A>GCA385809863BBS10c.1805T>C (p.Val602Ala)
12g.76346180A>TCA385809864BBS10c.1805T>A (p.Val602Glu)
12g.76346181C>ACA385809868BBS10c.1804G>T (p.Val602Leu)
ClinVar dbSNP
12g.76346181C=CA2047353196BBS10c.1804G= (p.Val602=)
12g.76346181C>GCA6694102BBS10c.1804G>C (p.Val602Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.76346181C>TCA385809870BBS10c.1804G>A (p.Val602Ile)
gnomAD v4
12g.76346181dupCA2796591353BBS10c.1804dup (p.Val602GlyfsTer4)

Number of alleles fetched