Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.110812431C>ACA378371047RBM20c.2034C>A (p.His678Gln)
c.1650C>A (p.His550Gln)
c.1869C>A (p.His623Gln)
 dbSNP
10g.110812431C>GCA378371048RBM20c.2034C>G (p.His678Gln)
c.1650C>G (p.His550Gln)
c.1869C>G (p.His623Gln)
 dbSNP
10g.110812431C>TCA471368129RBM20c.2034C>T (p.His678=)
c.1650C>T (p.His550=)
c.1869C>T (p.His623=)
10g.110812432T>ACA378371050RBM20c.2035T>A (p.Ser679Thr)
c.1651T>A (p.Ser551Thr)
c.1870T>A (p.Ser624Thr)
10g.110812432T>CCA378371053RBM20c.2035T>C (p.Ser679Pro)
c.1651T>C (p.Ser551Pro)
c.1870T>C (p.Ser624Pro)
10g.110812432T>GCA378371052RBM20c.2035T>G (p.Ser679Ala)
c.1651T>G (p.Ser551Ala)
c.1870T>G (p.Ser624Ala)
10g.110812433C>ACA378371056RBM20c.2036C>A (p.Ser679Tyr)
c.1652C>A (p.Ser551Tyr)
c.1871C>A (p.Ser624Tyr)
10g.110812433C>GCA378371061RBM20c.2036C>G (p.Ser679Cys)
c.1652C>G (p.Ser551Cys)
c.1871C>G (p.Ser624Cys)
10g.110812433C>TCA378371063RBM20c.2036C>T (p.Ser679Phe)
c.1652C>T (p.Ser551Phe)
c.1871C>T (p.Ser624Phe)
 dbSNP gnomAD v3 gnomAD v4
10g.110812434T>ACA471368131RBM20c.2037T>A (p.Ser679=)
c.1653T>A (p.Ser551=)
c.1872T>A (p.Ser624=)
10g.110812434T>CCA471368133RBM20c.2037T>C (p.Ser679=)
c.1653T>C (p.Ser551=)
c.1872T>C (p.Ser624=)
10g.110812434T>GCA471368132RBM20c.2037T>G (p.Ser679=)
c.1653T>G (p.Ser551=)
c.1872T>G (p.Ser624=)
10g.110812435C>ACA378371066RBM20c.2038C>A (p.Pro680Thr)
c.1654C>A (p.Pro552Thr)
c.1873C>A (p.Pro625Thr)
10g.110812435C>GCA378371068RBM20c.2038C>G (p.Pro680Ala)
c.1654C>G (p.Pro552Ala)
c.1873C>G (p.Pro625Ala)
10g.110812435C>TCA378371071RBM20c.2038C>T (p.Pro680Ser)
c.1654C>T (p.Pro552Ser)
c.1873C>T (p.Pro625Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v4
10g.110812436C>ACA378371073RBM20c.2039C>A (p.Pro680His)
c.1655C>A (p.Pro552His)
c.1874C>A (p.Pro625His)
10g.110812436C>GCA378371076RBM20c.2039C>G (p.Pro680Arg)
c.1655C>G (p.Pro552Arg)
c.1874C>G (p.Pro625Arg)
10g.110812436C>TCA378371079RBM20c.2039C>T (p.Pro680Leu)
c.1655C>T (p.Pro552Leu)
c.1874C>T (p.Pro625Leu)
10g.110812437C>ACA471368134RBM20c.2040C>A (p.Pro680=)
c.1656C>A (p.Pro552=)
c.1875C>A (p.Pro625=)
10g.110812437C>GCA471368135RBM20c.2040C>G (p.Pro680=)
c.1656C>G (p.Pro552=)
c.1875C>G (p.Pro625=)
10g.110812437C>TCA213223715RBM20c.2040C>T (p.Pro680=)
c.1656C>T (p.Pro552=)
c.1875C>T (p.Pro625=)
 dbSNP
10g.110812438T>ACA378371091RBM20c.2041T>A (p.Tyr681Asn)
c.1657T>A (p.Tyr553Asn)
c.1876T>A (p.Tyr626Asn)
10g.110812438T>CCA378371090RBM20c.2041T>C (p.Tyr681His)
c.1657T>C (p.Tyr553His)
c.1876T>C (p.Tyr626His)
 ClinVar dbSNP gnomAD v4
10g.110812438T>GCA378371088RBM20c.2041T>G (p.Tyr681Asp)
c.1657T>G (p.Tyr553Asp)
c.1876T>G (p.Tyr626Asp)
10g.110812439delCA2739276021RBM20c.2042del (p.Tyr681LeufsTer?)
c.1658del (p.Tyr553LeufsTer?)
c.1877del (p.Tyr626LeufsTer?)
 ClinVar
10g.110812439A>CCA378371093RBM20c.2042A>C (p.Tyr681Ser)
c.1658A>C (p.Tyr553Ser)
c.1877A>C (p.Tyr626Ser)
10g.110812439A>GCA5688663RBM20c.2042A>G (p.Tyr681Cys)
c.1658A>G (p.Tyr553Cys)
c.1877A>G (p.Tyr626Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.110812439A>TCA378371096RBM20c.2042A>T (p.Tyr681Phe)
c.1658A>T (p.Tyr553Phe)
c.1877A>T (p.Tyr626Phe)
10g.110812440T>ACA378371110RBM20c.2043T>A (p.Tyr681Ter)
c.1659T>A (p.Tyr553Ter)
c.1878T>A (p.Tyr626Ter)
 ClinVar dbSNP
10g.110812440T>CCA5688664RBM20c.2043T>C (p.Tyr681=)
c.1659T>C (p.Tyr553=)
c.1878T>C (p.Tyr626=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.110812440T>GCA378371112RBM20c.2043T>G (p.Tyr681Ter)
c.1659T>G (p.Tyr553Ter)
c.1878T>G (p.Tyr626Ter)
10g.110812441G>ACA378371113RBM20c.2044G>A (p.Ala682Thr)
c.1660G>A (p.Ala554Thr)
c.1879G>A (p.Ala627Thr)
 gnomAD v4
10g.110812441G>CCA378371114RBM20c.2044G>C (p.Ala682Pro)
c.1660G>C (p.Ala554Pro)
c.1879G>C (p.Ala627Pro)
 dbSNP
10g.110812441G>TCA378371116RBM20c.2044G>T (p.Ala682Ser)
c.1660G>T (p.Ala554Ser)
c.1879G>T (p.Ala627Ser)
10g.110812442C>ACA378371119RBM20c.2045C>A (p.Ala682Asp)
c.1661C>A (p.Ala554Asp)
c.1880C>A (p.Ala627Asp)
10g.110812442C>GCA378371121RBM20c.2045C>G (p.Ala682Gly)
c.1661C>G (p.Ala554Gly)
c.1880C>G (p.Ala627Gly)
 ClinVar dbSNP gnomAD v3 gnomAD v4
10g.110812442C>TCA378371127RBM20c.2045C>T (p.Ala682Val)
c.1661C>T (p.Ala554Val)
c.1880C>T (p.Ala627Val)
 dbSNP gnomAD v3 gnomAD v4
10g.110812443C>ACA471506815RBM20c.2046C>A (p.Ala682=)
c.1662C>A (p.Ala554=)
c.1881C>A (p.Ala627=)
10g.110812443C>GCA471506817RBM20c.2046C>G (p.Ala682=)
c.1662C>G (p.Ala554=)
c.1881C>G (p.Ala627=)
 gnomAD v4
10g.110812443C>TCA213223726RBM20c.2046C>T (p.Ala682=)
c.1662C>T (p.Ala554=)
c.1881C>T (p.Ala627=)
 ClinVar dbSNP gnomAD v4
10g.110812444A>CCA471506818RBM20c.2047A>C (p.Arg683=)
c.1663A>C (p.Arg555=)
c.1882A>C (p.Arg628=)
10g.110812444A>GCA378371132RBM20c.2047A>G (p.Arg683Gly)
c.1663A>G (p.Arg555Gly)
c.1882A>G (p.Arg628Gly)
 ClinVar dbSNP gnomAD v4
10g.110812444A>TCA378371139RBM20c.2047A>T (p.Arg683Trp)
c.1663A>T (p.Arg555Trp)
c.1882A>T (p.Arg628Trp)
10g.110812445G>ACA378371142RBM20c.2048G>A (p.Arg683Lys)
c.1664G>A (p.Arg555Lys)
c.1883G>A (p.Arg628Lys)
 gnomAD v4
10g.110812445G>CCA378371150RBM20c.2048G>C (p.Arg683Thr)
c.1664G>C (p.Arg555Thr)
c.1883G>C (p.Arg628Thr)
10g.110812445G>TCA378371152RBM20c.2048G>T (p.Arg683Met)
c.1664G>T (p.Arg555Met)
c.1883G>T (p.Arg628Met)
10g.110812450_110812453delCA2697558788RBM20c.2053_2056del (p.Glu685LysfsTer?)
c.1669_1672del (p.Glu557LysfsTer?)
c.1888_1891del (p.Glu630LysfsTer?)
 ClinVar
10g.110812446G>ACA471506821RBM20c.2049G>A (p.Arg683=)
c.1665G>A (p.Arg555=)
c.1884G>A (p.Arg628=)
10g.110812446G>CCA378371156RBM20c.2049G>C (p.Arg683Ser)
c.1665G>C (p.Arg555Ser)
c.1884G>C (p.Arg628Ser)
 dbSNP gnomAD v3 gnomAD v4
10g.110812446G>TCA378371158RBM20c.2049G>T (p.Arg683Ser)
c.1665G>T (p.Arg555Ser)
c.1884G>T (p.Arg628Ser)
10g.110812447A>CCA471506823RBM20c.2050A>C (p.Arg684=)
c.1666A>C (p.Arg556=)
c.1885A>C (p.Arg629=)
10g.110812447A>GCA378371159RBM20c.2050A>G (p.Arg684Gly)
c.1666A>G (p.Arg556Gly)
c.1885A>G (p.Arg629Gly)
10g.110812447A>TCA378371162RBM20c.2050A>T (p.Arg684Trp)
c.1666A>T (p.Arg556Trp)
c.1885A>T (p.Arg629Trp)
10g.110812448G>ACA213223735RBM20c.2051G>A (p.Arg684Lys)
c.1667G>A (p.Arg556Lys)
c.1886G>A (p.Arg629Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.110812448G>CCA378371163RBM20c.2051G>C (p.Arg684Thr)
c.1667G>C (p.Arg556Thr)
c.1886G>C (p.Arg629Thr)
10g.110812448G>TCA378371165RBM20c.2051G>T (p.Arg684Met)
c.1667G>T (p.Arg556Met)
c.1886G>T (p.Arg629Met)
 ClinVar
10g.110812449G>ACA471506828RBM20c.2052G>A (p.Arg684=)
c.1668G>A (p.Arg556=)
c.1887G>A (p.Arg629=)
10g.110812449G>CCA378371166RBM20c.2052G>C (p.Arg684Ser)
c.1668G>C (p.Arg556Ser)
c.1887G>C (p.Arg629Ser)
 COSMIC
10g.110812449G>TCA378371168RBM20c.2052G>T (p.Arg684Ser)
c.1668G>T (p.Arg556Ser)
c.1887G>T (p.Arg629Ser)
10g.110812450G>ACA378371171RBM20c.2053G>A (p.Glu685Lys)
c.1669G>A (p.Glu557Lys)
c.1888G>A (p.Glu630Lys)
10g.110812450G>CCA378371178RBM20c.2053G>C (p.Glu685Gln)
c.1669G>C (p.Glu557Gln)
c.1888G>C (p.Glu630Gln)
10g.110812450G>TCA378371187RBM20c.2053G>T (p.Glu685Ter)
c.1669G>T (p.Glu557Ter)
c.1888G>T (p.Glu630Ter)
10g.110812451A>CCA378371189RBM20c.2054A>C (p.Glu685Ala)
c.1670A>C (p.Glu557Ala)
c.1889A>C (p.Glu630Ala)
 gnomAD v4
10g.110812451A>GCA378371190RBM20c.2054A>G (p.Glu685Gly)
c.1670A>G (p.Glu557Gly)
c.1889A>G (p.Glu630Gly)
10g.110812451A>TCA378371188RBM20c.2054A>T (p.Glu685Val)
c.1670A>T (p.Glu557Val)
c.1889A>T (p.Glu630Val)
10g.110812452G>ACA471506829RBM20c.2055G>A (p.Glu685=)
c.1671G>A (p.Glu557=)
c.1890G>A (p.Glu630=)
 gnomAD v4
10g.110812452G>CCA378371195RBM20c.2055G>C (p.Glu685Asp)
c.1671G>C (p.Glu557Asp)
c.1890G>C (p.Glu630Asp)
10g.110812452G>TCA378371198RBM20c.2055G>T (p.Glu685Asp)
c.1671G>T (p.Glu557Asp)
c.1890G>T (p.Glu630Asp)
10g.110812453G>ACA378371199RBM20c.2056G>A (p.Glu686Lys)
c.1672G>A (p.Glu558Lys)
c.1891G>A (p.Glu631Lys)
 gnomAD v4
10g.110812453G>CCA378371201RBM20c.2056G>C (p.Glu686Gln)
c.1672G>C (p.Glu558Gln)
c.1891G>C (p.Glu631Gln)
10g.110812453G>TCA378371204RBM20c.2056G>T (p.Glu686Ter)
c.1672G>T (p.Glu558Ter)
c.1891G>T (p.Glu631Ter)
10g.110812454A>CCA378371205RBM20c.2057A>C (p.Glu686Ala)
c.1673A>C (p.Glu558Ala)
c.1892A>C (p.Glu631Ala)
10g.110812454A>GCA378371206RBM20c.2057A>G (p.Glu686Gly)
c.1673A>G (p.Glu558Gly)
c.1892A>G (p.Glu631Gly)
10g.110812454A>TCA378371207RBM20c.2057A>T (p.Glu686Val)
c.1673A>T (p.Glu558Val)
c.1892A>T (p.Glu631Val)
10g.110812455A>CCA378371208RBM20c.2058A>C (p.Glu686Asp)
c.1674A>C (p.Glu558Asp)
c.1893A>C (p.Glu631Asp)
10g.110812455A>GCA471506835RBM20c.2058A>G (p.Glu686=)
c.1674A>G (p.Glu558=)
c.1893A>G (p.Glu631=)
 dbSNP gnomAD v4
10g.110812455A>TCA378371209RBM20c.2058A>T (p.Glu686Asp)
c.1674A>T (p.Glu558Asp)
c.1893A>T (p.Glu631Asp)
10g.110812456G>ACA378371216RBM20c.2059G>A (p.Glu687Lys)
c.1675G>A (p.Glu559Lys)
c.1894G>A (p.Glu632Lys)
10g.110812456G>CCA378371219RBM20c.2059G>C (p.Glu687Gln)
c.1675G>C (p.Glu559Gln)
c.1894G>C (p.Glu632Gln)
10g.110812456G>TCA378371225RBM20c.2059G>T (p.Glu687Ter)
c.1675G>T (p.Glu559Ter)
c.1894G>T (p.Glu632Ter)
10g.110812457delCA2697558789RBM20c.2060del (p.Glu687GlyfsTer?)
c.1676del (p.Glu559GlyfsTer?)
c.1895del (p.Glu632GlyfsTer?)
 ClinVar
10g.110812457A>CCA378371233RBM20c.2060A>C (p.Glu687Ala)
c.1676A>C (p.Glu559Ala)
c.1895A>C (p.Glu632Ala)
10g.110812457A>GCA213223742RBM20c.2060A>G (p.Glu687Gly)
c.1676A>G (p.Glu559Gly)
c.1895A>G (p.Glu632Gly)
 ClinVar dbSNP gnomAD v2 gnomAD v4
10g.110812457A>TCA378371227RBM20c.2060A>T (p.Glu687Val)
c.1676A>T (p.Glu559Val)
c.1895A>T (p.Glu632Val)
10g.110812458G>ACA471506839RBM20c.2061G>A (p.Glu687=)
c.1677G>A (p.Glu559=)
c.1896G>A (p.Glu632=)
 ClinVar dbSNP
10g.110812458G>CCA378371234RBM20c.2061G>C (p.Glu687Asp)
c.1677G>C (p.Glu559Asp)
c.1896G>C (p.Glu632Asp)
10g.110812458G>TCA378371237RBM20c.2061G>T (p.Glu687Asp)
c.1677G>T (p.Glu559Asp)
c.1896G>T (p.Glu632Asp)
10g.110812459C>ACA471506842RBM20c.2062C>A (p.Arg688=)
c.1678C>A (p.Arg560=)
c.1897C>A (p.Arg633=)
10g.110812459C>GCA378371240RBM20c.2062C>G (p.Arg688Gly)
c.1678C>G (p.Arg560Gly)
c.1897C>G (p.Arg633Gly)
10g.110812459C>TCA335555RBM20c.2062C>T (p.Arg688Ter)
c.1678C>T (p.Arg560Ter)
c.1897C>T (p.Arg633Ter)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.110812460G>ACA5688665RBM20c.2063G>A (p.Arg688Gln)
c.1679G>A (p.Arg560Gln)
c.1898G>A (p.Arg633Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.110812460G>CCA378371250RBM20c.2063G>C (p.Arg688Pro)
c.1679G>C (p.Arg560Pro)
c.1898G>C (p.Arg633Pro)
10g.110812460G>TCA378371251RBM20c.2063G>T (p.Arg688Leu)
c.1679G>T (p.Arg560Leu)
c.1898G>T (p.Arg633Leu)
10g.110812461A>CCA471506844RBM20c.2064A>C (p.Arg688=)
c.1680A>C (p.Arg560=)
c.1899A>C (p.Arg633=)
10g.110812461A>GCA471506846RBM20c.2064A>G (p.Arg688=)
c.1680A>G (p.Arg560=)
c.1899A>G (p.Arg633=)
10g.110812461A>TCA471506850RBM20c.2064A>T (p.Arg688=)
c.1680A>T (p.Arg560=)
c.1899A>T (p.Arg633=)
10g.110812462G>ACA378371252RBM20c.2065G>A (p.Asp689Asn)
c.1681G>A (p.Asp561Asn)
c.1900G>A (p.Asp634Asn)
 ClinVar dbSNP
10g.110812462G>CCA378371253RBM20c.2065G>C (p.Asp689His)
c.1681G>C (p.Asp561His)
c.1900G>C (p.Asp634His)
10g.110812462G>TCA378371256RBM20c.2065G>T (p.Asp689Tyr)
c.1681G>T (p.Asp561Tyr)
c.1900G>T (p.Asp634Tyr)
10g.110812463A>CCA378371265RBM20c.2066A>C (p.Asp689Ala)
c.1682A>C (p.Asp561Ala)
c.1901A>C (p.Asp634Ala)
10g.110812463A>GCA378371268RBM20c.2066A>G (p.Asp689Gly)
c.1682A>G (p.Asp561Gly)
c.1901A>G (p.Asp634Gly)
10g.110812463A>TCA378371274RBM20c.2066A>T (p.Asp689Val)
c.1682A>T (p.Asp561Val)
c.1901A>T (p.Asp634Val)
 gnomAD v4
10g.110812464C>ACA378371276RBM20c.2067C>A (p.Asp689Glu)
c.1683C>A (p.Asp561Glu)
c.1902C>A (p.Asp634Glu)
 ClinVar
10g.110812464C>GCA378371279RBM20c.2067C>G (p.Asp689Glu)
c.1683C>G (p.Asp561Glu)
c.1902C>G (p.Asp634Glu)
10g.110812464C>TCA471506857RBM20c.2067C>T (p.Asp689=)
c.1683C>T (p.Asp561=)
c.1902C>T (p.Asp634=)
 gnomAD v4
10g.110812465C>ACA378371289RBM20c.2068C>A (p.Pro690Thr)
c.1684C>A (p.Pro562Thr)
c.1903C>A (p.Pro635Thr)
 gnomAD v4
10g.110812465C>GCA378371296RBM20c.2068C>G (p.Pro690Ala)
c.1684C>G (p.Pro562Ala)
c.1903C>G (p.Pro635Ala)
10g.110812465C>TCA378371293RBM20c.2068C>T (p.Pro690Ser)
c.1684C>T (p.Pro562Ser)
c.1903C>T (p.Pro635Ser)
 dbSNP gnomAD v4
10g.110812466C>ACA378371298RBM20c.2069C>A (p.Pro690Gln)
c.1685C>A (p.Pro562Gln)
c.1904C>A (p.Pro635Gln)
10g.110812466C>GCA5688666RBM20c.2069C>G (p.Pro690Arg)
c.1685C>G (p.Pro562Arg)
c.1904C>G (p.Pro635Arg)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.110812466C>TCA16605974RBM20c.2069C>T (p.Pro690Leu)
c.1685C>T (p.Pro562Leu)
c.1904C>T (p.Pro635Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.110812467G>ACA213223759RBM20c.2070G>A (p.Pro690=)
c.1686G>A (p.Pro562=)
c.1905G>A (p.Pro635=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.110812467G>CCA471506867RBM20c.2070G>C (p.Pro690=)
c.1686G>C (p.Pro562=)
c.1905G>C (p.Pro635=)
10g.110812467G>TCA471506868RBM20c.2070G>T (p.Pro690=)
c.1686G>T (p.Pro562=)
c.1905G>T (p.Pro635=)
 gnomAD v4
10g.110812468G>ACA378371302RBM20c.2071G>A (p.Ala691Thr)
c.1687G>A (p.Ala563Thr)
c.1906G>A (p.Ala636Thr)
 ClinVar gnomAD v4
10g.110812468G>CCA378371305RBM20c.2071G>C (p.Ala691Pro)
c.1687G>C (p.Ala563Pro)
c.1906G>C (p.Ala636Pro)
10g.110812468G>TCA378371310RBM20c.2071G>T (p.Ala691Ser)
c.1687G>T (p.Ala563Ser)
c.1906G>T (p.Ala636Ser)
 ClinVar dbSNP
10g.110812469C>ACA378371318RBM20c.2072C>A (p.Ala691Asp)
c.1688C>A (p.Ala563Asp)
c.1907C>A (p.Ala636Asp)
10g.110812469C>GCA378371325RBM20c.2072C>G (p.Ala691Gly)
c.1688C>G (p.Ala563Gly)
c.1907C>G (p.Ala636Gly)
10g.110812469C>TCA378371329RBM20c.2072C>T (p.Ala691Val)
c.1688C>T (p.Ala563Val)
c.1907C>T (p.Ala636Val)
 ClinVar dbSNP gnomAD v3 gnomAD v4
10g.110812470T>ACA471506876RBM20c.2073T>A (p.Ala691=)
c.1689T>A (p.Ala563=)
c.1908T>A (p.Ala636=)
10g.110812470T>CCA471506875RBM20c.2073T>C (p.Ala691=)
c.1689T>C (p.Ala563=)
c.1908T>C (p.Ala636=)
10g.110812470T>GCA471506873RBM20c.2073T>G (p.Ala691=)
c.1689T>G (p.Ala563=)
c.1908T>G (p.Ala636=)
10g.110812471C>ACA378371338RBM20c.2074C>A (p.Pro692Thr)
c.1690C>A (p.Pro564Thr)
c.1909C>A (p.Pro637Thr)
10g.110812471C>GCA378371349RBM20c.2074C>G (p.Pro692Ala)
c.1690C>G (p.Pro564Ala)
c.1909C>G (p.Pro637Ala)
10g.110812471C>TCA378371355RBM20c.2074C>T (p.Pro692Ser)
c.1690C>T (p.Pro564Ser)
c.1909C>T (p.Pro637Ser)
10g.110812471_110812472delinsTTCA645568267RBM20c.2074_2075delinsTT (p.Pro692Phe)
c.1690_1691delinsTT (p.Pro564Phe)
c.1909_1910delinsTT (p.Pro637Phe)
 COSMIC
10g.110812472C>ACA378371380RBM20c.2075C>A (p.Pro692His)
c.1691C>A (p.Pro564His)
c.1910C>A (p.Pro637His)
10g.110812472C>GCA378371363RBM20c.2075C>G (p.Pro692Arg)
c.1691C>G (p.Pro564Arg)
c.1910C>G (p.Pro637Arg)
10g.110812472C>TCA378371365RBM20c.2075C>T (p.Pro692Leu)
c.1691C>T (p.Pro564Leu)
c.1910C>T (p.Pro637Leu)
 ClinVar
10g.110812473C>ACA471506880RBM20c.2076C>A (p.Pro692=)
c.1692C>A (p.Pro564=)
c.1911C>A (p.Pro637=)
10g.110812473C>GCA471506883RBM20c.2076C>G (p.Pro692=)
c.1692C>G (p.Pro564=)
c.1911C>G (p.Pro637=)
10g.110812473C>TCA213223762RBM20c.2076C>T (p.Pro692=)
c.1692C>T (p.Pro564=)
c.1911C>T (p.Pro637=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.110812474T>ACA378371382RBM20c.2077T>A (p.Trp693Arg)
c.1693T>A (p.Trp565Arg)
c.1912T>A (p.Trp638Arg)
10g.110812474T>CCA378371383RBM20c.2077T>C (p.Trp693Arg)
c.1693T>C (p.Trp565Arg)
c.1912T>C (p.Trp638Arg)
10g.110812474T>GCA378371387RBM20c.2077T>G (p.Trp693Gly)
c.1693T>G (p.Trp565Gly)
c.1912T>G (p.Trp638Gly)
10g.110812475G>ACA378371390RBM20c.2078G>A (p.Trp693Ter)
c.1694G>A (p.Trp565Ter)
c.1913G>A (p.Trp638Ter)
10g.110812475G>CCA378371393RBM20c.2078G>C (p.Trp693Ser)
c.1694G>C (p.Trp565Ser)
c.1913G>C (p.Trp638Ser)
10g.110812475G>TCA378371404RBM20c.2078G>T (p.Trp693Leu)
c.1694G>T (p.Trp565Leu)
c.1913G>T (p.Trp638Leu)
10g.110812476G>ACA378371412RBM20c.2079G>A (p.Trp693Ter)
c.1695G>A (p.Trp565Ter)
c.1914G>A (p.Trp638Ter)
10g.110812476G>CCA378371418RBM20c.2079G>C (p.Trp693Cys)
c.1695G>C (p.Trp565Cys)
c.1914G>C (p.Trp638Cys)
10g.110812476G>TCA378371426RBM20c.2079G>T (p.Trp693Cys)
c.1695G>T (p.Trp565Cys)
c.1914G>T (p.Trp638Cys)
 gnomAD v4
10g.110812477A>CCA471506891RBM20c.2080A>C (p.Arg694=)
c.1696A>C (p.Arg566=)
c.1915A>C (p.Arg639=)
10g.110812477A>GCA378371431RBM20c.2080A>G (p.Arg694Gly)
c.1696A>G (p.Arg566Gly)
c.1915A>G (p.Arg639Gly)
10g.110812477A>TCA378371436RBM20c.2080A>T (p.Arg694Trp)
c.1696A>T (p.Arg566Trp)
c.1915A>T (p.Arg639Trp)
10g.110812478G>ACA378371449RBM20c.2081G>A (p.Arg694Lys)
c.1697G>A (p.Arg566Lys)
c.1916G>A (p.Arg639Lys)
10g.110812478G>CCA378371448RBM20c.2081G>C (p.Arg694Thr)
c.1697G>C (p.Arg566Thr)
c.1916G>C (p.Arg639Thr)
10g.110812478G>TCA378371439RBM20c.2081G>T (p.Arg694Met)
c.1697G>T (p.Arg566Met)
c.1916G>T (p.Arg639Met)
10g.110812479G>ACA471506895RBM20c.2082G>A (p.Arg694=)
c.1698G>A (p.Arg566=)
c.1917G>A (p.Arg639=)
10g.110812479G>CCA378371452RBM20c.2082G>C (p.Arg694Ser)
c.1698G>C (p.Arg566Ser)
c.1917G>C (p.Arg639Ser)
10g.110812479G>TCA378371457RBM20c.2082G>T (p.Arg694Ser)
c.1698G>T (p.Arg566Ser)
c.1917G>T (p.Arg639Ser)
10g.110812480G>ACA378371461RBM20c.2083G>A (p.Asp695Asn)
c.1699G>A (p.Asp567Asn)
c.1918G>A (p.Asp640Asn)
 gnomAD v4 COSMIC
10g.110812480G>CCA378371469RBM20c.2083G>C (p.Asp695His)
c.1699G>C (p.Asp567His)
c.1918G>C (p.Asp640His)
10g.110812480G>TCA378371472RBM20c.2083G>T (p.Asp695Tyr)
c.1699G>T (p.Asp567Tyr)
c.1918G>T (p.Asp640Tyr)
10g.110812481A>CCA378371475RBM20c.2084A>C (p.Asp695Ala)
c.1700A>C (p.Asp567Ala)
c.1919A>C (p.Asp640Ala)
10g.110812481A>GCA213223767RBM20c.2084A>G (p.Asp695Gly)
c.1700A>G (p.Asp567Gly)
c.1919A>G (p.Asp640Gly)
 ClinVar dbSNP gnomAD v4
10g.110812481A>TCA378371493RBM20c.2084A>T (p.Asp695Val)
c.1700A>T (p.Asp567Val)
c.1919A>T (p.Asp640Val)
10g.110812482C>ACA378371497RBM20c.2085C>A (p.Asp695Glu)
c.1701C>A (p.Asp567Glu)
c.1920C>A (p.Asp640Glu)
10g.110812482C>GCA378371500RBM20c.2085C>G (p.Asp695Glu)
c.1701C>G (p.Asp567Glu)
c.1920C>G (p.Asp640Glu)
 dbSNP
10g.110812482C>TCA471506905RBM20c.2085C>T (p.Asp695=)
c.1701C>T (p.Asp567=)
c.1920C>T (p.Asp640=)
10g.110812483A>CCA378371504RBM20c.2086A>C (p.Asn696His)
c.1702A>C (p.Asn568His)
c.1921A>C (p.Asn641His)
10g.110812483A>GCA378371510RBM20c.2086A>G (p.Asn696Asp)
c.1702A>G (p.Asn568Asp)
c.1921A>G (p.Asn641Asp)
 ClinVar dbSNP
10g.110812483A>TCA378371514RBM20c.2086A>T (p.Asn696Tyr)
c.1702A>T (p.Asn568Tyr)
c.1921A>T (p.Asn641Tyr)
10g.110812484A>CCA378371530RBM20c.2087A>C (p.Asn696Thr)
c.1703A>C (p.Asn568Thr)
c.1922A>C (p.Asn641Thr)
 dbSNP
10g.110812484A>GCA378371521RBM20c.2087A>G (p.Asn696Ser)
c.1703A>G (p.Asn568Ser)
c.1922A>G (p.Asn641Ser)
 ClinVar dbSNP
10g.110812484A>TCA378371524RBM20c.2087A>T (p.Asn696Ile)
c.1703A>T (p.Asn568Ile)
c.1922A>T (p.Asn641Ile)
10g.110812485delCA932526619RBM20c.2088del (p.Asn696LysfsTer?)
c.1704del (p.Asn568LysfsTer?)
c.1923del (p.Asn641LysfsTer?)
 dbSNP
10g.110812485C>ACA378371533RBM20c.2088C>A (p.Asn696Lys)
c.1704C>A (p.Asn568Lys)
c.1923C>A (p.Asn641Lys)
10g.110812485C>GCA378371542RBM20c.2088C>G (p.Asn696Lys)
c.1704C>G (p.Asn568Lys)
c.1923C>G (p.Asn641Lys)
10g.110812485C>TCA471506917RBM20c.2088C>T (p.Asn696=)
c.1704C>T (p.Asn568=)
c.1923C>T (p.Asn641=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
10g.110812486G>ACA346597RBM20c.2089G>A (p.Gly697Arg)
c.1705G>A (p.Gly569Arg)
c.1924G>A (p.Gly642Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.110812486G>CCA378371548RBM20c.2089G>C (p.Gly697Arg)
c.1705G>C (p.Gly569Arg)
c.1924G>C (p.Gly642Arg)
10g.110812486G>TCA378371550RBM20c.2089G>T (p.Gly697Ter)
c.1705G>T (p.Gly569Ter)
c.1924G>T (p.Gly642Ter)
 gnomAD v4
10g.110812487G>ACA378371553RBM20c.2090G>A (p.Gly697Glu)
c.1706G>A (p.Gly569Glu)
c.1925G>A (p.Gly642Glu)
10g.110812487G>CCA378371558RBM20c.2090G>C (p.Gly697Ala)
c.1706G>C (p.Gly569Ala)
c.1925G>C (p.Gly642Ala)
10g.110812487G>TCA378371563RBM20c.2090G>T (p.Gly697Val)
c.1706G>T (p.Gly569Val)
c.1925G>T (p.Gly642Val)
10g.110812488A>CCA471506925RBM20c.2091A>C (p.Gly697=)
c.1707A>C (p.Gly569=)
c.1926A>C (p.Gly642=)
10g.110812488A>GCA471506928RBM20c.2091A>G (p.Gly697=)
c.1707A>G (p.Gly569=)
c.1926A>G (p.Gly642=)
10g.110812488A>TCA471506929RBM20c.2091A>T (p.Gly697=)
c.1707A>T (p.Gly569=)
c.1926A>T (p.Gly642=)
10g.110812489G>ACA378371568RBM20c.2092G>A (p.Asp698Asn)
c.1708G>A (p.Asp570Asn)
c.1927G>A (p.Asp643Asn)
 COSMIC
10g.110812489G>CCA378371570RBM20c.2092G>C (p.Asp698His)
c.1708G>C (p.Asp570His)
c.1927G>C (p.Asp643His)
10g.110812489G>TCA378371573RBM20c.2092G>T (p.Asp698Tyr)
c.1708G>T (p.Asp570Tyr)
c.1927G>T (p.Asp643Tyr)
10g.110812490A>CCA378371576RBM20c.2093A>C (p.Asp698Ala)
c.1709A>C (p.Asp570Ala)
c.1928A>C (p.Asp643Ala)
10g.110812490A>GCA378371575RBM20c.2093A>G (p.Asp698Gly)
c.1709A>G (p.Asp570Gly)
c.1928A>G (p.Asp643Gly)
10g.110812490A>TCA378371574RBM20c.2093A>T (p.Asp698Val)
c.1709A>T (p.Asp570Val)
c.1928A>T (p.Asp643Val)
 dbSNP gnomAD v3 gnomAD v4
10g.110812491T>ACA378371580RBM20c.2094T>A (p.Asp698Glu)
c.1710T>A (p.Asp570Glu)
c.1929T>A (p.Asp643Glu)
 dbSNP gnomAD v3 gnomAD v4
10g.110812491T>CCA471506935RBM20c.2094T>C (p.Asp698=)
c.1710T>C (p.Asp570=)
c.1929T>C (p.Asp643=)
10g.110812491T>GCA378371584RBM20c.2094T>G (p.Asp698Glu)
c.1710T>G (p.Asp570Glu)
c.1929T>G (p.Asp643Glu)
10g.110812492G>ACA213223780RBM20c.2095G>A (p.Asp699Asn)
c.1711G>A (p.Asp571Asn)
c.1930G>A (p.Asp644Asn)
 dbSNP
10g.110812492G>CCA378371600RBM20c.2095G>C (p.Asp699His)
c.1711G>C (p.Asp571His)
c.1930G>C (p.Asp644His)
10g.110812492G>TCA378371597RBM20c.2095G>T (p.Asp699Tyr)
c.1711G>T (p.Asp571Tyr)
c.1930G>T (p.Asp644Tyr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.110812493A>CCA378371610RBM20c.2096A>C (p.Asp699Ala)
c.1712A>C (p.Asp571Ala)
c.1931A>C (p.Asp644Ala)
10g.110812493A>GCA378371614RBM20c.2096A>G (p.Asp699Gly)
c.1712A>G (p.Asp571Gly)
c.1931A>G (p.Asp644Gly)
 dbSNP gnomAD v2 gnomAD v4
10g.110812493A>TCA378371613RBM20c.2096A>T (p.Asp699Val)
c.1712A>T (p.Asp571Val)
c.1931A>T (p.Asp644Val)
10g.110812494C>ACA378371618RBM20c.2097C>A (p.Asp699Glu)
c.1713C>A (p.Asp571Glu)
c.1932C>A (p.Asp644Glu)
10g.110812494C>GCA378371647RBM20c.2097C>G (p.Asp699Glu)
c.1713C>G (p.Asp571Glu)
c.1932C>G (p.Asp644Glu)
10g.110812494C>TCA5688667RBM20c.2097C>T (p.Asp699=)
c.1713C>T (p.Asp571=)
c.1932C>T (p.Asp644=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.110812495A>CCA378371652RBM20c.2098A>C (p.Lys700Gln)
c.1714A>C (p.Lys572Gln)
c.1933A>C (p.Lys645Gln)
10g.110812495A>GCA378371660RBM20c.2098A>G (p.Lys700Glu)
c.1714A>G (p.Lys572Glu)
c.1933A>G (p.Lys645Glu)
10g.110812495A>TCA378371657RBM20c.2098A>T (p.Lys700Ter)
c.1714A>T (p.Lys572Ter)
c.1933A>T (p.Lys645Ter)
10g.110812495_110812496delCA2610892816RBM20c.2098_2099del (p.Lys700GlufsTer10)
c.1714_1715del (p.Lys572GlufsTer10)
c.1933_1934del (p.Lys645GlufsTer10)
 gnomAD v4
10g.110812496A>CCA378371677RBM20c.2099A>C (p.Lys700Thr)
c.1715A>C (p.Lys572Thr)
c.1934A>C (p.Lys645Thr)
10g.110812496A>GCA378371693RBM20c.2099A>G (p.Lys700Arg)
c.1715A>G (p.Lys572Arg)
c.1934A>G (p.Lys645Arg)
 dbSNP gnomAD v3 gnomAD v4
10g.110812496A>TCA378371685RBM20c.2099A>T (p.Lys700Met)
c.1715A>T (p.Lys572Met)
c.1934A>T (p.Lys645Met)
10g.110812497G>ACA471506949RBM20c.2100G>A (p.Lys700=)
c.1716G>A (p.Lys572=)
c.1935G>A (p.Lys645=)
 ClinVar
10g.110812497G>CCA213223783RBM20c.2100G>C (p.Lys700Asn)
c.1716G>C (p.Lys572Asn)
c.1935G>C (p.Lys645Asn)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.110812497G>TCA378371698RBM20c.2100G>T (p.Lys700Asn)
c.1716G>T (p.Lys572Asn)
c.1935G>T (p.Lys645Asn)
10g.110812498A>CCA471506953RBM20c.2101A>C (p.Arg701=)
c.1717A>C (p.Arg573=)
c.1936A>C (p.Arg646=)
10g.110812498A>GCA378371704RBM20c.2101A>G (p.Arg701Gly)
c.1717A>G (p.Arg573Gly)
c.1936A>G (p.Arg646Gly)
10g.110812498A>TCA378371708RBM20c.2101A>T (p.Arg701Trp)
c.1717A>T (p.Arg573Trp)
c.1936A>T (p.Arg646Trp)
10g.110812499G>ACA378371720RBM20c.2102G>A (p.Arg701Lys)
c.1718G>A (p.Arg573Lys)
c.1937G>A (p.Arg646Lys)
 ClinVar gnomAD v4
10g.110812499G>CCA378371733RBM20c.2102G>C (p.Arg701Thr)
c.1718G>C (p.Arg573Thr)
c.1937G>C (p.Arg646Thr)
10g.110812499G>TCA378371741RBM20c.2102G>T (p.Arg701Met)
c.1718G>T (p.Arg573Met)
c.1937G>T (p.Arg646Met)
10g.110812500G>ACA471506962RBM20c.2103G>A (p.Arg701=)
c.1719G>A (p.Arg573=)
c.1938G>A (p.Arg646=)
 gnomAD v4
10g.110812500G>CCA378371754RBM20c.2103G>C (p.Arg701Ser)
c.1719G>C (p.Arg573Ser)
c.1938G>C (p.Arg646Ser)
10g.110812500G>TCA378371757RBM20c.2103G>T (p.Arg701Ser)
c.1719G>T (p.Arg573Ser)
c.1938G>T (p.Arg646Ser)
10g.110812501G>ACA378371762RBM20c.2104G>A (p.Asp702Asn)
c.1720G>A (p.Asp574Asn)
c.1939G>A (p.Asp647Asn)
10g.110812501G>CCA378371770RBM20c.2104G>C (p.Asp702His)
c.1720G>C (p.Asp574His)
c.1939G>C (p.Asp647His)
10g.110812501G>TCA378371773RBM20c.2104G>T (p.Asp702Tyr)
c.1720G>T (p.Asp574Tyr)
c.1939G>T (p.Asp647Tyr)
 dbSNP gnomAD v2 gnomAD v4
10g.110812502A>CCA378371777RBM20c.2105A>C (p.Asp702Ala)
c.1721A>C (p.Asp574Ala)
c.1940A>C (p.Asp647Ala)
10g.110812502A>GCA378371784RBM20c.2105A>G (p.Asp702Gly)
c.1721A>G (p.Asp574Gly)
c.1940A>G (p.Asp647Gly)
10g.110812502A>TCA378371780RBM20c.2105A>T (p.Asp702Val)
c.1721A>T (p.Asp574Val)
c.1940A>T (p.Asp647Val)
10g.110812503C>ACA378371786RBM20c.2106C>A (p.Asp702Glu)
c.1722C>A (p.Asp574Glu)
c.1941C>A (p.Asp647Glu)
10g.110812503C>GCA378371787RBM20c.2106C>G (p.Asp702Glu)
c.1722C>G (p.Asp574Glu)
c.1941C>G (p.Asp647Glu)
 ClinVar
10g.110812503C>TCA471506968RBM20c.2106C>T (p.Asp702=)
c.1722C>T (p.Asp574=)
c.1941C>T (p.Asp647=)
10g.110812504A>CCA471506969RBM20c.2107A>C (p.Arg703=)
c.1723A>C (p.Arg575=)
c.1942A>C (p.Arg648=)
10g.110812504A>GCA213223787RBM20c.2107A>G (p.Arg703Gly)
c.1723A>G (p.Arg575Gly)
c.1942A>G (p.Arg648Gly)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.110812504A>TCA378371795RBM20c.2107A>T (p.Arg703Trp)
c.1723A>T (p.Arg575Trp)
c.1942A>T (p.Arg648Trp)
10g.110812505G>ACA133301RBM20c.2108G>A (p.Arg703Lys)
c.1724G>A (p.Arg575Lys)
c.1943G>A (p.Arg648Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.110812505G>CCA378371803RBM20c.2108G>C (p.Arg703Thr)
c.1724G>C (p.Arg575Thr)
c.1943G>C (p.Arg648Thr)
10g.110812505G>TCA378371810RBM20c.2108G>T (p.Arg703Met)
c.1724G>T (p.Arg575Met)
c.1943G>T (p.Arg648Met)
10g.110812506G>ACA471506977RBM20c.2109G>A (p.Arg703=)
c.1725G>A (p.Arg575=)
c.1944G>A (p.Arg648=)
10g.110812506G>CCA213223788RBM20c.2109G>C (p.Arg703Ser)
c.1725G>C (p.Arg575Ser)
c.1944G>C (p.Arg648Ser)
 ClinVar dbSNP gnomAD v3 gnomAD v4
10g.110812506G>TCA378371819RBM20c.2109G>T (p.Arg703Ser)
c.1725G>T (p.Arg575Ser)
c.1944G>T (p.Arg648Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.110812507A>CCA378371832RBM20c.2110A>C (p.Met704Leu)
c.1726A>C (p.Met576Leu)
c.1945A>C (p.Met649Leu)
 gnomAD v4
10g.110812507A>GCA378371827RBM20c.2110A>G (p.Met704Val)
c.1726A>G (p.Met576Val)
c.1945A>G (p.Met649Val)
 dbSNP
10g.110812507A>TCA378371822RBM20c.2110A>T (p.Met704Leu)
c.1726A>T (p.Met576Leu)
c.1945A>T (p.Met649Leu)
 gnomAD v4
10g.110812508T>ACA378371835RBM20c.2111T>A (p.Met704Lys)
c.1727T>A (p.Met576Lys)
c.1946T>A (p.Met649Lys)
 gnomAD v4
10g.110812508T>CCA378371837RBM20c.2111T>C (p.Met704Thr)
c.1727T>C (p.Met576Thr)
c.1946T>C (p.Met649Thr)
 dbSNP
10g.110812508T>GCA378371838RBM20c.2111T>G (p.Met704Arg)
c.1727T>G (p.Met576Arg)
c.1946T>G (p.Met649Arg)
10g.110812509G>ACA378371842RBM20c.2112G>A (p.Met704Ile)
c.1728G>A (p.Met576Ile)
c.1947G>A (p.Met649Ile)
 COSMIC
10g.110812509G>CCA378371853RBM20c.2112G>C (p.Met704Ile)
c.1728G>C (p.Met576Ile)
c.1947G>C (p.Met649Ile)
10g.110812509G>TCA378371861RBM20c.2112G>T (p.Met704Ile)
c.1728G>T (p.Met576Ile)
c.1947G>T (p.Met649Ile)
10g.110812510G>ACA213223789RBM20c.2113G>A (p.Asp705Asn)
c.1729G>A (p.Asp577Asn)
c.1948G>A (p.Asp650Asn)
 ClinVar dbSNP gnomAD v4
10g.110812510G>CCA378371874RBM20c.2113G>C (p.Asp705His)
c.1729G>C (p.Asp577His)
c.1948G>C (p.Asp650His)
10g.110812510G>TCA378371879RBM20c.2113G>T (p.Asp705Tyr)
c.1729G>T (p.Asp577Tyr)
c.1948G>T (p.Asp650Tyr)
10g.110812511A>CCA378371881RBM20c.2114A>C (p.Asp705Ala)
c.1730A>C (p.Asp577Ala)
c.1949A>C (p.Asp650Ala)
10g.110812511A>GCA378371883RBM20c.2114A>G (p.Asp705Gly)
c.1730A>G (p.Asp577Gly)
c.1949A>G (p.Asp650Gly)
10g.110812511A>TCA378371885RBM20c.2114A>T (p.Asp705Val)
c.1730A>T (p.Asp577Val)
c.1949A>T (p.Asp650Val)
 dbSNP
10g.110812512C>ACA378371891RBM20c.2115C>A (p.Asp705Glu)
c.1731C>A (p.Asp577Glu)
c.1950C>A (p.Asp650Glu)
 ClinVar dbSNP gnomAD v2 gnomAD v4
10g.110812512C>GCA378371889RBM20c.2115C>G (p.Asp705Glu)
c.1731C>G (p.Asp577Glu)
c.1950C>G (p.Asp650Glu)
10g.110812512C>TCA471506990RBM20c.2115C>T (p.Asp705=)
c.1731C>T (p.Asp577=)
c.1950C>T (p.Asp650=)
10g.110812513C>ACA335516RBM20c.2116C>A (p.Pro706Thr)
c.1732C>A (p.Pro578Thr)
c.1951C>A (p.Pro651Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.110812513C>GCA378371893RBM20c.2116C>G (p.Pro706Ala)
c.1732C>G (p.Pro578Ala)
c.1951C>G (p.Pro651Ala)
10g.110812513C>TCA378371896RBM20c.2116C>T (p.Pro706Ser)
c.1732C>T (p.Pro578Ser)
c.1951C>T (p.Pro651Ser)
 gnomAD v4
10g.110812514C>ACA378371899RBM20c.2117C>A (p.Pro706His)
c.1733C>A (p.Pro578His)
c.1952C>A (p.Pro651His)
10g.110812514C>GCA378371902RBM20c.2117C>G (p.Pro706Arg)
c.1733C>G (p.Pro578Arg)
c.1952C>G (p.Pro651Arg)
 dbSNP gnomAD v3 gnomAD v4
10g.110812514C>TCA378371914RBM20c.2117C>T (p.Pro706Leu)
c.1733C>T (p.Pro578Leu)
c.1952C>T (p.Pro651Leu)
10g.110812515C>ACA471506999RBM20c.2118C>A (p.Pro706=)
c.1734C>A (p.Pro578=)
c.1953C>A (p.Pro651=)
10g.110812515C>GCA471507000RBM20c.2118C>G (p.Pro706=)
c.1734C>G (p.Pro578=)
c.1953C>G (p.Pro651=)
10g.110812515C>TCA471507001RBM20c.2118C>T (p.Pro706=)
c.1734C>T (p.Pro578=)
c.1953C>T (p.Pro651=)
 ClinVar dbSNP
10g.110812516T>ACA378371941RBM20c.2119T>A (p.Trp707Arg)
c.1735T>A (p.Trp579Arg)
c.1954T>A (p.Trp652Arg)
 ClinVar dbSNP gnomAD v4
10g.110812516T>CCA378371945RBM20c.2119T>C (p.Trp707Arg)
c.1735T>C (p.Trp579Arg)
c.1954T>C (p.Trp652Arg)
 ClinVar
10g.110812516T>GCA378371946RBM20c.2119T>G (p.Trp707Gly)
c.1735T>G (p.Trp579Gly)
c.1954T>G (p.Trp652Gly)
10g.110812517G>ACA378371947RBM20c.2120G>A (p.Trp707Ter)
c.1736G>A (p.Trp579Ter)
c.1955G>A (p.Trp652Ter)
10g.110812517G>CCA378371951RBM20c.2120G>C (p.Trp707Ser)
c.1736G>C (p.Trp579Ser)
c.1955G>C (p.Trp652Ser)
10g.110812517G>TCA378371955RBM20c.2120G>T (p.Trp707Leu)
c.1736G>T (p.Trp579Leu)
c.1955G>T (p.Trp652Leu)
10g.110812518G>ACA378371969RBM20c.2121G>A (p.Trp707Ter)
c.1737G>A (p.Trp579Ter)
c.1956G>A (p.Trp652Ter)
10g.110812518G>CCA378371967RBM20c.2121G>C (p.Trp707Cys)
c.1737G>C (p.Trp579Cys)
c.1956G>C (p.Trp652Cys)
10g.110812518G>TCA378371960RBM20c.2121G>T (p.Trp707Cys)
c.1737G>T (p.Trp579Cys)
c.1956G>T (p.Trp652Cys)
10g.110812519G>ACA378371972RBM20c.2122G>A (p.Ala708Thr)
c.1738G>A (p.Ala580Thr)
c.1957G>A (p.Ala653Thr)
10g.110812519G>CCA378371993RBM20c.2122G>C (p.Ala708Pro)
c.1738G>C (p.Ala580Pro)
c.1957G>C (p.Ala653Pro)
10g.110812519G>TCA378371983RBM20c.2122G>T (p.Ala708Ser)
c.1738G>T (p.Ala580Ser)
c.1957G>T (p.Ala653Ser)
10g.110812520C>ACA378371997RBM20c.2123C>A (p.Ala708Glu)
c.1739C>A (p.Ala580Glu)
c.1958C>A (p.Ala653Glu)
 dbSNP
10g.110812520C>GCA5688668RBM20c.2123C>G (p.Ala708Gly)
c.1739C>G (p.Ala580Gly)
c.1958C>G (p.Ala653Gly)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.110812520C>TCA378371998RBM20c.2123C>T (p.Ala708Val)
c.1739C>T (p.Ala580Val)
c.1958C>T (p.Ala653Val)
 gnomAD v4
10g.110812521A>CCA471507008RBM20c.2124A>C (p.Ala708=)
c.1740A>C (p.Ala580=)
c.1959A>C (p.Ala653=)
10g.110812521A>GCA471507009RBM20c.2124A>G (p.Ala708=)
c.1740A>G (p.Ala580=)
c.1959A>G (p.Ala653=)
10g.110812521A>TCA471507010RBM20c.2124A>T (p.Ala708=)
c.1740A>T (p.Ala580=)
c.1959A>T (p.Ala653=)
 gnomAD v4
10g.110812522C>ACA378371999RBM20c.2125C>A (p.His709Asn)
c.1741C>A (p.His581Asn)
c.1960C>A (p.His654Asn)
10g.110812522C>GCA378372003RBM20c.2125C>G (p.His709Asp)
c.1741C>G (p.His581Asp)
c.1960C>G (p.His654Asp)
10g.110812522C>TCA378372013RBM20c.2125C>T (p.His709Tyr)
c.1741C>T (p.His581Tyr)
c.1960C>T (p.His654Tyr)
10g.110812523A>CCA378372018RBM20c.2126A>C (p.His709Pro)
c.1742A>C (p.His581Pro)
c.1961A>C (p.His654Pro)
10g.110812523A>GCA378372025RBM20c.2126A>G (p.His709Arg)
c.1742A>G (p.His581Arg)
c.1961A>G (p.His654Arg)
 ClinVar dbSNP gnomAD v4
10g.110812523A>TCA378372046RBM20c.2126A>T (p.His709Leu)
c.1742A>T (p.His581Leu)
c.1961A>T (p.His654Leu)
10g.110812524T>ACA378372055RBM20c.2127T>A (p.His709Gln)
c.1743T>A (p.His581Gln)
c.1962T>A (p.His654Gln)
10g.110812524T>CCA471507018RBM20c.2127T>C (p.His709=)
c.1743T>C (p.His581=)
c.1962T>C (p.His654=)
10g.110812524T>GCA378372059RBM20c.2127T>G (p.His709Gln)
c.1743T>G (p.His581Gln)
c.1962T>G (p.His654Gln)
10g.110812525G>ACA378372062RBM20c.2128G>A (p.Asp710Asn)
c.1744G>A (p.Asp582Asn)
c.1963G>A (p.Asp655Asn)
10g.110812525G>CCA378372061RBM20c.2128G>C (p.Asp710His)
c.1744G>C (p.Asp582His)
c.1963G>C (p.Asp655His)
10g.110812525G>TCA378372060RBM20c.2128G>T (p.Asp710Tyr)
c.1744G>T (p.Asp582Tyr)
c.1963G>T (p.Asp655Tyr)
10g.110812526A>CCA378372065RBM20c.2129A>C (p.Asp710Ala)
c.1745A>C (p.Asp582Ala)
c.1964A>C (p.Asp655Ala)
10g.110812526A>GCA378372068RBM20c.2129A>G (p.Asp710Gly)
c.1745A>G (p.Asp582Gly)
c.1964A>G (p.Asp655Gly)
 gnomAD v4
10g.110812526A>TCA378372076RBM20c.2129A>T (p.Asp710Val)
c.1745A>T (p.Asp582Val)
c.1964A>T (p.Asp655Val)
10g.110812527T>ACA378372083RBM20c.2130T>A (p.Asp710Glu)
c.1746T>A (p.Asp582Glu)
c.1965T>A (p.Asp655Glu)
10g.110812527T>CCA471507027RBM20c.2130T>C (p.Asp710=)
c.1746T>C (p.Asp582=)
c.1965T>C (p.Asp655=)
 dbSNP gnomAD v2 gnomAD v4
10g.110812527T>GCA378372086RBM20c.2130T>G (p.Asp710Glu)
c.1746T>G (p.Asp582Glu)
c.1965T>G (p.Asp655Glu)
10g.110812528C>ACA378372087RBM20c.2131C>A (p.Arg711Ser)
c.1747C>A (p.Arg583Ser)
c.1966C>A (p.Arg656Ser)
10g.110812528C>GCA378372089RBM20c.2131C>G (p.Arg711Gly)
c.1747C>G (p.Arg583Gly)
c.1966C>G (p.Arg656Gly)
 ClinVar dbSNP
10g.110812528C>TCA10587690RBM20c.2131C>T (p.Arg711Cys)
c.1747C>T (p.Arg583Cys)
c.1966C>T (p.Arg656Cys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.110812529G>ACA378372098RBM20c.2132G>A (p.Arg711His)
c.1748G>A (p.Arg583His)
c.1967G>A (p.Arg656His)
 ClinVar dbSNP
10g.110812529G>CCA378372114RBM20c.2132G>C (p.Arg711Pro)
c.1748G>C (p.Arg583Pro)
c.1967G>C (p.Arg656Pro)
 ClinVar dbSNP
10g.110812529G>TCA378372118RBM20c.2132G>T (p.Arg711Leu)
c.1748G>T (p.Arg583Leu)
c.1967G>T (p.Arg656Leu)
 gnomAD v4
10g.110812530C>ACA471507032RBM20c.2133C>A (p.Arg711=)
c.1749C>A (p.Arg583=)
c.1968C>A (p.Arg656=)
10g.110812530C>GCA471507035RBM20c.2133C>G (p.Arg711=)
c.1749C>G (p.Arg583=)
c.1968C>G (p.Arg656=)
10g.110812530C>TCA471507036RBM20c.2133C>T (p.Arg711=)
c.1749C>T (p.Arg583=)
c.1968C>T (p.Arg656=)
 gnomAD v4
10g.110812531A>CCA378372123RBM20c.2134A>C (p.Lys712Gln)
c.1750A>C (p.Lys584Gln)
c.1969A>C (p.Lys657Gln)
10g.110812531A>GCA378372122RBM20c.2134A>G (p.Lys712Glu)
c.1750A>G (p.Lys584Glu)
c.1969A>G (p.Lys657Glu)
10g.110812531A>TCA378372121RBM20c.2134A>T (p.Lys712Ter)
c.1750A>T (p.Lys584Ter)
c.1969A>T (p.Lys657Ter)

Number of alleles fetched