Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.108209145T>ACA388613976LIG4c.1923A>T (p.Arg641Ser)
c.2124A>T (p.Arg708Ser)
c.2160A>T (p.Arg720Ser)
c.2136A>T (p.Arg712Ser)
13g.108209145T>CCA484975311LIG4c.1923A>G (p.Arg641=)
c.2124A>G (p.Arg708=)
c.2160A>G (p.Arg720=)
c.2136A>G (p.Arg712=)
13g.108209145T>GCA388613977LIG4c.1923A>C (p.Arg641Ser)
c.2124A>C (p.Arg708Ser)
c.2160A>C (p.Arg720Ser)
c.2136A>C (p.Arg712Ser)
13g.108209146C>ACA388613978LIG4c.1922G>T (p.Arg641Ile)
c.2123G>T (p.Arg708Ile)
c.2159G>T (p.Arg720Ile)
c.2135G>T (p.Arg712Ile)
13g.108209146C=CA2117794063LIG4c.1922G= (p.Arg641=)
c.2123G= (p.Arg708=)
c.2159G= (p.Arg720=)
c.2135G= (p.Arg712=)
13g.108209146C>GCA388613979LIG4c.1922G>C (p.Arg641Thr)
c.2123G>C (p.Arg708Thr)
c.2159G>C (p.Arg720Thr)
c.2135G>C (p.Arg712Thr)
13g.108209146C>TCA388613980LIG4c.1922G>A (p.Arg641Lys)
c.2123G>A (p.Arg708Lys)
c.2159G>A (p.Arg720Lys)
c.2135G>A (p.Arg712Lys)
13g.108209147T>ACA388613982LIG4c.1921A>T (p.Arg641Ter)
c.2122A>T (p.Arg708Ter)
c.2158A>T (p.Arg720Ter)
c.2134A>T (p.Arg712Ter)
13g.108209147T>CCA388613981LIG4c.1921A>G (p.Arg641Gly)
c.2122A>G (p.Arg708Gly)
c.2158A>G (p.Arg720Gly)
c.2134A>G (p.Arg712Gly)
13g.108209147T>GCA484975317LIG4c.1921A>C (p.Arg641=)
c.2122A>C (p.Arg708=)
c.2158A>C (p.Arg720=)
c.2134A>C (p.Arg712=)
13g.108209147dupCA7043556LIG4c.1921dup (p.Arg641LysfsTer10)
c.2122dup (p.Arg708LysfsTer10)
c.2158dup (p.Arg720LysfsTer10)
c.2134dup (p.Arg712LysfsTer10)
 dbSNP ExAC gnomAD v2
13g.108209148G>ACA484975319LIG4c.1920C>T (p.Ile640=)
c.2121C>T (p.Ile707=)
c.2157C>T (p.Ile719=)
c.2133C>T (p.Ile711=)
13g.108209148G>CCA388613983LIG4c.1920C>G (p.Ile640Met)
c.2121C>G (p.Ile707Met)
c.2157C>G (p.Ile719Met)
c.2133C>G (p.Ile711Met)
13g.108209148G>TCA484975320LIG4c.1920C>A (p.Ile640=)
c.2121C>A (p.Ile707=)
c.2157C>A (p.Ile719=)
c.2133C>A (p.Ile711=)
13g.108209149A>CCA388613984LIG4c.1919T>G (p.Ile640Ser)
c.2120T>G (p.Ile707Ser)
c.2156T>G (p.Ile719Ser)
c.2132T>G (p.Ile711Ser)
13g.108209149A>GCA388613985LIG4c.1919T>C (p.Ile640Thr)
c.2120T>C (p.Ile707Thr)
c.2156T>C (p.Ile719Thr)
c.2132T>C (p.Ile711Thr)
13g.108209149A>TCA388613986LIG4c.1919T>A (p.Ile640Asn)
c.2120T>A (p.Ile707Asn)
c.2156T>A (p.Ile719Asn)
c.2132T>A (p.Ile711Asn)
13g.108209150T>ACA7043557LIG4c.1918A>T (p.Ile640Phe)
c.2119A>T (p.Ile707Phe)
c.2155A>T (p.Ile719Phe)
c.2131A>T (p.Ile711Phe)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.108209150T>CCA388613987LIG4c.1918A>G (p.Ile640Val)
c.2119A>G (p.Ile707Val)
c.2155A>G (p.Ile719Val)
c.2131A>G (p.Ile711Val)
 gnomAD v4
13g.108209150T>GCA388613988LIG4c.1918A>C (p.Ile640Leu)
c.2119A>C (p.Ile707Leu)
c.2155A>C (p.Ile719Leu)
c.2131A>C (p.Ile711Leu)
13g.108209150T=CA2117794064LIG4c.1918A= (p.Ile640=)
c.2119A= (p.Ile707=)
c.2155A= (p.Ile719=)
c.2131A= (p.Ile711=)
13g.108209151G>ACA484975328LIG4c.1917C>T (p.Asn639=)
c.2118C>T (p.Asn706=)
c.2154C>T (p.Asn718=)
c.2130C>T (p.Asn710=)
 ClinVar
13g.108209151G>CCA388613989LIG4c.1917C>G (p.Asn639Lys)
c.2118C>G (p.Asn706Lys)
c.2154C>G (p.Asn718Lys)
c.2130C>G (p.Asn710Lys)
13g.108209151G>TCA388613990LIG4c.1917C>A (p.Asn639Lys)
c.2118C>A (p.Asn706Lys)
c.2154C>A (p.Asn718Lys)
c.2130C>A (p.Asn710Lys)
13g.108209152T>ACA388613991LIG4c.1916A>T (p.Asn639Ile)
c.2117A>T (p.Asn706Ile)
c.2153A>T (p.Asn718Ile)
c.2129A>T (p.Asn710Ile)
13g.108209152T>CCA388613992LIG4c.1916A>G (p.Asn639Ser)
c.2117A>G (p.Asn706Ser)
c.2153A>G (p.Asn718Ser)
c.2129A>G (p.Asn710Ser)
13g.108209152T>GCA388613993LIG4c.1916A>C (p.Asn639Thr)
c.2117A>C (p.Asn706Thr)
c.2153A>C (p.Asn718Thr)
c.2129A>C (p.Asn710Thr)
13g.108209153T>ACA388613994LIG4c.1915A>T (p.Asn639Tyr)
c.2116A>T (p.Asn706Tyr)
c.2152A>T (p.Asn718Tyr)
c.2128A>T (p.Asn710Tyr)
13g.108209153T>CCA388613995LIG4c.1915A>G (p.Asn639Asp)
c.2116A>G (p.Asn706Asp)
c.2152A>G (p.Asn718Asp)
c.2128A>G (p.Asn710Asp)
13g.108209153T>GCA388613996LIG4c.1915A>C (p.Asn639His)
c.2116A>C (p.Asn706His)
c.2152A>C (p.Asn718His)
c.2128A>C (p.Asn710His)
13g.108209154C>ACA388613997LIG4c.1914G>T (p.Glu638Asp)
c.2115G>T (p.Glu705Asp)
c.2151G>T (p.Glu717Asp)
c.2127G>T (p.Glu709Asp)
13g.108209154C>GCA388613998LIG4c.1914G>C (p.Glu638Asp)
c.2115G>C (p.Glu705Asp)
c.2151G>C (p.Glu717Asp)
c.2127G>C (p.Glu709Asp)
13g.108209154C>TCA484975333LIG4c.1914G>A (p.Glu638=)
c.2115G>A (p.Glu705=)
c.2151G>A (p.Glu717=)
c.2127G>A (p.Glu709=)
13g.108209155T>ACA388613999LIG4c.1913A>T (p.Glu638Val)
c.2114A>T (p.Glu705Val)
c.2150A>T (p.Glu717Val)
c.2126A>T (p.Glu709Val)
13g.108209155T>CCA388614000LIG4c.1913A>G (p.Glu638Gly)
c.2114A>G (p.Glu705Gly)
c.2150A>G (p.Glu717Gly)
c.2126A>G (p.Glu709Gly)
13g.108209155T>GCA388614001LIG4c.1913A>C (p.Glu638Ala)
c.2114A>C (p.Glu705Ala)
c.2150A>C (p.Glu717Ala)
c.2126A>C (p.Glu709Ala)
13g.108209156C>ACA388614002LIG4c.1912G>T (p.Glu638Ter)
c.2113G>T (p.Glu705Ter)
c.2149G>T (p.Glu717Ter)
c.2125G>T (p.Glu709Ter)
13g.108209156C=CA2117794065LIG4c.1912G= (p.Glu638=)
c.2113G= (p.Glu705=)
c.2149G= (p.Glu717=)
c.2125G= (p.Glu709=)
13g.108209156C>GCA388614004LIG4c.1912G>C (p.Glu638Gln)
c.2113G>C (p.Glu705Gln)
c.2149G>C (p.Glu717Gln)
c.2125G>C (p.Glu709Gln)
13g.108209156C>TCA388614003LIG4c.1912G>A (p.Glu638Lys)
c.2113G>A (p.Glu705Lys)
c.2149G>A (p.Glu717Lys)
c.2125G>A (p.Glu709Lys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.108209157A>CCA484975335LIG4c.1911T>G (p.Ser637=)
c.2112T>G (p.Ser704=)
c.2148T>G (p.Ser716=)
c.2124T>G (p.Ser708=)
13g.108209157A>GCA484975337LIG4c.1911T>C (p.Ser637=)
c.2112T>C (p.Ser704=)
c.2148T>C (p.Ser716=)
c.2124T>C (p.Ser708=)
 gnomAD v4
13g.108209157A>TCA484975338LIG4c.1911T>A (p.Ser637=)
c.2112T>A (p.Ser704=)
c.2148T>A (p.Ser716=)
c.2124T>A (p.Ser708=)
13g.108209158G>ACA388614005LIG4c.1910C>T (p.Ser637Phe)
c.2111C>T (p.Ser704Phe)
c.2147C>T (p.Ser716Phe)
c.2123C>T (p.Ser708Phe)
13g.108209158G>CCA388614006LIG4c.1910C>G (p.Ser637Cys)
c.2111C>G (p.Ser704Cys)
c.2147C>G (p.Ser716Cys)
c.2123C>G (p.Ser708Cys)
13g.108209158G>TCA388614007LIG4c.1910C>A (p.Ser637Tyr)
c.2111C>A (p.Ser704Tyr)
c.2147C>A (p.Ser716Tyr)
c.2123C>A (p.Ser708Tyr)
13g.108209159A=CA2117794066LIG4c.1909T= (p.Ser637=)
c.2110T= (p.Ser704=)
c.2146T= (p.Ser716=)
c.2122T= (p.Ser708=)
13g.108209159A>CCA388614008LIG4c.1909T>G (p.Ser637Ala)
c.2110T>G (p.Ser704Ala)
c.2146T>G (p.Ser716Ala)
c.2122T>G (p.Ser708Ala)
13g.108209159A>GCA7043558LIG4c.1909T>C (p.Ser637Pro)
c.2110T>C (p.Ser704Pro)
c.2146T>C (p.Ser716Pro)
c.2122T>C (p.Ser708Pro)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.108209159A>TCA388614009LIG4c.1909T>A (p.Ser637Thr)
c.2110T>A (p.Ser704Thr)
c.2146T>A (p.Ser716Thr)
c.2122T>A (p.Ser708Thr)
13g.108209160C>ACA484975344LIG4c.1908G>T (p.Gly636=)
c.2109G>T (p.Gly703=)
c.2145G>T (p.Gly715=)
c.2121G>T (p.Gly707=)
13g.108209160C>GCA484975348LIG4c.1908G>C (p.Gly636=)
c.2109G>C (p.Gly703=)
c.2145G>C (p.Gly715=)
c.2121G>C (p.Gly707=)
13g.108209160C>TCA484975349LIG4c.1908G>A (p.Gly636=)
c.2109G>A (p.Gly703=)
c.2145G>A (p.Gly715=)
c.2121G>A (p.Gly707=)
13g.108209161C>ACA388614010LIG4c.1907G>T (p.Gly636Val)
c.2108G>T (p.Gly703Val)
c.2144G>T (p.Gly715Val)
c.2120G>T (p.Gly707Val)
13g.108209161C>GCA388614011LIG4c.1907G>C (p.Gly636Ala)
c.2108G>C (p.Gly703Ala)
c.2144G>C (p.Gly715Ala)
c.2120G>C (p.Gly707Ala)
13g.108209161C>TCA388614012LIG4c.1907G>A (p.Gly636Glu)
c.2108G>A (p.Gly703Glu)
c.2144G>A (p.Gly715Glu)
c.2120G>A (p.Gly707Glu)
13g.108209162C>ACA388614013LIG4c.1906G>T (p.Gly636Trp)
c.2107G>T (p.Gly703Trp)
c.2143G>T (p.Gly715Trp)
c.2119G>T (p.Gly707Trp)
13g.108209162C>GCA388614014LIG4c.1906G>C (p.Gly636Arg)
c.2107G>C (p.Gly703Arg)
c.2143G>C (p.Gly715Arg)
c.2119G>C (p.Gly707Arg)
 gnomAD v4
13g.108209162C>TCA388614015LIG4c.1906G>A (p.Gly636Arg)
c.2107G>A (p.Gly703Arg)
c.2143G>A (p.Gly715Arg)
c.2119G>A (p.Gly707Arg)
13g.108209163T>ACA484975351LIG4c.1905A>T (p.Ala635=)
c.2106A>T (p.Ala702=)
c.2142A>T (p.Ala714=)
c.2118A>T (p.Ala706=)
13g.108209163T>CCA484975353LIG4c.1905A>G (p.Ala635=)
c.2106A>G (p.Ala702=)
c.2142A>G (p.Ala714=)
c.2118A>G (p.Ala706=)
13g.108209163T>GCA484975352LIG4c.1905A>C (p.Ala635=)
c.2106A>C (p.Ala702=)
c.2142A>C (p.Ala714=)
c.2118A>C (p.Ala706=)
13g.108209164G>ACA388614017LIG4c.1904C>T (p.Ala635Val)
c.2105C>T (p.Ala702Val)
c.2141C>T (p.Ala714Val)
c.2117C>T (p.Ala706Val)
 gnomAD v4
13g.108209164G>CCA388614018LIG4c.1904C>G (p.Ala635Gly)
c.2105C>G (p.Ala702Gly)
c.2141C>G (p.Ala714Gly)
c.2117C>G (p.Ala706Gly)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.108209164G=CA2117794067LIG4c.1904C= (p.Ala635=)
c.2105C= (p.Ala702=)
c.2141C= (p.Ala714=)
c.2117C= (p.Ala706=)
13g.108209164G>TCA388614016LIG4c.1904C>A (p.Ala635Glu)
c.2105C>A (p.Ala702Glu)
c.2141C>A (p.Ala714Glu)
c.2117C>A (p.Ala706Glu)
13g.108209165C>ACA388614019LIG4c.1903G>T (p.Ala635Ser)
c.2104G>T (p.Ala702Ser)
c.2140G>T (p.Ala714Ser)
c.2116G>T (p.Ala706Ser)
13g.108209165C>GCA388614021LIG4c.1903G>C (p.Ala635Pro)
c.2104G>C (p.Ala702Pro)
c.2140G>C (p.Ala714Pro)
c.2116G>C (p.Ala706Pro)
13g.108209165C>TCA388614022LIG4c.1903G>A (p.Ala635Thr)
c.2104G>A (p.Ala702Thr)
c.2140G>A (p.Ala714Thr)
c.2116G>A (p.Ala706Thr)
13g.108209166A=CA2117794068LIG4c.1902T= (p.Ile634=)
c.2103T= (p.Ile701=)
c.2139T= (p.Ile713=)
c.2115T= (p.Ile705=)
13g.108209166A>CCA388614024LIG4c.1902T>G (p.Ile634Met)
c.2103T>G (p.Ile701Met)
c.2139T>G (p.Ile713Met)
c.2115T>G (p.Ile705Met)
13g.108209166A>GCA484975361LIG4c.1902T>C (p.Ile634=)
c.2103T>C (p.Ile701=)
c.2139T>C (p.Ile713=)
c.2115T>C (p.Ile705=)
 dbSNP gnomAD v2 gnomAD v4
13g.108209166A>TCA484975362LIG4c.1902T>A (p.Ile634=)
c.2103T>A (p.Ile701=)
c.2139T>A (p.Ile713=)
c.2115T>A (p.Ile705=)
13g.108209167A=CA2117794069LIG4c.1901T= (p.Ile634=)
c.2102T= (p.Ile701=)
c.2138T= (p.Ile713=)
c.2114T= (p.Ile705=)
13g.108209167A>CCA388614030LIG4c.1901T>G (p.Ile634Ser)
c.2102T>G (p.Ile701Ser)
c.2138T>G (p.Ile713Ser)
c.2114T>G (p.Ile705Ser)
13g.108209167A>GCA388614028LIG4c.1901T>C (p.Ile634Thr)
c.2102T>C (p.Ile701Thr)
c.2138T>C (p.Ile713Thr)
c.2114T>C (p.Ile705Thr)
 dbSNP gnomAD v2 gnomAD v4
13g.108209167A>TCA388614026LIG4c.1901T>A (p.Ile634Asn)
c.2102T>A (p.Ile701Asn)
c.2138T>A (p.Ile713Asn)
c.2114T>A (p.Ile705Asn)
13g.108209168T>ACA388614032LIG4c.1900A>T (p.Ile634Phe)
c.2101A>T (p.Ile701Phe)
c.2137A>T (p.Ile713Phe)
c.2113A>T (p.Ile705Phe)
13g.108209168T>CCA388614034LIG4c.1900A>G (p.Ile634Val)
c.2101A>G (p.Ile701Val)
c.2137A>G (p.Ile713Val)
c.2113A>G (p.Ile705Val)
 gnomAD v4
13g.108209168T>GCA388614036LIG4c.1900A>C (p.Ile634Leu)
c.2101A>C (p.Ile701Leu)
c.2137A>C (p.Ile713Leu)
c.2113A>C (p.Ile705Leu)
 dbSNP
13g.108209168T=CA2117794070LIG4c.1900A= (p.Ile634=)
c.2101A= (p.Ile701=)
c.2137A= (p.Ile713=)
c.2113A= (p.Ile705=)
13g.108209168_108209175delinsTTACACAGCA2117794071LIG4c.1893_1900delinsCTGTGTAA (p.Tyr631=)
c.2094_2101delinsCTGTGTAA (p.Tyr698=)
c.2130_2137delinsCTGTGTAA (p.Tyr710=)
c.2106_2113delinsCTGTGTAA (p.Tyr702=)
13g.108209169T>ACA484975363LIG4c.1899A>T (p.Val633=)
c.2100A>T (p.Val700=)
c.2136A>T (p.Val712=)
c.2112A>T (p.Val704=)
13g.108209169T>CCA484975366LIG4c.1899A>G (p.Val633=)
c.2100A>G (p.Val700=)
c.2136A>G (p.Val712=)
c.2112A>G (p.Val704=)
13g.108209169T>GCA484975368LIG4c.1899A>C (p.Val633=)
c.2100A>C (p.Val700=)
c.2136A>C (p.Val712=)
c.2112A>C (p.Val704=)
13g.108209172_108209178delCA694834317LIG4c.1893_1899del (p.Tyr631Ter)
c.2094_2100del (p.Tyr698Ter)
c.2130_2136del (p.Tyr710Ter)
c.2106_2112del (p.Tyr702Ter)
 dbSNP gnomAD v3 gnomAD v4
13g.108209170A>CCA388614038LIG4c.1898T>G (p.Val633Gly)
c.2099T>G (p.Val700Gly)
c.2135T>G (p.Val712Gly)
c.2111T>G (p.Val704Gly)
13g.108209170A>GCA388614040LIG4c.1898T>C (p.Val633Ala)
c.2099T>C (p.Val700Ala)
c.2135T>C (p.Val712Ala)
c.2111T>C (p.Val704Ala)
13g.108209170A>TCA388614042LIG4c.1898T>A (p.Val633Glu)
c.2099T>A (p.Val700Glu)
c.2135T>A (p.Val712Glu)
c.2111T>A (p.Val704Glu)
13g.108209170dupCA2623644101LIG4c.1898dup (p.Ile634AsnfsTer5)
c.2099dup (p.Ile701AsnfsTer5)
c.2135dup (p.Ile713AsnfsTer5)
c.2111dup (p.Ile705AsnfsTer5)
 gnomAD v4
13g.108209171C>ACA388614045LIG4c.1897G>T (p.Val633Leu)
c.2098G>T (p.Val700Leu)
c.2134G>T (p.Val712Leu)
c.2110G>T (p.Val704Leu)
13g.108209171C=CA2117794072LIG4c.1897G= (p.Val633=)
c.2098G= (p.Val700=)
c.2134G= (p.Val712=)
c.2110G= (p.Val704=)
13g.108209171C>GCA388614048LIG4c.1897G>C (p.Val633Leu)
c.2098G>C (p.Val700Leu)
c.2134G>C (p.Val712Leu)
c.2110G>C (p.Val704Leu)
13g.108209171C>TCA388614047LIG4c.1897G>A (p.Val633Ile)
c.2098G>A (p.Val700Ile)
c.2134G>A (p.Val712Ile)
c.2110G>A (p.Val704Ile)
 dbSNP gnomAD v3 gnomAD v4
13g.108209172A>CCA388614050LIG4c.1896T>G (p.Cys632Trp)
c.2097T>G (p.Cys699Trp)
c.2133T>G (p.Cys711Trp)
c.2109T>G (p.Cys703Trp)
13g.108209172A>GCA484975373LIG4c.1896T>C (p.Cys632=)
c.2097T>C (p.Cys699=)
c.2133T>C (p.Cys711=)
c.2109T>C (p.Cys703=)
13g.108209172A>TCA388614052LIG4c.1896T>A (p.Cys632Ter)
c.2097T>A (p.Cys699Ter)
c.2133T>A (p.Cys711Ter)
c.2109T>A (p.Cys703Ter)
13g.108209173C>ACA256180034LIG4c.1895G>T (p.Cys632Phe)
c.2096G>T (p.Cys699Phe)
c.2132G>T (p.Cys711Phe)
c.2108G>T (p.Cys703Phe)
 dbSNP
13g.108209173C=CA2117794073LIG4c.1895G= (p.Cys632=)
c.2096G= (p.Cys699=)
c.2132G= (p.Cys711=)
c.2108G= (p.Cys703=)
13g.108209173C>GCA388614054LIG4c.1895G>C (p.Cys632Ser)
c.2096G>C (p.Cys699Ser)
c.2132G>C (p.Cys711Ser)
c.2108G>C (p.Cys703Ser)
13g.108209173C>TCA388614055LIG4c.1895G>A (p.Cys632Tyr)
c.2096G>A (p.Cys699Tyr)
c.2132G>A (p.Cys711Tyr)
c.2108G>A (p.Cys703Tyr)
13g.108209174A=CA2117794074LIG4c.1894T= (p.Cys632=)
c.2095T= (p.Cys699=)
c.2131T= (p.Cys711=)
c.2107T= (p.Cys703=)
13g.108209174A>CCA388614056LIG4c.1894T>G (p.Cys632Gly)
c.2095T>G (p.Cys699Gly)
c.2131T>G (p.Cys711Gly)
c.2107T>G (p.Cys703Gly)
13g.108209174A>GCA388614058LIG4c.1894T>C (p.Cys632Arg)
c.2095T>C (p.Cys699Arg)
c.2131T>C (p.Cys711Arg)
c.2107T>C (p.Cys703Arg)
 dbSNP
13g.108209174A>TCA388614059LIG4c.1894T>A (p.Cys632Ser)
c.2095T>A (p.Cys699Ser)
c.2131T>A (p.Cys711Ser)
c.2107T>A (p.Cys703Ser)
13g.108209175G>ACA484975382LIG4c.1893C>T (p.Tyr631=)
c.2094C>T (p.Tyr698=)
c.2130C>T (p.Tyr710=)
c.2106C>T (p.Tyr702=)
13g.108209175G>CCA7043559LIG4c.1893C>G (p.Tyr631Ter)
c.2094C>G (p.Tyr698Ter)
c.2130C>G (p.Tyr710Ter)
c.2106C>G (p.Tyr702Ter)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.108209175G=CA2117794075LIG4c.1893C= (p.Tyr631=)
c.2094C= (p.Tyr698=)
c.2130C= (p.Tyr710=)
c.2106C= (p.Tyr702=)
13g.108209175G>TCA388614063LIG4c.1893C>A (p.Tyr631Ter)
c.2094C>A (p.Tyr698Ter)
c.2130C>A (p.Tyr710Ter)
c.2106C>A (p.Tyr702Ter)
13g.108209176T>ACA388614064LIG4c.1892A>T (p.Tyr631Phe)
c.2093A>T (p.Tyr698Phe)
c.2129A>T (p.Tyr710Phe)
c.2105A>T (p.Tyr702Phe)
13g.108209176T>CCA388614066LIG4c.1892A>G (p.Tyr631Cys)
c.2093A>G (p.Tyr698Cys)
c.2129A>G (p.Tyr710Cys)
c.2105A>G (p.Tyr702Cys)
 gnomAD v4
13g.108209176T>GCA388614067LIG4c.1892A>C (p.Tyr631Ser)
c.2093A>C (p.Tyr698Ser)
c.2129A>C (p.Tyr710Ser)
c.2105A>C (p.Tyr702Ser)
13g.108209177A>CCA388614071LIG4c.1891T>G (p.Tyr631Asp)
c.2092T>G (p.Tyr698Asp)
c.2128T>G (p.Tyr710Asp)
c.2104T>G (p.Tyr702Asp)
 gnomAD v4
13g.108209177A>GCA388614069LIG4c.1891T>C (p.Tyr631His)
c.2092T>C (p.Tyr698His)
c.2128T>C (p.Tyr710His)
c.2104T>C (p.Tyr702His)
13g.108209177A>TCA388614068LIG4c.1891T>A (p.Tyr631Asn)
c.2092T>A (p.Tyr698Asn)
c.2128T>A (p.Tyr710Asn)
c.2104T>A (p.Tyr702Asn)
13g.108209178C>ACA484975391LIG4c.1890G>T (p.Thr630=)
c.2091G>T (p.Thr697=)
c.2127G>T (p.Thr709=)
c.2103G>T (p.Thr701=)
 gnomAD v4
13g.108209178C=CA2117794076LIG4c.1890G= (p.Thr630=)
c.2091G= (p.Thr697=)
c.2127G= (p.Thr709=)
c.2103G= (p.Thr701=)
13g.108209178C>GCA484975393LIG4c.1890G>C (p.Thr630=)
c.2091G>C (p.Thr697=)
c.2127G>C (p.Thr709=)
c.2103G>C (p.Thr701=)
 gnomAD v4
13g.108209178C>TCA7043560LIG4c.1890G>A (p.Thr630=)
c.2091G>A (p.Thr697=)
c.2127G>A (p.Thr709=)
c.2103G>A (p.Thr701=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
13g.108209179G>ACA388614074LIG4c.1889C>T (p.Thr630Met)
c.2090C>T (p.Thr697Met)
c.2126C>T (p.Thr709Met)
c.2102C>T (p.Thr701Met)
 gnomAD v4 COSMIC
13g.108209179G>CCA388614075LIG4c.1889C>G (p.Thr630Arg)
c.2090C>G (p.Thr697Arg)
c.2126C>G (p.Thr709Arg)
c.2102C>G (p.Thr701Arg)
13g.108209179G>TCA388614077LIG4c.1889C>A (p.Thr630Lys)
c.2090C>A (p.Thr697Lys)
c.2126C>A (p.Thr709Lys)
c.2102C>A (p.Thr701Lys)
13g.108209180T>ACA388614078LIG4c.1888A>T (p.Thr630Ser)
c.2089A>T (p.Thr697Ser)
c.2125A>T (p.Thr709Ser)
c.2101A>T (p.Thr701Ser)
13g.108209180T>CCA388614080LIG4c.1888A>G (p.Thr630Ala)
c.2089A>G (p.Thr697Ala)
c.2125A>G (p.Thr709Ala)
c.2101A>G (p.Thr701Ala)
13g.108209180T>GCA388614081LIG4c.1888A>C (p.Thr630Pro)
c.2089A>C (p.Thr697Pro)
c.2125A>C (p.Thr709Pro)
c.2101A>C (p.Thr701Pro)
13g.108209181G>ACA484975398LIG4c.1887C>T (p.Asp629=)
c.2088C>T (p.Asp696=)
c.2124C>T (p.Asp708=)
c.2100C>T (p.Asp700=)
13g.108209181G>CCA388614084LIG4c.1887C>G (p.Asp629Glu)
c.2088C>G (p.Asp696Glu)
c.2124C>G (p.Asp708Glu)
c.2100C>G (p.Asp700Glu)
13g.108209181G>TCA388614085LIG4c.1887C>A (p.Asp629Glu)
c.2088C>A (p.Asp696Glu)
c.2124C>A (p.Asp708Glu)
c.2100C>A (p.Asp700Glu)
13g.108209182T>ACA388614087LIG4c.1886A>T (p.Asp629Val)
c.2087A>T (p.Asp696Val)
c.2123A>T (p.Asp708Val)
c.2099A>T (p.Asp700Val)
13g.108209182T>CCA7043561LIG4c.1886A>G (p.Asp629Gly)
c.2087A>G (p.Asp696Gly)
c.2123A>G (p.Asp708Gly)
c.2099A>G (p.Asp700Gly)
 dbSNP ExAC gnomAD v2
13g.108209182T>GCA388614090LIG4c.1886A>C (p.Asp629Ala)
c.2087A>C (p.Asp696Ala)
c.2123A>C (p.Asp708Ala)
c.2099A>C (p.Asp700Ala)
13g.108209182T=CA2117794077LIG4c.1886A= (p.Asp629=)
c.2087A= (p.Asp696=)
c.2123A= (p.Asp708=)
c.2099A= (p.Asp700=)
13g.108209183C>ACA388614095LIG4c.1885G>T (p.Asp629Tyr)
c.2086G>T (p.Asp696Tyr)
c.2122G>T (p.Asp708Tyr)
c.2098G>T (p.Asp700Tyr)
13g.108209183C>GCA388614097LIG4c.1885G>C (p.Asp629His)
c.2086G>C (p.Asp696His)
c.2122G>C (p.Asp708His)
c.2098G>C (p.Asp700His)
 COSMIC
13g.108209183C>TCA388614093LIG4c.1885G>A (p.Asp629Asn)
c.2086G>A (p.Asp696Asn)
c.2122G>A (p.Asp708Asn)
c.2098G>A (p.Asp700Asn)
13g.108209184T>ACA484975404LIG4c.1884A>T (p.Pro628=)
c.2085A>T (p.Pro695=)
c.2121A>T (p.Pro707=)
c.2097A>T (p.Pro699=)
13g.108209184T>CCA484975405LIG4c.1884A>G (p.Pro628=)
c.2085A>G (p.Pro695=)
c.2121A>G (p.Pro707=)
c.2097A>G (p.Pro699=)
13g.108209184T>GCA484975406LIG4c.1884A>C (p.Pro628=)
c.2085A>C (p.Pro695=)
c.2121A>C (p.Pro707=)
c.2097A>C (p.Pro699=)
13g.108209184_108209185delinsTGCA2117794078LIG4c.1883_1884delinsCA (p.Pro628=)
c.2084_2085delinsCA (p.Pro695=)
c.2120_2121delinsCA (p.Pro707=)
c.2096_2097delinsCA (p.Pro699=)
13g.108209185G>ACA388614098LIG4c.1883C>T (p.Pro628Leu)
c.2084C>T (p.Pro695Leu)
c.2120C>T (p.Pro707Leu)
c.2096C>T (p.Pro699Leu)
13g.108209185G>CCA388614099LIG4c.1883C>G (p.Pro628Arg)
c.2084C>G (p.Pro695Arg)
c.2120C>G (p.Pro707Arg)
c.2096C>G (p.Pro699Arg)
13g.108209185G>TCA388614100LIG4c.1883C>A (p.Pro628Gln)
c.2084C>A (p.Pro695Gln)
c.2120C>A (p.Pro707Gln)
c.2096C>A (p.Pro699Gln)
13g.108209187delCA612360450LIG4c.1883del (p.Pro628GlnfsTer6)
c.2084del (p.Pro695GlnfsTer6)
c.2120del (p.Pro707GlnfsTer6)
c.2096del (p.Pro699GlnfsTer6)
 dbSNP gnomAD v2 gnomAD v4
13g.108209186G>ACA388614101LIG4c.1882C>T (p.Pro628Ser)
c.2083C>T (p.Pro695Ser)
c.2119C>T (p.Pro707Ser)
c.2095C>T (p.Pro699Ser)
13g.108209186G>CCA388614102LIG4c.1882C>G (p.Pro628Ala)
c.2083C>G (p.Pro695Ala)
c.2119C>G (p.Pro707Ala)
c.2095C>G (p.Pro699Ala)
13g.108209186G>TCA388614103LIG4c.1882C>A (p.Pro628Thr)
c.2083C>A (p.Pro695Thr)
c.2119C>A (p.Pro707Thr)
c.2095C>A (p.Pro699Thr)
13g.108209187G>ACA484975411LIG4c.1881C>T (p.Gly627=)
c.2082C>T (p.Gly694=)
c.2118C>T (p.Gly706=)
c.2094C>T (p.Gly698=)
 dbSNP gnomAD v2 gnomAD v4
13g.108209187G>CCA484975412LIG4c.1881C>G (p.Gly627=)
c.2082C>G (p.Gly694=)
c.2118C>G (p.Gly706=)
c.2094C>G (p.Gly698=)
13g.108209187G=CA2117794079LIG4c.1881C= (p.Gly627=)
c.2082C= (p.Gly694=)
c.2118C= (p.Gly706=)
c.2094C= (p.Gly698=)
13g.108209187G>TCA484975413LIG4c.1881C>A (p.Gly627=)
c.2082C>A (p.Gly694=)
c.2118C>A (p.Gly706=)
c.2094C>A (p.Gly698=)
13g.108209188C>ACA388614104LIG4c.1880G>T (p.Gly627Val)
c.2081G>T (p.Gly694Val)
c.2117G>T (p.Gly706Val)
c.2093G>T (p.Gly698Val)
13g.108209188C>GCA388614106LIG4c.1880G>C (p.Gly627Ala)
c.2081G>C (p.Gly694Ala)
c.2117G>C (p.Gly706Ala)
c.2093G>C (p.Gly698Ala)
13g.108209188C>TCA388614107LIG4c.1880G>A (p.Gly627Asp)
c.2081G>A (p.Gly694Asp)
c.2117G>A (p.Gly706Asp)
c.2093G>A (p.Gly698Asp)
13g.108209189C>ACA388614109LIG4c.1879G>T (p.Gly627Cys)
c.2080G>T (p.Gly694Cys)
c.2116G>T (p.Gly706Cys)
c.2092G>T (p.Gly698Cys)
13g.108209189C>GCA388614110LIG4c.1879G>C (p.Gly627Arg)
c.2080G>C (p.Gly694Arg)
c.2116G>C (p.Gly706Arg)
c.2092G>C (p.Gly698Arg)
13g.108209189C>TCA388614112LIG4c.1879G>A (p.Gly627Ser)
c.2080G>A (p.Gly694Ser)
c.2116G>A (p.Gly706Ser)
c.2092G>A (p.Gly698Ser)
13g.108209190T>ACA484975420LIG4c.1878A>T (p.Pro626=)
c.2079A>T (p.Pro693=)
c.2115A>T (p.Pro705=)
c.2091A>T (p.Pro697=)
13g.108209190T>CCA484975423LIG4c.1878A>G (p.Pro626=)
c.2079A>G (p.Pro693=)
c.2115A>G (p.Pro705=)
c.2091A>G (p.Pro697=)
13g.108209190T>GCA484975424LIG4c.1878A>C (p.Pro626=)
c.2079A>C (p.Pro693=)
c.2115A>C (p.Pro705=)
c.2091A>C (p.Pro697=)
13g.108209191G>ACA256180099LIG4c.1877C>T (p.Pro626Leu)
c.2078C>T (p.Pro693Leu)
c.2114C>T (p.Pro705Leu)
c.2090C>T (p.Pro697Leu)
 dbSNP
13g.108209191G>CCA388614116LIG4c.1877C>G (p.Pro626Arg)
c.2078C>G (p.Pro693Arg)
c.2114C>G (p.Pro705Arg)
c.2090C>G (p.Pro697Arg)
13g.108209191G=CA2117794080LIG4c.1877C= (p.Pro626=)
c.2078C= (p.Pro693=)
c.2114C= (p.Pro705=)
c.2090C= (p.Pro697=)
13g.108209191G>TCA388614114LIG4c.1877C>A (p.Pro626Gln)
c.2078C>A (p.Pro693Gln)
c.2114C>A (p.Pro705Gln)
c.2090C>A (p.Pro697Gln)
13g.108209192G>ACA388614118LIG4c.1876C>T (p.Pro626Ser)
c.2077C>T (p.Pro693Ser)
c.2113C>T (p.Pro705Ser)
c.2089C>T (p.Pro697Ser)
 dbSNP gnomAD v2 gnomAD v4
13g.108209192G>CCA388614119LIG4c.1876C>G (p.Pro626Ala)
c.2077C>G (p.Pro693Ala)
c.2113C>G (p.Pro705Ala)
c.2089C>G (p.Pro697Ala)
 gnomAD v4
13g.108209192G=CA2117794081LIG4c.1876C= (p.Pro626=)
c.2077C= (p.Pro693=)
c.2113C= (p.Pro705=)
c.2089C= (p.Pro697=)
13g.108209192G>TCA388614120LIG4c.1876C>A (p.Pro626Thr)
c.2077C>A (p.Pro693Thr)
c.2113C>A (p.Pro705Thr)
c.2089C>A (p.Pro697Thr)
13g.108209193A>CCA388614121LIG4c.1875T>G (p.Asn625Lys)
c.2076T>G (p.Asn692Lys)
c.2112T>G (p.Asn704Lys)
c.2088T>G (p.Asn696Lys)
13g.108209193A>GCA484975428LIG4c.1875T>C (p.Asn625=)
c.2076T>C (p.Asn692=)
c.2112T>C (p.Asn704=)
c.2088T>C (p.Asn696=)
13g.108209193A>TCA388614122LIG4c.1875T>A (p.Asn625Lys)
c.2076T>A (p.Asn692Lys)
c.2112T>A (p.Asn704Lys)
c.2088T>A (p.Asn696Lys)
13g.108209194T>ACA388614125LIG4c.1874A>T (p.Asn625Ile)
c.2075A>T (p.Asn692Ile)
c.2111A>T (p.Asn704Ile)
c.2087A>T (p.Asn696Ile)
13g.108209194T>CCA388614123LIG4c.1874A>G (p.Asn625Ser)
c.2075A>G (p.Asn692Ser)
c.2111A>G (p.Asn704Ser)
c.2087A>G (p.Asn696Ser)
13g.108209194T>GCA388614124LIG4c.1874A>C (p.Asn625Thr)
c.2075A>C (p.Asn692Thr)
c.2111A>C (p.Asn704Thr)
c.2087A>C (p.Asn696Thr)
13g.108209195T>ACA388614128LIG4c.1873A>T (p.Asn625Tyr)
c.2074A>T (p.Asn692Tyr)
c.2110A>T (p.Asn704Tyr)
c.2086A>T (p.Asn696Tyr)
13g.108209195T>CCA388614130LIG4c.1873A>G (p.Asn625Asp)
c.2074A>G (p.Asn692Asp)
c.2110A>G (p.Asn704Asp)
c.2086A>G (p.Asn696Asp)
13g.108209195T>GCA388614132LIG4c.1873A>C (p.Asn625His)
c.2074A>C (p.Asn692His)
c.2110A>C (p.Asn704His)
c.2086A>C (p.Asn696His)
13g.108209196T>ACA388614136LIG4c.1872A>T (p.Gln624His)
c.2073A>T (p.Gln691His)
c.2109A>T (p.Gln703His)
c.2085A>T (p.Gln695His)
13g.108209196T>CCA484975432LIG4c.1872A>G (p.Gln624=)
c.2073A>G (p.Gln691=)
c.2109A>G (p.Gln703=)
c.2085A>G (p.Gln695=)
13g.108209196T>GCA388614139LIG4c.1872A>C (p.Gln624His)
c.2073A>C (p.Gln691His)
c.2109A>C (p.Gln703His)
c.2085A>C (p.Gln695His)
13g.108209197T>ACA388614144LIG4c.1871A>T (p.Gln624Leu)
c.2072A>T (p.Gln691Leu)
c.2108A>T (p.Gln703Leu)
c.2084A>T (p.Gln695Leu)
13g.108209197T>CCA256180106LIG4c.1871A>G (p.Gln624Arg)
c.2072A>G (p.Gln691Arg)
c.2108A>G (p.Gln703Arg)
c.2084A>G (p.Gln695Arg)
 dbSNP
13g.108209197T>GCA388614142LIG4c.1871A>C (p.Gln624Pro)
c.2072A>C (p.Gln691Pro)
c.2108A>C (p.Gln703Pro)
c.2084A>C (p.Gln695Pro)
13g.108209197T=CA2117794082LIG4c.1871A= (p.Gln624=)
c.2072A= (p.Gln691=)
c.2108A= (p.Gln703=)
c.2084A= (p.Gln695=)
13g.108209198G>ACA388614145LIG4c.1870C>T (p.Gln624Ter)
c.2071C>T (p.Gln691Ter)
c.2107C>T (p.Gln703Ter)
c.2083C>T (p.Gln695Ter)
13g.108209198G>CCA388614149LIG4c.1870C>G (p.Gln624Glu)
c.2071C>G (p.Gln691Glu)
c.2107C>G (p.Gln703Glu)
c.2083C>G (p.Gln695Glu)
13g.108209198G>TCA388614147LIG4c.1870C>A (p.Gln624Lys)
c.2071C>A (p.Gln691Lys)
c.2107C>A (p.Gln703Lys)
c.2083C>A (p.Gln695Lys)
13g.108209199T>ACA484975437LIG4c.1869A>T (p.Val623=)
c.2070A>T (p.Val690=)
c.2106A>T (p.Val702=)
c.2082A>T (p.Val694=)
13g.108209199T>CCA484975438LIG4c.1869A>G (p.Val623=)
c.2070A>G (p.Val690=)
c.2106A>G (p.Val702=)
c.2082A>G (p.Val694=)
13g.108209199T>GCA484975439LIG4c.1869A>C (p.Val623=)
c.2070A>C (p.Val690=)
c.2106A>C (p.Val702=)
c.2082A>C (p.Val694=)
13g.108209200A>CCA388614150LIG4c.1868T>G (p.Val623Gly)
c.2069T>G (p.Val690Gly)
c.2105T>G (p.Val702Gly)
c.2081T>G (p.Val694Gly)
13g.108209200A>GCA388614154LIG4c.1868T>C (p.Val623Ala)
c.2069T>C (p.Val690Ala)
c.2105T>C (p.Val702Ala)
c.2081T>C (p.Val694Ala)
13g.108209200A>TCA388614152LIG4c.1868T>A (p.Val623Glu)
c.2069T>A (p.Val690Glu)
c.2105T>A (p.Val702Glu)
c.2081T>A (p.Val694Glu)
13g.108209201C>ACA388614155LIG4c.1867G>T (p.Val623Leu)
c.2068G>T (p.Val690Leu)
c.2104G>T (p.Val702Leu)
c.2080G>T (p.Val694Leu)
 gnomAD v4
13g.108209201C=CA2117794083LIG4c.1867G= (p.Val623=)
c.2068G= (p.Val690=)
c.2104G= (p.Val702=)
c.2080G= (p.Val694=)
13g.108209201C>GCA388614159LIG4c.1867G>C (p.Val623Leu)
c.2068G>C (p.Val690Leu)
c.2104G>C (p.Val702Leu)
c.2080G>C (p.Val694Leu)
13g.108209201C>TCA388614157LIG4c.1867G>A (p.Val623Ile)
c.2068G>A (p.Val690Ile)
c.2104G>A (p.Val702Ile)
c.2080G>A (p.Val694Ile)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.108209202T>ACA484975441LIG4c.1866A>T (p.Ile622=)
c.2067A>T (p.Ile689=)
c.2103A>T (p.Ile701=)
c.2079A>T (p.Ile693=)
 ClinVar
13g.108209202T>CCA256180112LIG4c.1866A>G (p.Ile622Met)
c.2067A>G (p.Ile689Met)
c.2103A>G (p.Ile701Met)
c.2079A>G (p.Ile693Met)
 dbSNP
13g.108209202T>GCA484975443LIG4c.1866A>C (p.Ile622=)
c.2067A>C (p.Ile689=)
c.2103A>C (p.Ile701=)
c.2079A>C (p.Ile693=)
13g.108209202T=CA2117794084LIG4c.1866A= (p.Ile622=)
c.2067A= (p.Ile689=)
c.2103A= (p.Ile701=)
c.2079A= (p.Ile693=)
13g.108209203A=CA2117794085LIG4c.1865T= (p.Ile622=)
c.2066T= (p.Ile689=)
c.2102T= (p.Ile701=)
c.2078T= (p.Ile693=)
13g.108209203A>CCA388614161LIG4c.1865T>G (p.Ile622Arg)
c.2066T>G (p.Ile689Arg)
c.2102T>G (p.Ile701Arg)
c.2078T>G (p.Ile693Arg)
13g.108209203A>GCA7043562LIG4c.1865T>C (p.Ile622Thr)
c.2066T>C (p.Ile689Thr)
c.2102T>C (p.Ile701Thr)
c.2078T>C (p.Ile693Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.108209203A>TCA388614164LIG4c.1865T>A (p.Ile622Lys)
c.2066T>A (p.Ile689Lys)
c.2102T>A (p.Ile701Lys)
c.2078T>A (p.Ile693Lys)
13g.108209204T>ACA388614167LIG4c.1864A>T (p.Ile622Leu)
c.2065A>T (p.Ile689Leu)
c.2101A>T (p.Ile701Leu)
c.2077A>T (p.Ile693Leu)
13g.108209204T>CCA388614171LIG4c.1864A>G (p.Ile622Val)
c.2065A>G (p.Ile689Val)
c.2101A>G (p.Ile701Val)
c.2077A>G (p.Ile693Val)
 dbSNP gnomAD v4
13g.108209204T>GCA388614174LIG4c.1864A>C (p.Ile622Leu)
c.2065A>C (p.Ile689Leu)
c.2101A>C (p.Ile701Leu)
c.2077A>C (p.Ile693Leu)
13g.108209204T=CA2117794086LIG4c.1864A= (p.Ile622=)
c.2065A= (p.Ile689=)
c.2101A= (p.Ile701=)
c.2077A= (p.Ile693=)
13g.108209205A=CA2117794087LIG4c.1863T= (p.Tyr621=)
c.2064T= (p.Tyr688=)
c.2100T= (p.Tyr700=)
c.2076T= (p.Tyr692=)
13g.108209205A>CCA388614176LIG4c.1863T>G (p.Tyr621Ter)
c.2064T>G (p.Tyr688Ter)
c.2100T>G (p.Tyr700Ter)
c.2076T>G (p.Tyr692Ter)
13g.108209205A>GCA484975452LIG4c.1863T>C (p.Tyr621=)
c.2064T>C (p.Tyr688=)
c.2100T>C (p.Tyr700=)
c.2076T>C (p.Tyr692=)
 dbSNP
13g.108209205A>TCA388614179LIG4c.1863T>A (p.Tyr621Ter)
c.2064T>A (p.Tyr688Ter)
c.2100T>A (p.Tyr700Ter)
c.2076T>A (p.Tyr692Ter)
13g.108209206T>ACA388614183LIG4c.1862A>T (p.Tyr621Phe)
c.2063A>T (p.Tyr688Phe)
c.2099A>T (p.Tyr700Phe)
c.2075A>T (p.Tyr692Phe)
13g.108209206T>CCA388614185LIG4c.1862A>G (p.Tyr621Cys)
c.2063A>G (p.Tyr688Cys)
c.2099A>G (p.Tyr700Cys)
c.2075A>G (p.Tyr692Cys)
 gnomAD v4
13g.108209206T>GCA388614186LIG4c.1862A>C (p.Tyr621Ser)
c.2063A>C (p.Tyr688Ser)
c.2099A>C (p.Tyr700Ser)
c.2075A>C (p.Tyr692Ser)
13g.108209207A=CA2117794088LIG4c.1861T= (p.Tyr621=)
c.2062T= (p.Tyr688=)
c.2098T= (p.Tyr700=)
c.2074T= (p.Tyr692=)
13g.108209207A>CCA388614189LIG4c.1861T>G (p.Tyr621Asp)
c.2062T>G (p.Tyr688Asp)
c.2098T>G (p.Tyr700Asp)
c.2074T>G (p.Tyr692Asp)
13g.108209207A>GCA388614194LIG4c.1861T>C (p.Tyr621His)
c.2062T>C (p.Tyr688His)
c.2098T>C (p.Tyr700His)
c.2074T>C (p.Tyr692His)
 dbSNP gnomAD v3 gnomAD v4
13g.108209207A>TCA388614192LIG4c.1861T>A (p.Tyr621Asn)
c.2062T>A (p.Tyr688Asn)
c.2098T>A (p.Tyr700Asn)
c.2074T>A (p.Tyr692Asn)
13g.108209208A>CCA484975458LIG4c.1860T>G (p.Gly620=)
c.2061T>G (p.Gly687=)
c.2097T>G (p.Gly699=)
c.2073T>G (p.Gly691=)
 COSMIC
13g.108209208A>GCA484975459LIG4c.1860T>C (p.Gly620=)
c.2061T>C (p.Gly687=)
c.2097T>C (p.Gly699=)
c.2073T>C (p.Gly691=)
13g.108209208A>TCA484975461LIG4c.1860T>A (p.Gly620=)
c.2061T>A (p.Gly687=)
c.2097T>A (p.Gly699=)
c.2073T>A (p.Gly691=)
13g.108209209C>ACA388614196LIG4c.1859G>T (p.Gly620Val)
c.2060G>T (p.Gly687Val)
c.2096G>T (p.Gly699Val)
c.2072G>T (p.Gly691Val)
 gnomAD v4
13g.108209209C=CA2117794089LIG4c.1859G= (p.Gly620=)
c.2060G= (p.Gly687=)
c.2096G= (p.Gly699=)
c.2072G= (p.Gly691=)
13g.108209209C>GCA388614198LIG4c.1859G>C (p.Gly620Ala)
c.2060G>C (p.Gly687Ala)
c.2096G>C (p.Gly699Ala)
c.2072G>C (p.Gly691Ala)
 dbSNP
13g.108209209C>TCA388614201LIG4c.1859G>A (p.Gly620Asp)
c.2060G>A (p.Gly687Asp)
c.2096G>A (p.Gly699Asp)
c.2072G>A (p.Gly691Asp)
13g.108209210C>ACA388614205LIG4c.1858G>T (p.Gly620Cys)
c.2059G>T (p.Gly687Cys)
c.2095G>T (p.Gly699Cys)
c.2071G>T (p.Gly691Cys)
 dbSNP COSMIC
13g.108209210C=CA2117794090LIG4c.1858G= (p.Gly620=)
c.2059G= (p.Gly687=)
c.2095G= (p.Gly699=)
c.2071G= (p.Gly691=)
13g.108209210C>GCA388614208LIG4c.1858G>C (p.Gly620Arg)
c.2059G>C (p.Gly687Arg)
c.2095G>C (p.Gly699Arg)
c.2071G>C (p.Gly691Arg)
13g.108209210C>TCA388614210LIG4c.1858G>A (p.Gly620Ser)
c.2059G>A (p.Gly687Ser)
c.2095G>A (p.Gly699Ser)
c.2071G>A (p.Gly691Ser)
 ClinVar gnomAD v4
13g.108209211A>CCA484975462LIG4c.1857T>G (p.Gly619=)
c.2058T>G (p.Gly686=)
c.2094T>G (p.Gly698=)
c.2070T>G (p.Gly690=)
13g.108209211A>GCA484975463LIG4c.1857T>C (p.Gly619=)
c.2058T>C (p.Gly686=)
c.2094T>C (p.Gly698=)
c.2070T>C (p.Gly690=)
13g.108209211A>TCA484975464LIG4c.1857T>A (p.Gly619=)
c.2058T>A (p.Gly686=)
c.2094T>A (p.Gly698=)
c.2070T>A (p.Gly690=)
13g.108209212C>ACA388614211LIG4c.1856G>T (p.Gly619Val)
c.2057G>T (p.Gly686Val)
c.2093G>T (p.Gly698Val)
c.2069G>T (p.Gly690Val)
13g.108209212C>GCA388614213LIG4c.1856G>C (p.Gly619Ala)
c.2057G>C (p.Gly686Ala)
c.2093G>C (p.Gly698Ala)
c.2069G>C (p.Gly690Ala)
13g.108209212C>TCA388614216LIG4c.1856G>A (p.Gly619Asp)
c.2057G>A (p.Gly686Asp)
c.2093G>A (p.Gly698Asp)
c.2069G>A (p.Gly690Asp)
13g.108209213C>ACA388614218LIG4c.1855G>T (p.Gly619Cys)
c.2056G>T (p.Gly686Cys)
c.2092G>T (p.Gly698Cys)
c.2068G>T (p.Gly690Cys)
13g.108209213C=CA2117794091LIG4c.1855G= (p.Gly619=)
c.2056G= (p.Gly686=)
c.2092G= (p.Gly698=)
c.2068G= (p.Gly690=)
13g.108209213C>GCA388614219LIG4c.1855G>C (p.Gly619Arg)
c.2056G>C (p.Gly686Arg)
c.2092G>C (p.Gly698Arg)
c.2068G>C (p.Gly690Arg)
13g.108209213C>TCA388614217LIG4c.1855G>A (p.Gly619Ser)
c.2056G>A (p.Gly686Ser)
c.2092G>A (p.Gly698Ser)
c.2068G>A (p.Gly690Ser)
 dbSNP gnomAD v2 gnomAD v4
13g.108209214A>CCA388614222LIG4c.1854T>G (p.Phe618Leu)
c.2055T>G (p.Phe685Leu)
c.2091T>G (p.Phe697Leu)
c.2067T>G (p.Phe689Leu)
13g.108209214A>GCA484975472LIG4c.1854T>C (p.Phe618=)
c.2055T>C (p.Phe685=)
c.2091T>C (p.Phe697=)
c.2067T>C (p.Phe689=)
13g.108209214A>TCA388614225LIG4c.1854T>A (p.Phe618Leu)
c.2055T>A (p.Phe685Leu)
c.2091T>A (p.Phe697Leu)
c.2067T>A (p.Phe689Leu)
13g.108209215A>CCA388614227LIG4c.1853T>G (p.Phe618Cys)
c.2054T>G (p.Phe685Cys)
c.2090T>G (p.Phe697Cys)
c.2066T>G (p.Phe689Cys)
13g.108209215A>GCA388614228LIG4c.1853T>C (p.Phe618Ser)
c.2054T>C (p.Phe685Ser)
c.2090T>C (p.Phe697Ser)
c.2066T>C (p.Phe689Ser)
13g.108209215A>TCA388614230LIG4c.1853T>A (p.Phe618Tyr)
c.2054T>A (p.Phe685Tyr)
c.2090T>A (p.Phe697Tyr)
c.2066T>A (p.Phe689Tyr)
13g.108209216A>CCA388614232LIG4c.1852T>G (p.Phe618Val)
c.2053T>G (p.Phe685Val)
c.2089T>G (p.Phe697Val)
c.2065T>G (p.Phe689Val)
13g.108209216A>GCA388614235LIG4c.1852T>C (p.Phe618Leu)
c.2053T>C (p.Phe685Leu)
c.2089T>C (p.Phe697Leu)
c.2065T>C (p.Phe689Leu)
13g.108209216A>TCA388614237LIG4c.1852T>A (p.Phe618Ile)
c.2053T>A (p.Phe685Ile)
c.2089T>A (p.Phe697Ile)
c.2065T>A (p.Phe689Ile)
13g.108209217T>ACA388614239LIG4c.1851A>T (p.Glu617Asp)
c.2052A>T (p.Glu684Asp)
c.2088A>T (p.Glu696Asp)
c.2064A>T (p.Glu688Asp)
13g.108209217T>CCA484975479LIG4c.1851A>G (p.Glu617=)
c.2052A>G (p.Glu684=)
c.2088A>G (p.Glu696=)
c.2064A>G (p.Glu688=)
13g.108209217T>GCA388614241LIG4c.1851A>C (p.Glu617Asp)
c.2052A>C (p.Glu684Asp)
c.2088A>C (p.Glu696Asp)
c.2064A>C (p.Glu688Asp)
13g.108209218T>ACA388614244LIG4c.1850A>T (p.Glu617Val)
c.2051A>T (p.Glu684Val)
c.2087A>T (p.Glu696Val)
c.2063A>T (p.Glu688Val)
13g.108209218T>CCA388614246LIG4c.1850A>G (p.Glu617Gly)
c.2051A>G (p.Glu684Gly)
c.2087A>G (p.Glu696Gly)
c.2063A>G (p.Glu688Gly)
13g.108209218T>GCA388614249LIG4c.1850A>C (p.Glu617Ala)
c.2051A>C (p.Glu684Ala)
c.2087A>C (p.Glu696Ala)
c.2063A>C (p.Glu688Ala)
 gnomAD v4
13g.108209219C>ACA388614259LIG4c.1849G>T (p.Glu617Ter)
c.2050G>T (p.Glu684Ter)
c.2086G>T (p.Glu696Ter)
c.2062G>T (p.Glu688Ter)
13g.108209219C=CA2117794092LIG4c.1849G= (p.Glu617=)
c.2050G= (p.Glu684=)
c.2086G= (p.Glu696=)
c.2062G= (p.Glu688=)
13g.108209219C>GCA388614253LIG4c.1849G>C (p.Glu617Gln)
c.2050G>C (p.Glu684Gln)
c.2086G>C (p.Glu696Gln)
c.2062G>C (p.Glu688Gln)
 dbSNP
13g.108209219C>TCA7043563LIG4c.1849G>A (p.Glu617Lys)
c.2050G>A (p.Glu684Lys)
c.2086G>A (p.Glu696Lys)
c.2062G>A (p.Glu688Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.108209220T>ACA484975092LIG4c.1848A>T (p.Ala616=)
c.2049A>T (p.Ala683=)
c.2085A>T (p.Ala695=)
c.2061A>T (p.Ala687=)
13g.108209220T>CCA484975097LIG4c.1848A>G (p.Ala616=)
c.2049A>G (p.Ala683=)
c.2085A>G (p.Ala695=)
c.2061A>G (p.Ala687=)
13g.108209220T>GCA484975095LIG4c.1848A>C (p.Ala616=)
c.2049A>C (p.Ala683=)
c.2085A>C (p.Ala695=)
c.2061A>C (p.Ala687=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.108209220T=CA2117794093LIG4c.1848A= (p.Ala616=)
c.2049A= (p.Ala683=)
c.2085A= (p.Ala695=)
c.2061A= (p.Ala687=)
13g.108209221G>ACA388614261LIG4c.1847C>T (p.Ala616Val)
c.2048C>T (p.Ala683Val)
c.2084C>T (p.Ala695Val)
c.2060C>T (p.Ala687Val)
 dbSNP gnomAD v3 gnomAD v4
13g.108209221G>CCA388614262LIG4c.1847C>G (p.Ala616Gly)
c.2048C>G (p.Ala683Gly)
c.2084C>G (p.Ala695Gly)
c.2060C>G (p.Ala687Gly)
 dbSNP
13g.108209221G=CA2117794094LIG4c.1847C= (p.Ala616=)
c.2048C= (p.Ala683=)
c.2084C= (p.Ala695=)
c.2060C= (p.Ala687=)
13g.108209221G>TCA388614263LIG4c.1847C>A (p.Ala616Glu)
c.2048C>A (p.Ala683Glu)
c.2084C>A (p.Ala695Glu)
c.2060C>A (p.Ala687Glu)
13g.108209222C>ACA388614266LIG4c.1846G>T (p.Ala616Ser)
c.2047G>T (p.Ala683Ser)
c.2083G>T (p.Ala695Ser)
c.2059G>T (p.Ala687Ser)
13g.108209222C>GCA388614269LIG4c.1846G>C (p.Ala616Pro)
c.2047G>C (p.Ala683Pro)
c.2083G>C (p.Ala695Pro)
c.2059G>C (p.Ala687Pro)
13g.108209222C>TCA388614271LIG4c.1846G>A (p.Ala616Thr)
c.2047G>A (p.Ala683Thr)
c.2083G>A (p.Ala695Thr)
c.2059G>A (p.Ala687Thr)
13g.108209223A>CCA388614274LIG4c.1845T>G (p.Ile615Met)
c.2046T>G (p.Ile682Met)
c.2082T>G (p.Ile694Met)
c.2058T>G (p.Ile686Met)
 ClinVar dbSNP
13g.108209223A>GCA484975099LIG4c.1845T>C (p.Ile615=)
c.2046T>C (p.Ile682=)
c.2082T>C (p.Ile694=)
c.2058T>C (p.Ile686=)
13g.108209223A>TCA484975100LIG4c.1845T>A (p.Ile615=)
c.2046T>A (p.Ile682=)
c.2082T>A (p.Ile694=)
c.2058T>A (p.Ile686=)
13g.108209224A=CA2117794095LIG4c.1844T= (p.Ile615=)
c.2045T= (p.Ile682=)
c.2081T= (p.Ile694=)
c.2057T= (p.Ile686=)
13g.108209224A>CCA388614277LIG4c.1844T>G (p.Ile615Ser)
c.2045T>G (p.Ile682Ser)
c.2081T>G (p.Ile694Ser)
c.2057T>G (p.Ile686Ser)
13g.108209224A>GCA7043564LIG4c.1844T>C (p.Ile615Thr)
c.2045T>C (p.Ile682Thr)
c.2081T>C (p.Ile694Thr)
c.2057T>C (p.Ile686Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.108209224A>TCA388614278LIG4c.1844T>A (p.Ile615Asn)
c.2045T>A (p.Ile682Asn)
c.2081T>A (p.Ile694Asn)
c.2057T>A (p.Ile686Asn)
13g.108209225T>ACA388614279LIG4c.1843A>T (p.Ile615Phe)
c.2044A>T (p.Ile682Phe)
c.2080A>T (p.Ile694Phe)
c.2056A>T (p.Ile686Phe)
13g.108209225T>CCA388614283LIG4c.1843A>G (p.Ile615Val)
c.2044A>G (p.Ile682Val)
c.2080A>G (p.Ile694Val)
c.2056A>G (p.Ile686Val)
13g.108209225T>GCA7043565LIG4c.1843A>C (p.Ile615Leu)
c.2044A>C (p.Ile682Leu)
c.2080A>C (p.Ile694Leu)
c.2056A>C (p.Ile686Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.108209225T=CA2117794096LIG4c.1843A= (p.Ile615=)
c.2044A= (p.Ile682=)
c.2080A= (p.Ile694=)
c.2056A= (p.Ile686=)
13g.108209226T>ACA388614287LIG4c.1842A>T (p.Arg614Ser)
c.2043A>T (p.Arg681Ser)
c.2079A>T (p.Arg693Ser)
c.2055A>T (p.Arg685Ser)
13g.108209226T>CCA484975103LIG4c.1842A>G (p.Arg614=)
c.2043A>G (p.Arg681=)
c.2079A>G (p.Arg693=)
c.2055A>G (p.Arg685=)
13g.108209226T>GCA388614290LIG4c.1842A>C (p.Arg614Ser)
c.2043A>C (p.Arg681Ser)
c.2079A>C (p.Arg693Ser)
c.2055A>C (p.Arg685Ser)
13g.108209227C>ACA388614293LIG4c.1841G>T (p.Arg614Ile)
c.2042G>T (p.Arg681Ile)
c.2078G>T (p.Arg693Ile)
c.2054G>T (p.Arg685Ile)
 COSMIC
13g.108209227C=CA2117794097LIG4c.1841G= (p.Arg614=)
c.2042G= (p.Arg681=)
c.2078G= (p.Arg693=)
c.2054G= (p.Arg685=)
13g.108209227C>GCA388614299LIG4c.1841G>C (p.Arg614Thr)
c.2042G>C (p.Arg681Thr)
c.2078G>C (p.Arg693Thr)
c.2054G>C (p.Arg685Thr)
13g.108209227C>TCA7043566LIG4c.1841G>A (p.Arg614Lys)
c.2042G>A (p.Arg681Lys)
c.2078G>A (p.Arg693Lys)
c.2054G>A (p.Arg685Lys)
 ClinVar dbSNP ExAC gnomAD v2
13g.108209228T>ACA7043567LIG4c.1840A>T (p.Arg614Ter)
c.2041A>T (p.Arg681Ter)
c.2077A>T (p.Arg693Ter)
c.2053A>T (p.Arg685Ter)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.108209228T>CCA388614302LIG4c.1840A>G (p.Arg614Gly)
c.2041A>G (p.Arg681Gly)
c.2077A>G (p.Arg693Gly)
c.2053A>G (p.Arg685Gly)
 dbSNP
13g.108209228T>GCA484975106LIG4c.1840A>C (p.Arg614=)
c.2041A>C (p.Arg681=)
c.2077A>C (p.Arg693=)
c.2053A>C (p.Arg685=)
 gnomAD v4
13g.108209228T=CA2117794098LIG4c.1840A= (p.Arg614=)
c.2041A= (p.Arg681=)
c.2077A= (p.Arg693=)
c.2053A= (p.Arg685=)
13g.108209229G>ACA484975108LIG4c.1839C>T (p.Asn613=)
c.2040C>T (p.Asn680=)
c.2076C>T (p.Asn692=)
c.2052C>T (p.Asn684=)
 ClinVar gnomAD v4
13g.108209229G>CCA388614303LIG4c.1839C>G (p.Asn613Lys)
c.2040C>G (p.Asn680Lys)
c.2076C>G (p.Asn692Lys)
c.2052C>G (p.Asn684Lys)
13g.108209229G>TCA388614305LIG4c.1839C>A (p.Asn613Lys)
c.2040C>A (p.Asn680Lys)
c.2076C>A (p.Asn692Lys)
c.2052C>A (p.Asn684Lys)
13g.108209230T>ACA388614310LIG4c.1838A>T (p.Asn613Ile)
c.2039A>T (p.Asn680Ile)
c.2075A>T (p.Asn692Ile)
c.2051A>T (p.Asn684Ile)
13g.108209230T>CCA256180176LIG4c.1838A>G (p.Asn613Ser)
c.2039A>G (p.Asn680Ser)
c.2075A>G (p.Asn692Ser)
c.2051A>G (p.Asn684Ser)
 dbSNP
13g.108209230T>GCA388614313LIG4c.1838A>C (p.Asn613Thr)
c.2039A>C (p.Asn680Thr)
c.2075A>C (p.Asn692Thr)
c.2051A>C (p.Asn684Thr)
 dbSNP
13g.108209230T=CA2117794099LIG4c.1838A= (p.Asn613=)
c.2039A= (p.Asn680=)
c.2075A= (p.Asn692=)
c.2051A= (p.Asn684=)
13g.108209231T>ACA388614315LIG4c.1837A>T (p.Asn613Tyr)
c.2038A>T (p.Asn680Tyr)
c.2074A>T (p.Asn692Tyr)
c.2050A>T (p.Asn684Tyr)
13g.108209231T>CCA388614318LIG4c.1837A>G (p.Asn613Asp)
c.2038A>G (p.Asn680Asp)
c.2074A>G (p.Asn692Asp)
c.2050A>G (p.Asn684Asp)
 ClinVar dbSNP gnomAD v4
13g.108209231T>GCA388614327LIG4c.1837A>C (p.Asn613His)
c.2038A>C (p.Asn680His)
c.2074A>C (p.Asn692His)
c.2050A>C (p.Asn684His)
13g.108209232C>ACA388614333LIG4c.1836G>T (p.Glu612Asp)
c.2037G>T (p.Glu679Asp)
c.2073G>T (p.Glu691Asp)
c.2049G>T (p.Glu683Asp)
13g.108209232C>GCA388614336LIG4c.1836G>C (p.Glu612Asp)
c.2037G>C (p.Glu679Asp)
c.2073G>C (p.Glu691Asp)
c.2049G>C (p.Glu683Asp)
13g.108209232C>TCA484975118LIG4c.1836G>A (p.Glu612=)
c.2037G>A (p.Glu679=)
c.2073G>A (p.Glu691=)
c.2049G>A (p.Glu683=)
13g.108209233T>ACA388614339LIG4c.1835A>T (p.Glu612Val)
c.2036A>T (p.Glu679Val)
c.2072A>T (p.Glu691Val)
c.2048A>T (p.Glu683Val)
13g.108209233T>CCA388614344LIG4c.1835A>G (p.Glu612Gly)
c.2036A>G (p.Glu679Gly)
c.2072A>G (p.Glu691Gly)
c.2048A>G (p.Glu683Gly)
13g.108209233T>GCA388614342LIG4c.1835A>C (p.Glu612Ala)
c.2036A>C (p.Glu679Ala)
c.2072A>C (p.Glu691Ala)
c.2048A>C (p.Glu683Ala)
13g.108209234C>ACA388614348LIG4c.1834G>T (p.Glu612Ter)
c.2035G>T (p.Glu679Ter)
c.2071G>T (p.Glu691Ter)
c.2047G>T (p.Glu683Ter)
13g.108209234C=CA2117794100LIG4c.1834G= (p.Glu612=)
c.2035G= (p.Glu679=)
c.2071G= (p.Glu691=)
c.2047G= (p.Glu683=)
13g.108209234C>GCA256180199LIG4c.1834G>C (p.Glu612Gln)
c.2035G>C (p.Glu679Gln)
c.2071G>C (p.Glu691Gln)
c.2047G>C (p.Glu683Gln)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.108209234C>TCA388614360LIG4c.1834G>A (p.Glu612Lys)
c.2035G>A (p.Glu679Lys)
c.2071G>A (p.Glu691Lys)
c.2047G>A (p.Glu683Lys)
 ClinVar dbSNP gnomAD v4
13g.108209235C>ACA484975122LIG4c.1833G>T (p.Leu611=)
c.2034G>T (p.Leu678=)
c.2070G>T (p.Leu690=)
c.2046G>T (p.Leu682=)
13g.108209235C>GCA484975124LIG4c.1833G>C (p.Leu611=)
c.2034G>C (p.Leu678=)
c.2070G>C (p.Leu690=)
c.2046G>C (p.Leu682=)
13g.108209235C>TCA484975125LIG4c.1833G>A (p.Leu611=)
c.2034G>A (p.Leu678=)
c.2070G>A (p.Leu690=)
c.2046G>A (p.Leu682=)
13g.108209236A>CCA388614366LIG4c.1832T>G (p.Leu611Arg)
c.2033T>G (p.Leu678Arg)
c.2069T>G (p.Leu690Arg)
c.2045T>G (p.Leu682Arg)
13g.108209236A>GCA388614369LIG4c.1832T>C (p.Leu611Pro)
c.2033T>C (p.Leu678Pro)
c.2069T>C (p.Leu690Pro)
c.2045T>C (p.Leu682Pro)
13g.108209236A>TCA388614371LIG4c.1832T>A (p.Leu611Gln)
c.2033T>A (p.Leu678Gln)
c.2069T>A (p.Leu690Gln)
c.2045T>A (p.Leu682Gln)
13g.108209237G>ACA484975126LIG4c.1831C>T (p.Leu611=)
c.2032C>T (p.Leu678=)
c.2068C>T (p.Leu690=)
c.2044C>T (p.Leu682=)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
13g.108209237G>CCA388614375LIG4c.1831C>G (p.Leu611Val)
c.2032C>G (p.Leu678Val)
c.2068C>G (p.Leu690Val)
c.2044C>G (p.Leu682Val)
 dbSNP gnomAD v2 gnomAD v4
13g.108209237G=CA2117794101LIG4c.1831C= (p.Leu611=)
c.2032C= (p.Leu678=)
c.2068C= (p.Leu690=)
c.2044C= (p.Leu682=)
13g.108209237G>TCA388614389LIG4c.1831C>A (p.Leu611Met)
c.2032C>A (p.Leu678Met)
c.2068C>A (p.Leu690Met)
c.2044C>A (p.Leu682Met)
 gnomAD v4
13g.108209238G>ACA484975128LIG4c.1830C>T (p.Asp610=)
c.2031C>T (p.Asp677=)
c.2067C>T (p.Asp689=)
c.2043C>T (p.Asp681=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.108209238G>CCA388614393LIG4c.1830C>G (p.Asp610Glu)
c.2031C>G (p.Asp677Glu)
c.2067C>G (p.Asp689Glu)
c.2043C>G (p.Asp681Glu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.108209238G=CA2117794102LIG4c.1830C= (p.Asp610=)
c.2031C= (p.Asp677=)
c.2067C= (p.Asp689=)
c.2043C= (p.Asp681=)
13g.108209238G>TCA388614397LIG4c.1830C>A (p.Asp610Glu)
c.2031C>A (p.Asp677Glu)
c.2067C>A (p.Asp689Glu)
c.2043C>A (p.Asp681Glu)
13g.108209239T>ACA388614409LIG4c.1829A>T (p.Asp610Val)
c.2030A>T (p.Asp677Val)
c.2066A>T (p.Asp689Val)
c.2042A>T (p.Asp681Val)
13g.108209239T>CCA388614410LIG4c.1829A>G (p.Asp610Gly)
c.2030A>G (p.Asp677Gly)
c.2066A>G (p.Asp689Gly)
c.2042A>G (p.Asp681Gly)
13g.108209239T>GCA388614406LIG4c.1829A>C (p.Asp610Ala)
c.2030A>C (p.Asp677Ala)
c.2066A>C (p.Asp689Ala)
c.2042A>C (p.Asp681Ala)
13g.108209240C>ACA388614411LIG4c.1828G>T (p.Asp610Tyr)
c.2029G>T (p.Asp677Tyr)
c.2065G>T (p.Asp689Tyr)
c.2041G>T (p.Asp681Tyr)
13g.108209240C>GCA388614416LIG4c.1828G>C (p.Asp610His)
c.2029G>C (p.Asp677His)
c.2065G>C (p.Asp689His)
c.2041G>C (p.Asp681His)
13g.108209240C>TCA388614418LIG4c.1828G>A (p.Asp610Asn)
c.2029G>A (p.Asp677Asn)
c.2065G>A (p.Asp689Asn)
c.2041G>A (p.Asp681Asn)
 COSMIC
13g.108209241A=CA2117794103LIG4c.1827T= (p.Pro609=)
c.2028T= (p.Pro676=)
c.2064T= (p.Pro688=)
c.2040T= (p.Pro680=)
13g.108209241A>CCA484975135LIG4c.1827T>G (p.Pro609=)
c.2028T>G (p.Pro676=)
c.2064T>G (p.Pro688=)
c.2040T>G (p.Pro680=)
13g.108209241A>GCA484975134LIG4c.1827T>C (p.Pro609=)
c.2028T>C (p.Pro676=)
c.2064T>C (p.Pro688=)
c.2040T>C (p.Pro680=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.108209241A>TCA484975133LIG4c.1827T>A (p.Pro609=)
c.2028T>A (p.Pro676=)
c.2064T>A (p.Pro688=)
c.2040T>A (p.Pro680=)
 dbSNP
13g.108209242G>ACA388614420LIG4c.1826C>T (p.Pro609Leu)
c.2027C>T (p.Pro676Leu)
c.2063C>T (p.Pro688Leu)
c.2039C>T (p.Pro680Leu)
13g.108209242G>CCA388614423LIG4c.1826C>G (p.Pro609Arg)
c.2027C>G (p.Pro676Arg)
c.2063C>G (p.Pro688Arg)
c.2039C>G (p.Pro680Arg)
13g.108209242G>TCA388614425LIG4c.1826C>A (p.Pro609His)
c.2027C>A (p.Pro676His)
c.2063C>A (p.Pro688His)
c.2039C>A (p.Pro680His)
13g.108209243G>ACA388614433LIG4c.1825C>T (p.Pro609Ser)
c.2026C>T (p.Pro676Ser)
c.2062C>T (p.Pro688Ser)
c.2038C>T (p.Pro680Ser)
 dbSNP
13g.108209243G>CCA388614429LIG4c.1825C>G (p.Pro609Ala)
c.2026C>G (p.Pro676Ala)
c.2062C>G (p.Pro688Ala)
c.2038C>G (p.Pro680Ala)
13g.108209243G=CA2117794104LIG4c.1825C= (p.Pro609=)
c.2026C= (p.Pro676=)
c.2062C= (p.Pro688=)
c.2038C= (p.Pro680=)
13g.108209243G>TCA388614432LIG4c.1825C>A (p.Pro609Thr)
c.2026C>A (p.Pro676Thr)
c.2062C>A (p.Pro688Thr)
c.2038C>A (p.Pro680Thr)
13g.108209244C>ACA388614435LIG4c.1824G>T (p.Lys608Asn)
c.2025G>T (p.Lys675Asn)
c.2061G>T (p.Lys687Asn)
c.2037G>T (p.Lys679Asn)
13g.108209244C>GCA388614437LIG4c.1824G>C (p.Lys608Asn)
c.2025G>C (p.Lys675Asn)
c.2061G>C (p.Lys687Asn)
c.2037G>C (p.Lys679Asn)
13g.108209244C>TCA484975144LIG4c.1824G>A (p.Lys608=)
c.2025G>A (p.Lys675=)
c.2061G>A (p.Lys687=)
c.2037G>A (p.Lys679=)
13g.108209245T>ACA388614441LIG4c.1823A>T (p.Lys608Met)
c.2024A>T (p.Lys675Met)
c.2060A>T (p.Lys687Met)
c.2036A>T (p.Lys679Met)
13g.108209245T>CCA388614446LIG4c.1823A>G (p.Lys608Arg)
c.2024A>G (p.Lys675Arg)
c.2060A>G (p.Lys687Arg)
c.2036A>G (p.Lys679Arg)
13g.108209245T>GCA388614447LIG4c.1823A>C (p.Lys608Thr)
c.2024A>C (p.Lys675Thr)
c.2060A>C (p.Lys687Thr)
c.2036A>C (p.Lys679Thr)

Number of alleles fetched