Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.68695781_68695782del | CA283289368 | CDH3 | c.2138_2139del (p.Tyr713Ter) c.*1876_*1877del (n.*1876_*1877del) c.468_469del c.217_218del c.1973_1974del (p.Tyr658Ter) | dbSNP |
16 | g.68695782T>A | CA396456167 | CDH3 | c.2139T>A (p.Tyr713Ter) c.*1877T>A (n.*1877T>A) c.469T>A c.218T>A c.1974T>A (p.Tyr658Ter) | COSMIC COSMIC |
16 | g.68695782T>C | CA8129596 | CDH3 | c.2139T>C (p.Tyr713=) c.*1877T>C (n.*1877T>C) c.469T>C c.218T>C c.1974T>C (p.Tyr658=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.68695782T>G | CA396456168 | CDH3 | c.2139T>G (p.Tyr713Ter) c.*1877T>G (n.*1877T>G) c.469T>G c.218T>G c.1974T>G (p.Tyr658Ter) | dbSNP gnomAD v4 |
16 | g.68695782T= | CA2229920413 | CDH3 | c.2139T= (p.Tyr713=) c.*1877T= (n.*1877T=) c.469T= c.218T= c.1974T= (p.Tyr658=) | |
16 | g.68695783G>A | CA396456169 | CDH3 | c.2140G>A (p.Asp714Asn) c.*1878G>A (n.*1878G>A) c.470G>A c.219G>A c.1975G>A (p.Asp659Asn) | |
16 | g.68695783G>C | CA396456170 | CDH3 | c.2140G>C (p.Asp714His) c.*1878G>C (n.*1878G>C) c.470G>C c.219G>C c.1975G>C (p.Asp659His) | |
16 | g.68695783G>T | CA396456171 | CDH3 | c.2140G>T (p.Asp714Tyr) c.*1878G>T (n.*1878G>T) c.470G>T c.219G>T c.1975G>T (p.Asp659Tyr) | |
16 | g.68695784A>C | CA396456172 | CDH3 | c.2141A>C (p.Asp714Ala) c.*1879A>C (n.*1879A>C) c.471A>C c.220A>C c.1976A>C (p.Asp659Ala) | |
16 | g.68695784A>G | CA396456174 | CDH3 | c.2141A>G (p.Asp714Gly) c.*1879A>G (n.*1879A>G) c.471A>G c.220A>G c.1976A>G (p.Asp659Gly) | |
16 | g.68695784A>T | CA396456173 | CDH3 | c.2141A>T (p.Asp714Val) c.*1879A>T (n.*1879A>T) c.471A>T c.220A>T c.1976A>T (p.Asp659Val) | |
16 | g.68695785C>A | CA8129598 | CDH3 | c.2142C>A (p.Asp714Glu) c.*1880C>A (n.*1880C>A) c.472C>A c.221C>A c.1977C>A (p.Asp659Glu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695785C= | CA2229920415 | CDH3 | c.2142C= (p.Asp714=) c.*1880C= (n.*1880C=) c.472C= c.221C= c.1977C= (p.Asp659=) | |
16 | g.68695785C>G | CA396456175 | CDH3 | c.2142C>G (p.Asp714Glu) c.*1880C>G (n.*1880C>G) c.472C>G c.221C>G c.1977C>G (p.Asp659Glu) | |
16 | g.68695785C>T | CA8129597 | CDH3 | c.2142C>T (p.Asp714=) c.*1880C>T (n.*1880C>T) c.472C>T c.221C>T c.1977C>T (p.Asp659=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.68695786A>C | CA396456176 | CDH3 | c.2143A>C (p.Ile715Leu) c.*1881A>C (n.*1881A>C) c.473A>C c.222A>C c.1978A>C (p.Ile660Leu) | |
16 | g.68695786A>G | CA396456177 | CDH3 | c.2143A>G (p.Ile715Val) c.*1881A>G (n.*1881A>G) c.473A>G c.222A>G c.1978A>G (p.Ile660Val) | |
16 | g.68695786A>T | CA396456178 | CDH3 | c.2143A>T (p.Ile715Phe) c.*1881A>T (n.*1881A>T) c.473A>T c.222A>T c.1978A>T (p.Ile660Phe) | |
16 | g.68695787T>A | CA396456179 | CDH3 | c.2144T>A (p.Ile715Asn) c.*1882T>A (n.*1882T>A) c.474T>A c.223T>A c.1979T>A (p.Ile660Asn) | |
16 | g.68695787T>C | CA396456180 | CDH3 | c.2144T>C (p.Ile715Thr) c.*1882T>C (n.*1882T>C) c.474T>C c.223T>C c.1979T>C (p.Ile660Thr) | |
16 | g.68695787T>G | CA396456181 | CDH3 | c.2144T>G (p.Ile715Ser) c.*1882T>G (n.*1882T>G) c.474T>G c.223T>G c.1979T>G (p.Ile660Ser) | |
16 | g.68695788C>A | CA496157706 | CDH3 | c.2145C>A (p.Ile715=) c.*1883C>A (n.*1883C>A) c.475C>A c.224C>A c.1980C>A (p.Ile660=) | |
16 | g.68695788C>G | CA396456182 | CDH3 | c.2145C>G (p.Ile715Met) c.*1883C>G (n.*1883C>G) c.475C>G c.224C>G c.1980C>G (p.Ile660Met) | |
16 | g.68695788C>T | CA496157707 | CDH3 | c.2145C>T (p.Ile715=) c.*1883C>T (n.*1883C>T) c.475C>T c.224C>T c.1980C>T (p.Ile660=) | gnomAD v4 |
16 | g.68695789A>C | CA396456185 | CDH3 | c.2146A>C (p.Thr716Pro) c.*1884A>C (n.*1884A>C) c.476A>C c.225A>C c.1981A>C (p.Thr661Pro) | |
16 | g.68695789A>G | CA396456184 | CDH3 | c.2146A>G (p.Thr716Ala) c.*1884A>G (n.*1884A>G) c.476A>G c.225A>G c.1981A>G (p.Thr661Ala) | |
16 | g.68695789A>T | CA396456183 | CDH3 | c.2146A>T (p.Thr716Ser) c.*1884A>T (n.*1884A>T) c.476A>T c.225A>T c.1981A>T (p.Thr661Ser) | |
16 | g.68695790C>A | CA396456186 | CDH3 | c.2147C>A (p.Thr716Asn) c.*1885C>A (n.*1885C>A) c.477C>A c.226C>A c.1982C>A (p.Thr661Asn) | |
16 | g.68695790C= | CA2229920418 | CDH3 | c.2147C= (p.Thr716=) c.*1885C= (n.*1885C=) c.477C= c.226C= c.1982C= (p.Thr661=) | |
16 | g.68695790C>G | CA396456187 | CDH3 | c.2147C>G (p.Thr716Ser) c.*1885C>G (n.*1885C>G) c.477C>G c.226C>G c.1982C>G (p.Thr661Ser) | |
16 | g.68695790C>T | CA8129599 | CDH3 | c.2147C>T (p.Thr716Ile) c.*1885C>T (n.*1885C>T) c.477C>T c.226C>T c.1982C>T (p.Thr661Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695791C>A | CA496157708 | CDH3 | c.2148C>A (p.Thr716=) c.*1886C>A (n.*1886C>A) c.478C>A c.227C>A c.1983C>A (p.Thr661=) | |
16 | g.68695791C= | CA2229920420 | CDH3 | c.2148C= (p.Thr716=) c.*1886C= (n.*1886C=) c.478C= c.227C= c.1983C= (p.Thr661=) | |
16 | g.68695791C>G | CA496157709 | CDH3 | c.2148C>G (p.Thr716=) c.*1886C>G (n.*1886C>G) c.478C>G c.227C>G c.1983C>G (p.Thr661=) | |
16 | g.68695791C>T | CA8129600 | CDH3 | c.2148C>T (p.Thr716=) c.*1886C>T (n.*1886C>T) c.478C>T c.227C>T c.1983C>T (p.Thr661=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.68695792C>A | CA396456188 | CDH3 | c.2149C>A (p.Gln717Lys) c.*1887C>A (n.*1887C>A) c.479C>A c.228C>A c.1984C>A (p.Gln662Lys) | |
16 | g.68695792C>G | CA396456189 | CDH3 | c.2149C>G (p.Gln717Glu) c.*1887C>G (n.*1887C>G) c.479C>G c.228C>G c.1984C>G (p.Gln662Glu) | |
16 | g.68695792C>T | CA396456190 | CDH3 | c.2149C>T (p.Gln717Ter) c.*1887C>T (n.*1887C>T) c.479C>T c.228C>T c.1984C>T (p.Gln662Ter) | |
16 | g.68695793A= | CA2229920422 | CDH3 | c.2150A= (p.Gln717=) c.*1888A= (n.*1888A=) c.480A= c.229A= c.1985A= (p.Gln662=) | |
16 | g.68695793A>C | CA396456191 | CDH3 | c.2150A>C (p.Gln717Pro) c.*1888A>C (n.*1888A>C) c.480A>C c.229A>C c.1985A>C (p.Gln662Pro) | |
16 | g.68695793A>G | CA396456192 | CDH3 | c.2150A>G (p.Gln717Arg) c.*1888A>G (n.*1888A>G) c.480A>G c.229A>G c.1985A>G (p.Gln662Arg) | |
16 | g.68695793A>T | CA396456193 | CDH3 | c.2150A>T (p.Gln717Leu) c.*1888A>T (n.*1888A>T) c.480A>T c.229A>T c.1985A>T (p.Gln662Leu) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.68695794G>A | CA496157710 | CDH3 | c.2151G>A (p.Gln717=) c.*1889G>A (n.*1889G>A) c.481G>A c.230G>A c.1986G>A (p.Gln662=) | gnomAD v4 |
16 | g.68695794G>C | CA396456194 | CDH3 | c.2151G>C (p.Gln717His) c.*1889G>C (n.*1889G>C) c.481G>C c.230G>C c.1986G>C (p.Gln662His) | |
16 | g.68695794G>T | CA396456195 | CDH3 | c.2151G>T (p.Gln717His) c.*1889G>T (n.*1889G>T) c.481G>T c.230G>T c.1986G>T (p.Gln662His) | |
16 | g.68695794dup | CA2633928519 | CDH3 | c.2151dup (p.Leu718AlafsTer16) c.*1889dup (n.*1889dup) c.481dup c.230dup c.1986dup (p.Leu663AlafsTer16) | gnomAD v4 |
16 | g.68695795C>A | CA396456197 | CDH3 | c.2152C>A (p.Leu718Ile) c.*1890C>A (n.*1890C>A) c.482C>A c.231C>A c.1987C>A (p.Leu663Ile) | |
16 | g.68695795C>G | CA396456198 | CDH3 | c.2152C>G (p.Leu718Val) c.*1890C>G (n.*1890C>G) c.482C>G c.231C>G c.1987C>G (p.Leu663Val) | |
16 | g.68695795C>T | CA396456196 | CDH3 | c.2152C>T (p.Leu718Phe) c.*1890C>T (n.*1890C>T) c.482C>T c.231C>T c.1987C>T (p.Leu663Phe) | |
16 | g.68695795_68695796insCGGAG | CA2633928523 | CDH3 | c.2152_2153insCGGAG (p.Leu718ProfsTer?) c.*1890_*1891insCGGAG (n.*1890_*1891insCGGAG) c.482_483insCGGAG c.231_232insCGGAG c.1987_1988insCGGAG (p.Leu663ProfsTer?) | gnomAD v4 |
16 | g.68695796T>A | CA396456199 | CDH3 | c.2153T>A (p.Leu718His) c.*1891T>A (n.*1891T>A) c.483T>A c.232T>A c.1988T>A (p.Leu663His) | |
16 | g.68695796T>C | CA396456200 | CDH3 | c.2153T>C (p.Leu718Pro) c.*1891T>C (n.*1891T>C) c.483T>C c.232T>C c.1988T>C (p.Leu663Pro) | gnomAD v4 |
16 | g.68695796T>G | CA396456201 | CDH3 | c.2153T>G (p.Leu718Arg) c.*1891T>G (n.*1891T>G) c.483T>G c.232T>G c.1988T>G (p.Leu663Arg) | |
16 | g.68695797C>A | CA496157711 | CDH3 | c.2154C>A (p.Leu718=) c.*1892C>A (n.*1892C>A) c.484C>A c.233C>A c.1989C>A (p.Leu663=) | |
16 | g.68695797C>G | CA496157712 | CDH3 | c.2154C>G (p.Leu718=) c.*1892C>G (n.*1892C>G) c.484C>G c.233C>G c.1989C>G (p.Leu663=) | |
16 | g.68695797C>T | CA496157713 | CDH3 | c.2154C>T (p.Leu718=) c.*1892C>T (n.*1892C>T) c.484C>T c.233C>T c.1989C>T (p.Leu663=) | |
16 | g.68695797_68695798insA | CA2633928529 | CDH3 | c.2154_2155insA (p.His719ThrfsTer15) c.*1892_*1893insA (n.*1892_*1893insA) c.484_485insA c.233_234insA c.1989_1990insA (p.His664ThrfsTer15) | gnomAD v4 |
16 | g.68695798C>A | CA396456202 | CDH3 | c.2155C>A (p.His719Asn) c.*1893C>A (n.*1893C>A) c.485C>A c.234C>A c.1990C>A (p.His664Asn) | |
16 | g.68695798C= | CA2229920425 | CDH3 | c.2155C= (p.His719=) c.*1893C= (n.*1893C=) c.485C= c.234C= c.1990C= (p.His664=) | |
16 | g.68695798C>G | CA396456203 | CDH3 | c.2155C>G (p.His719Asp) c.*1893C>G (n.*1893C>G) c.485C>G c.234C>G c.1990C>G (p.His664Asp) | |
16 | g.68695798C>T | CA396456204 | CDH3 | c.2155C>T (p.His719Tyr) c.*1893C>T (n.*1893C>T) c.485C>T c.234C>T c.1990C>T (p.His664Tyr) | ClinVar dbSNP gnomAD v4 |
16 | g.68695799A= | CA2229920427 | CDH3 | c.2156A= (p.His719=) c.*1894A= (n.*1894A=) c.486A= c.235A= c.1991A= (p.His664=) | |
16 | g.68695799A>C | CA396456205 | CDH3 | c.2156A>C (p.His719Pro) c.*1894A>C (n.*1894A>C) c.486A>C c.235A>C c.1991A>C (p.His664Pro) | |
16 | g.68695799A>G | CA283289386 | CDH3 | c.2156A>G (p.His719Arg) c.*1894A>G (n.*1894A>G) c.486A>G c.235A>G c.1991A>G (p.His664Arg) | dbSNP gnomAD v4 |
16 | g.68695799A>T | CA396456206 | CDH3 | c.2156A>T (p.His719Leu) c.*1894A>T (n.*1894A>T) c.486A>T c.235A>T c.1991A>T (p.His664Leu) | |
16 | g.68695799_68695800insGGACT | CA2633928539 | CDH3 | c.2156_2157insGGACT (p.His719GlnfsTer?) c.*1894_*1895insGGACT (n.*1894_*1895insGGACT) c.486_487insGGACT c.235_236insGGACT c.1991_1992insGGACT (p.His664GlnfsTer?) | gnomAD v4 |
16 | g.68695800C>A | CA396456207 | CDH3 | c.2157C>A (p.His719Gln) c.*1895C>A (n.*1895C>A) c.487C>A c.236C>A c.1992C>A (p.His664Gln) | |
16 | g.68695800C= | CA2229920429 | CDH3 | c.2157C= (p.His719=) c.*1895C= (n.*1895C=) c.487C= c.236C= c.1992C= (p.His664=) | |
16 | g.68695800C>G | CA396456208 | CDH3 | c.2157C>G (p.His719Gln) c.*1895C>G (n.*1895C>G) c.487C>G c.236C>G c.1992C>G (p.His664Gln) | |
16 | g.68695800C>T | CA496157714 | CDH3 | c.2157C>T (p.His719=) c.*1895C>T (n.*1895C>T) c.487C>T c.236C>T c.1992C>T (p.His664=) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.68695801C>A | CA496157715 | CDH3 | c.2158C>A (p.Arg720=) c.*1896C>A (n.*1896C>A) c.488C>A c.237C>A c.1993C>A (p.Arg665=) | |
16 | g.68695801C= | CA2229920432 | CDH3 | c.2158C= (p.Arg720=) c.*1896C= (n.*1896C=) c.488C= c.237C= c.1993C= (p.Arg665=) | |
16 | g.68695801C>G | CA8129602 | CDH3 | c.2158C>G (p.Arg720Gly) c.*1896C>G (n.*1896C>G) c.488C>G c.237C>G c.1993C>G (p.Arg665Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695801C>T | CA8129601 | CDH3 | c.2158C>T (p.Arg720Ter) c.*1896C>T (n.*1896C>T) c.488C>T c.237C>T c.1993C>T (p.Arg665Ter) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.68695802del | CA2633928561 | CDH3 | c.2159del (p.Arg720GlnfsTer?) c.*1897del (n.*1897del) c.489del c.238del c.1994del (p.Arg665GlnfsTer?) | gnomAD v4 |
16 | g.68695802G>A | CA8129603 | CDH3 | c.2159G>A (p.Arg720Gln) c.*1897G>A (n.*1897G>A) c.489G>A c.238G>A c.1994G>A (p.Arg665Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.68695802G>C | CA396456210 | CDH3 | c.2159G>C (p.Arg720Pro) c.*1897G>C (n.*1897G>C) c.489G>C c.238G>C c.1994G>C (p.Arg665Pro) | |
16 | g.68695802G= | CA2229920435 | CDH3 | c.2159G= (p.Arg720=) c.*1897G= (n.*1897G=) c.489G= c.238G= c.1994G= (p.Arg665=) | |
16 | g.68695802G>T | CA396456209 | CDH3 | c.2159G>T (p.Arg720Leu) c.*1897G>T (n.*1897G>T) c.489G>T c.238G>T c.1994G>T (p.Arg665Leu) | |
16 | g.68695802dup | CA2633928559 | CDH3 | c.2159dup (p.Gly721ArgfsTer13) c.*1897dup (n.*1897dup) c.489dup c.238dup c.1994dup (p.Gly666ArgfsTer13) | gnomAD v4 |
16 | g.68695803A>C | CA496157716 | CDH3 | c.2160A>C (p.Arg720=) c.*1898A>C (n.*1898A>C) c.490A>C c.239A>C c.1995A>C (p.Arg665=) | |
16 | g.68695803A>G | CA496157717 | CDH3 | c.2160A>G (p.Arg720=) c.*1898A>G (n.*1898A>G) c.490A>G c.239A>G c.1995A>G (p.Arg665=) | |
16 | g.68695803A>T | CA496157718 | CDH3 | c.2160A>T (p.Arg720=) c.*1898A>T (n.*1898A>T) c.490A>T c.239A>T c.1995A>T (p.Arg665=) | |
16 | g.68695804G>A | CA396456211 | CDH3 | c.2161G>A (p.Gly721Ser) c.*1899G>A (n.*1899G>A) c.491G>A c.240G>A c.1996G>A (p.Gly666Ser) | |
16 | g.68695804G>C | CA8129604 | CDH3 | c.2161G>C (p.Gly721Arg) c.*1899G>C (n.*1899G>C) c.491G>C c.240G>C c.1996G>C (p.Gly666Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.68695804G= | CA2229920438 | CDH3 | c.2161G= (p.Gly721=) c.*1899G= (n.*1899G=) c.491G= c.240G= c.1996G= (p.Gly666=) | |
16 | g.68695804G>T | CA396456212 | CDH3 | c.2161G>T (p.Gly721Cys) c.*1899G>T (n.*1899G>T) c.491G>T c.240G>T c.1996G>T (p.Gly666Cys) | |
16 | g.68695805G>A | CA396456213 | CDH3 | c.2162G>A (p.Gly721Asp) c.*1900G>A (n.*1900G>A) c.492G>A c.241G>A c.1997G>A (p.Gly666Asp) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.68695805G>C | CA396456215 | CDH3 | c.2162G>C (p.Gly721Ala) c.*1900G>C (n.*1900G>C) c.492G>C c.241G>C c.1997G>C (p.Gly666Ala) | |
16 | g.68695805G= | CA2229920440 | CDH3 | c.2162G= (p.Gly721=) c.*1900G= (n.*1900G=) c.492G= c.241G= c.1997G= (p.Gly666=) | |
16 | g.68695805G>T | CA396456214 | CDH3 | c.2162G>T (p.Gly721Val) c.*1900G>T (n.*1900G>T) c.492G>T c.241G>T c.1997G>T (p.Gly666Val) | |
16 | g.68695805_68695806insCCTGGAC | CA2633928589 | CDH3 | c.2162_2163insCCTGGAC (p.Glu723AspfsTer13) c.*1900_*1901insCCTGGAC (n.*1900_*1901insCCTGGAC) c.492_493insCCTGGAC c.241_242insCCTGGAC c.1997_1998insCCTGGAC (p.Glu668AspfsTer13) | gnomAD v4 |
16 | g.68695806T>A | CA496157784 | CDH3 | c.2163T>A (p.Gly721=) c.*1901T>A (n.*1901T>A) c.493T>A c.242T>A c.1998T>A (p.Gly666=) | |
16 | g.68695806T>C | CA8129605 | CDH3 | c.2163T>C (p.Gly721=) c.*1901T>C (n.*1901T>C) c.493T>C c.242T>C c.1998T>C (p.Gly666=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695806T>G | CA496157786 | CDH3 | c.2163T>G (p.Gly721=) c.*1901T>G (n.*1901T>G) c.493T>G c.242T>G c.1998T>G (p.Gly666=) | |
16 | g.68695806T= | CA2229920442 | CDH3 | c.2163T= (p.Gly721=) c.*1901T= (n.*1901T=) c.493T= c.242T= c.1998T= (p.Gly666=) | |
16 | g.68695807C>A | CA396456216 | CDH3 | c.2164C>A (p.Leu722Met) c.*1902C>A (n.*1902C>A) c.494C>A c.243C>A c.1999C>A (p.Leu667Met) | gnomAD v4 |
16 | g.68695807C= | CA2229920445 | CDH3 | c.2164C= (p.Leu722=) c.*1902C= (n.*1902C=) c.494C= c.243C= c.1999C= (p.Leu667=) | |
16 | g.68695807C>G | CA396456217 | CDH3 | c.2164C>G (p.Leu722Val) c.*1902C>G (n.*1902C>G) c.494C>G c.243C>G c.1999C>G (p.Leu667Val) | |
16 | g.68695807C>T | CA8129606 | CDH3 | c.2164C>T (p.Leu722=) c.*1902C>T (n.*1902C>T) c.494C>T c.243C>T c.1999C>T (p.Leu667=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695808T>A | CA396456218 | CDH3 | c.2165T>A (p.Leu722Gln) c.*1903T>A (n.*1903T>A) c.495T>A c.244T>A c.2000T>A (p.Leu667Gln) | |
16 | g.68695808T>C | CA396456219 | CDH3 | c.2165T>C (p.Leu722Pro) c.*1903T>C (n.*1903T>C) c.495T>C c.244T>C c.2000T>C (p.Leu667Pro) | ClinVar |
16 | g.68695808T>G | CA396456220 | CDH3 | c.2165T>G (p.Leu722Arg) c.*1903T>G (n.*1903T>G) c.495T>G c.244T>G c.2000T>G (p.Leu667Arg) | |
16 | g.68695809G>A | CA496157794 | CDH3 | c.2166G>A (p.Leu722=) c.*1904G>A (n.*1904G>A) c.496G>A c.245G>A c.2001G>A (p.Leu667=) | |
16 | g.68695809G>C | CA496157796 | CDH3 | c.2166G>C (p.Leu722=) c.*1904G>C (n.*1904G>C) c.496G>C c.245G>C c.2001G>C (p.Leu667=) | |
16 | g.68695809G>T | CA496157797 | CDH3 | c.2166G>T (p.Leu722=) c.*1904G>T (n.*1904G>T) c.496G>T c.245G>T c.2001G>T (p.Leu667=) | |
16 | g.68695810G>A | CA396456221 | CDH3 | c.2167G>A (p.Glu723Lys) c.*1905G>A (n.*1905G>A) c.497G>A c.246G>A c.2002G>A (p.Glu668Lys) | |
16 | g.68695810G>C | CA396456222 | CDH3 | c.2167G>C (p.Glu723Gln) c.*1905G>C (n.*1905G>C) c.497G>C c.246G>C c.2002G>C (p.Glu668Gln) | |
16 | g.68695810G>T | CA396456223 | CDH3 | c.2167G>T (p.Glu723Ter) c.*1905G>T (n.*1905G>T) c.497G>T c.246G>T c.2002G>T (p.Glu668Ter) | |
16 | g.68695811A>C | CA396456226 | CDH3 | c.2168A>C (p.Glu723Ala) c.*1906A>C (n.*1906A>C) c.498A>C c.247A>C c.2003A>C (p.Glu668Ala) | |
16 | g.68695811A>G | CA396456225 | CDH3 | c.2168A>G (p.Glu723Gly) c.*1906A>G (n.*1906A>G) c.498A>G c.247A>G c.2003A>G (p.Glu668Gly) | |
16 | g.68695811A>T | CA396456224 | CDH3 | c.2168A>T (p.Glu723Val) c.*1906A>T (n.*1906A>T) c.498A>T c.247A>T c.2003A>T (p.Glu668Val) | |
16 | g.68695812G>A | CA8129607 | CDH3 | c.2169G>A (p.Glu723=) c.*1907G>A (n.*1907G>A) c.499G>A c.248G>A c.2004G>A (p.Glu668=) | dbSNP ExAC gnomAD v2 |
16 | g.68695812G>C | CA396456227 | CDH3 | c.2169G>C (p.Glu723Asp) c.*1907G>C (n.*1907G>C) c.499G>C c.248G>C c.2004G>C (p.Glu668Asp) | |
16 | g.68695812G= | CA2229920447 | CDH3 | c.2169G= (p.Glu723=) c.*1907G= (n.*1907G=) c.499G= c.248G= c.2004G= (p.Glu668=) | |
16 | g.68695812G>T | CA396456228 | CDH3 | c.2169G>T (p.Glu723Asp) c.*1907G>T (n.*1907G>T) c.499G>T c.248G>T c.2004G>T (p.Glu668Asp) | gnomAD v4 COSMIC COSMIC |
16 | g.68695813G>A | CA396456229 | CDH3 | c.2170G>A (p.Ala724Thr) c.*1908G>A (n.*1908G>A) c.500G>A c.249G>A c.2005G>A (p.Ala669Thr) | |
16 | g.68695813G>C | CA396456230 | CDH3 | c.2170G>C (p.Ala724Pro) c.*1908G>C (n.*1908G>C) c.500G>C c.249G>C c.2005G>C (p.Ala669Pro) | |
16 | g.68695813G= | CA2229920450 | CDH3 | c.2170G= (p.Ala724=) c.*1908G= (n.*1908G=) c.500G= c.249G= c.2005G= (p.Ala669=) | |
16 | g.68695813G>T | CA8129608 | CDH3 | c.2170G>T (p.Ala724Ser) c.*1908G>T (n.*1908G>T) c.500G>T c.249G>T c.2005G>T (p.Ala669Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695814C>A | CA396456231 | CDH3 | c.2171C>A (p.Ala724Asp) c.*1909C>A (n.*1909C>A) c.501C>A c.250C>A c.2006C>A (p.Ala669Asp) | |
16 | g.68695814C>G | CA396456232 | CDH3 | c.2171C>G (p.Ala724Gly) c.*1909C>G (n.*1909C>G) c.501C>G c.250C>G c.2006C>G (p.Ala669Gly) | gnomAD v4 |
16 | g.68695814C>T | CA396456233 | CDH3 | c.2171C>T (p.Ala724Val) c.*1909C>T (n.*1909C>T) c.501C>T c.250C>T c.2006C>T (p.Ala669Val) | |
16 | g.68695815C>A | CA496157812 | CDH3 | c.2172C>A (p.Ala724=) c.*1910C>A (n.*1910C>A) c.502C>A c.251C>A c.2007C>A (p.Ala669=) | |
16 | g.68695815C= | CA2229920455 | CDH3 | c.2172C= (p.Ala724=) c.*1910C= (n.*1910C=) c.502C= c.251C= c.2007C= (p.Ala669=) | |
16 | g.68695815C>G | CA496157813 | CDH3 | c.2172C>G (p.Ala724=) c.*1910C>G (n.*1910C>G) c.502C>G c.251C>G c.2007C>G (p.Ala669=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695815C>T | CA496157815 | CDH3 | c.2172C>T (p.Ala724=) c.*1910C>T (n.*1910C>T) c.502C>T c.251C>T c.2007C>T (p.Ala669=) | dbSNP |
16 | g.68695816A>C | CA496157817 | CDH3 | c.2173A>C (p.Arg725=) c.*1911A>C (n.*1911A>C) c.503A>C c.252A>C c.2008A>C (p.Arg670=) | |
16 | g.68695816A>G | CA396456234 | CDH3 | c.2173A>G (p.Arg725Gly) c.*1911A>G (n.*1911A>G) c.503A>G c.252A>G c.2008A>G (p.Arg670Gly) | |
16 | g.68695816A>T | CA396456235 | CDH3 | c.2173A>T (p.Arg725Trp) c.*1911A>T (n.*1911A>T) c.503A>T c.252A>T c.2008A>T (p.Arg670Trp) | |
16 | g.68695817G>A | CA8129609 | CDH3 | c.2174G>A (p.Arg725Lys) c.*1912G>A (n.*1912G>A) c.504G>A c.253G>A c.2009G>A (p.Arg670Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695817G>C | CA396456237 | CDH3 | c.2174G>C (p.Arg725Thr) c.*1912G>C (n.*1912G>C) c.504G>C c.253G>C c.2009G>C (p.Arg670Thr) | |
16 | g.68695817G= | CA2229920460 | CDH3 | c.2174G= (p.Arg725=) c.*1912G= (n.*1912G=) c.504G= c.253G= c.2009G= (p.Arg670=) | |
16 | g.68695817G>T | CA396456236 | CDH3 | c.2174G>T (p.Arg725Met) c.*1912G>T (n.*1912G>T) c.504G>T c.253G>T c.2009G>T (p.Arg670Met) | |
16 | g.68695818G>A | CA496157823 | CDH3 | c.2175G>A (p.Arg725=) c.*1913G>A (n.*1913G>A) c.505G>A c.254G>A c.2010G>A (p.Arg670=) | |
16 | g.68695818G>C | CA396456238 | CDH3 | c.2175G>C (p.Arg725Ser) c.*1913G>C (n.*1913G>C) c.505G>C c.254G>C c.2010G>C (p.Arg670Ser) | |
16 | g.68695818G>T | CA396456239 | CDH3 | c.2175G>T (p.Arg725Ser) c.*1913G>T (n.*1913G>T) c.505G>T c.254G>T c.2010G>T (p.Arg670Ser) | |
16 | g.68695819C>A | CA396456240 | CDH3 | c.2176C>A (p.Pro726Thr) c.*1914C>A (n.*1914C>A) c.506C>A c.255C>A c.2011C>A (p.Pro671Thr) | |
16 | g.68695819C>G | CA396456241 | CDH3 | c.2176C>G (p.Pro726Ala) c.*1914C>G (n.*1914C>G) c.506C>G c.255C>G c.2011C>G (p.Pro671Ala) | |
16 | g.68695819C>T | CA396456242 | CDH3 | c.2176C>T (p.Pro726Ser) c.*1914C>T (n.*1914C>T) c.506C>T c.255C>T c.2011C>T (p.Pro671Ser) | |
16 | g.68695820C>A | CA396456243 | CDH3 | c.2177C>A (p.Pro726Gln) c.*1915C>A (n.*1915C>A) c.507C>A c.256C>A c.2012C>A (p.Pro671Gln) | |
16 | g.68695820C= | CA2229920462 | CDH3 | c.2177C= (p.Pro726=) c.*1915C= (n.*1915C=) c.507C= c.256C= c.2012C= (p.Pro671=) | |
16 | g.68695820C>G | CA396456244 | CDH3 | c.2177C>G (p.Pro726Arg) c.*1915C>G (n.*1915C>G) c.507C>G c.256C>G c.2012C>G (p.Pro671Arg) | |
16 | g.68695820C>T | CA8129610 | CDH3 | c.2177C>T (p.Pro726Leu) c.*1915C>T (n.*1915C>T) c.507C>T c.256C>T c.2012C>T (p.Pro671Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695821G>A | CA221737 | CDH3 | c.2178G>A (p.Pro726=) c.*1916G>A (n.*1916G>A) c.508G>A c.257G>A c.2013G>A (p.Pro671=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.68695821G>C | CA283289461 | CDH3 | c.2178G>C (p.Pro726=) c.*1916G>C (n.*1916G>C) c.508G>C c.257G>C c.2013G>C (p.Pro671=) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.68695821G= | CA2229920469 | CDH3 | c.2178G= (p.Pro726=) c.*1916G= (n.*1916G=) c.508G= c.257G= c.2013G= (p.Pro671=) | |
16 | g.68695821G>T | CA496157839 | CDH3 | c.2178G>T (p.Pro726=) c.*1916G>T (n.*1916G>T) c.508G>T c.257G>T c.2013G>T (p.Pro671=) | |
16 | g.68695822G>A | CA8129611 | CDH3 | c.2179G>A (p.Glu727Lys) c.*1917G>A (n.*1917G>A) c.509G>A c.258G>A c.2014G>A (p.Glu672Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695822G>C | CA396456245 | CDH3 | c.2179G>C (p.Glu727Gln) c.*1917G>C (n.*1917G>C) c.509G>C c.258G>C c.2014G>C (p.Glu672Gln) | |
16 | g.68695822G= | CA2229920473 | CDH3 | c.2179G= (p.Glu727=) c.*1917G= (n.*1917G=) c.509G= c.258G= c.2014G= (p.Glu672=) | |
16 | g.68695822G>T | CA396456246 | CDH3 | c.2179G>T (p.Glu727Ter) c.*1917G>T (n.*1917G>T) c.509G>T c.258G>T c.2014G>T (p.Glu672Ter) | |
16 | g.68695823A>C | CA396456249 | CDH3 | c.2180A>C (p.Glu727Ala) c.*1918A>C (n.*1918A>C) c.510A>C c.259A>C c.2015A>C (p.Glu672Ala) | |
16 | g.68695823A>G | CA396456247 | CDH3 | c.2180A>G (p.Glu727Gly) c.*1918A>G (n.*1918A>G) c.510A>G c.259A>G c.2015A>G (p.Glu672Gly) | |
16 | g.68695823A>T | CA396456248 | CDH3 | c.2180A>T (p.Glu727Val) c.*1918A>T (n.*1918A>T) c.510A>T c.259A>T c.2015A>T (p.Glu672Val) | |
16 | g.68695824G>A | CA496157847 | CDH3 | c.2181G>A (p.Glu727=) c.*1919G>A (n.*1919G>A) c.511G>A c.260G>A c.2016G>A (p.Glu672=) | |
16 | g.68695824G>C | CA396456250 | CDH3 | c.2181G>C (p.Glu727Asp) c.*1919G>C (n.*1919G>C) c.511G>C c.260G>C c.2016G>C (p.Glu672Asp) | |
16 | g.68695824G>T | CA396456251 | CDH3 | c.2181G>T (p.Glu727Asp) c.*1919G>T (n.*1919G>T) c.511G>T c.260G>T c.2016G>T (p.Glu672Asp) | |
16 | g.68695825G>A | CA396456252 | CDH3 | c.2182G>A (p.Val728Met) c.1G>A (p.Val1Met) c.*1920G>A (n.*1920G>A) c.512G>A c.261G>A c.2017G>A (p.Val673Met) | |
16 | g.68695825G>C | CA396456253 | CDH3 | c.2182G>C (p.Val728Leu) c.1G>C (p.Val1Leu) c.*1920G>C (n.*1920G>C) c.512G>C c.261G>C c.2017G>C (p.Val673Leu) | |
16 | g.68695825G>T | CA396456254 | CDH3 | c.2182G>T (p.Val728Leu) c.1G>T (p.Val1Leu) c.*1920G>T (n.*1920G>T) c.512G>T c.261G>T c.2017G>T (p.Val673Leu) | |
16 | g.68695826T>A | CA396456255 | CDH3 | c.2183T>A (p.Val728Glu) c.2T>A (p.Val1Glu) c.*1921T>A (n.*1921T>A) c.513T>A c.262T>A c.2018T>A (p.Val673Glu) | |
16 | g.68695826T>C | CA396456256 | CDH3 | c.2183T>C (p.Val728Ala) c.2T>C (p.Val1Ala) c.*1921T>C (n.*1921T>C) c.513T>C c.262T>C c.2018T>C (p.Val673Ala) | |
16 | g.68695826T>G | CA396456257 | CDH3 | c.2183T>G (p.Val728Gly) c.2T>G (p.Val1Gly) c.*1921T>G (n.*1921T>G) c.513T>G c.262T>G c.2018T>G (p.Val673Gly) | |
16 | g.68695827G>A | CA496157863 | CDH3 | c.2184G>A (p.Val728=) c.3G>A (p.Val1=) c.*1922G>A (n.*1922G>A) c.514G>A c.263G>A c.2019G>A (p.Val673=) | |
16 | g.68695827G>C | CA496157861 | CDH3 | c.2184G>C (p.Val728=) c.3G>C (p.Val1=) c.*1922G>C (n.*1922G>C) c.514G>C c.263G>C c.2019G>C (p.Val673=) | gnomAD v4 |
16 | g.68695827G>T | CA496157859 | CDH3 | c.2184G>T (p.Val728=) c.3G>T (p.Val1=) c.*1922G>T (n.*1922G>T) c.514G>T c.263G>T c.2019G>T (p.Val673=) | |
16 | g.68695828G>A | CA396456258 | CDH3 | c.2185G>A (p.Val729Ile) c.4G>A (p.Val2Ile) c.*1923G>A (n.*1923G>A) c.515G>A c.264G>A c.2020G>A (p.Val674Ile) | |
16 | g.68695828G>C | CA396456259 | CDH3 | c.2185G>C (p.Val729Leu) c.4G>C (p.Val2Leu) c.*1923G>C (n.*1923G>C) c.515G>C c.264G>C c.2020G>C (p.Val674Leu) | dbSNP |
16 | g.68695828G>T | CA396456260 | CDH3 | c.2185G>T (p.Val729Phe) c.4G>T (p.Val2Phe) c.*1923G>T (n.*1923G>T) c.515G>T c.264G>T c.2020G>T (p.Val674Phe) | |
16 | g.68695829T>A | CA396456262 | CDH3 | c.2186T>A (p.Val729Asp) c.5T>A (p.Val2Asp) c.*1924T>A (n.*1924T>A) c.516T>A c.265T>A c.2021T>A (p.Val674Asp) | dbSNP |
16 | g.68695829T>C | CA396456263 | CDH3 | c.2186T>C (p.Val729Ala) c.5T>C (p.Val2Ala) c.*1924T>C (n.*1924T>C) c.516T>C c.265T>C c.2021T>C (p.Val674Ala) | |
16 | g.68695829T>G | CA396456261 | CDH3 | c.2186T>G (p.Val729Gly) c.5T>G (p.Val2Gly) c.*1924T>G (n.*1924T>G) c.516T>G c.265T>G c.2021T>G (p.Val674Gly) | |
16 | g.68695830T>A | CA496157871 | CDH3 | c.2187T>A (p.Val729=) c.6T>A (p.Val2=) c.*1925T>A (n.*1925T>A) c.517T>A c.266T>A c.2022T>A (p.Val674=) | |
16 | g.68695830T>C | CA496157873 | CDH3 | c.2187T>C (p.Val729=) c.6T>C (p.Val2=) c.*1925T>C (n.*1925T>C) c.517T>C c.266T>C c.2022T>C (p.Val674=) | |
16 | g.68695830T>G | CA496157874 | CDH3 | c.2187T>G (p.Val729=) c.6T>G (p.Val2=) c.*1925T>G (n.*1925T>G) c.517T>G c.266T>G c.2022T>G (p.Val674=) | |
16 | g.68695831C>A | CA396456266 | CDH3 | c.2188C>A (p.Leu730Ile) c.7C>A (p.Leu3Ile) c.*1926C>A (n.*1926C>A) c.518C>A c.267C>A c.2023C>A (p.Leu675Ile) | |
16 | g.68695831C>G | CA396456264 | CDH3 | c.2188C>G (p.Leu730Val) c.7C>G (p.Leu3Val) c.*1926C>G (n.*1926C>G) c.518C>G c.267C>G c.2023C>G (p.Leu675Val) | |
16 | g.68695831C>T | CA396456265 | CDH3 | c.2188C>T (p.Leu730Phe) c.7C>T (p.Leu3Phe) c.*1926C>T (n.*1926C>T) c.518C>T c.267C>T c.2023C>T (p.Leu675Phe) | |
16 | g.68695832T>A | CA396456267 | CDH3 | c.2189T>A (p.Leu730His) c.8T>A (p.Leu3His) c.*1927T>A (n.*1927T>A) c.519T>A c.268T>A c.2024T>A (p.Leu675His) | |
16 | g.68695832T>C | CA396456268 | CDH3 | c.2189T>C (p.Leu730Pro) c.8T>C (p.Leu3Pro) c.*1927T>C (n.*1927T>C) c.519T>C c.268T>C c.2024T>C (p.Leu675Pro) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.68695832T>G | CA396456269 | CDH3 | c.2189T>G (p.Leu730Arg) c.8T>G (p.Leu3Arg) c.*1927T>G (n.*1927T>G) c.519T>G c.268T>G c.2024T>G (p.Leu675Arg) | gnomAD v4 |
16 | g.68695832T= | CA2229920476 | CDH3 | c.2189T= (p.Leu730=) c.8T= (p.Leu3=) c.*1927T= (n.*1927T=) c.519T= c.268T= c.2024T= (p.Leu675=) | |
16 | g.68695833C>A | CA496157884 | CDH3 | c.2190C>A (p.Leu730=) c.9C>A (p.Leu3=) c.*1928C>A (n.*1928C>A) c.520C>A c.269C>A c.2025C>A (p.Leu675=) | |
16 | g.68695833C= | CA2229920479 | CDH3 | c.2190C= (p.Leu730=) c.9C= (p.Leu3=) c.*1928C= (n.*1928C=) c.520C= c.269C= c.2025C= (p.Leu675=) | |
16 | g.68695833C>G | CA283289463 | CDH3 | c.2190C>G (p.Leu730=) c.9C>G (p.Leu3=) c.*1928C>G (n.*1928C>G) c.520C>G c.269C>G c.2025C>G (p.Leu675=) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.68695833C>T | CA496157887 | CDH3 | c.2190C>T (p.Leu730=) c.9C>T (p.Leu3=) c.*1928C>T (n.*1928C>T) c.520C>T c.269C>T c.2025C>T (p.Leu675=) | ClinVar |
16 | g.68695834C>A | CA396456271 | CDH3 | c.2191C>A (p.Arg731Ser) c.10C>A (p.Arg4Ser) c.*1929C>A (n.*1929C>A) c.521C>A c.270C>A c.2026C>A (p.Arg676Ser) | gnomAD v4 |
16 | g.68695834C= | CA2229920484 | CDH3 | c.2191C= (p.Arg731=) c.10C= (p.Arg4=) c.*1929C= (n.*1929C=) c.521C= c.270C= c.2026C= (p.Arg676=) | |
16 | g.68695834C>G | CA396456270 | CDH3 | c.2191C>G (p.Arg731Gly) c.10C>G (p.Arg4Gly) c.*1929C>G (n.*1929C>G) c.521C>G c.270C>G c.2026C>G (p.Arg676Gly) | dbSNP |
16 | g.68695834C>T | CA8129612 | CDH3 | c.2191C>T (p.Arg731Cys) c.10C>T (p.Arg4Cys) c.*1929C>T (n.*1929C>T) c.521C>T c.270C>T c.2026C>T (p.Arg676Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695835G>A | CA8129613 | CDH3 | c.2192G>A (p.Arg731His) c.11G>A (p.Arg4His) c.*1930G>A (n.*1930G>A) c.522G>A c.271G>A c.2027G>A (p.Arg676His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
16 | g.68695835G>C | CA396456272 | CDH3 | c.2192G>C (p.Arg731Pro) c.11G>C (p.Arg4Pro) c.*1930G>C (n.*1930G>C) c.522G>C c.271G>C c.2027G>C (p.Arg676Pro) | |
16 | g.68695835G= | CA2229920488 | CDH3 | c.2192G= (p.Arg731=) c.11G= (p.Arg4=) c.*1930G= (n.*1930G=) c.522G= c.271G= c.2027G= (p.Arg676=) | |
16 | g.68695835G>T | CA283289476 | CDH3 | c.2192G>T (p.Arg731Leu) c.11G>T (p.Arg4Leu) c.*1930G>T (n.*1930G>T) c.522G>T c.271G>T c.2027G>T (p.Arg676Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695836C>A | CA496157896 | CDH3 | c.2193C>A (p.Arg731=) c.12C>A (p.Arg4=) c.*1931C>A (n.*1931C>A) c.523C>A c.272C>A c.2028C>A (p.Arg676=) | |
16 | g.68695836C= | CA2229920491 | CDH3 | c.2193C= (p.Arg731=) c.12C= (p.Arg4=) c.*1931C= (n.*1931C=) c.523C= c.272C= c.2028C= (p.Arg676=) | |
16 | g.68695836C>G | CA496157898 | CDH3 | c.2193C>G (p.Arg731=) c.12C>G (p.Arg4=) c.*1931C>G (n.*1931C>G) c.523C>G c.272C>G c.2028C>G (p.Arg676=) | |
16 | g.68695836C>T | CA496157900 | CDH3 | c.2193C>T (p.Arg731=) c.12C>T (p.Arg4=) c.*1931C>T (n.*1931C>T) c.523C>T c.272C>T c.2028C>T (p.Arg676=) | ClinVar dbSNP |
16 | g.68695837A>C | CA396456273 | CDH3 | c.2194A>C (p.Asn732His) c.13A>C (p.Asn5His) c.*1932A>C (n.*1932A>C) c.524A>C c.273A>C c.2029A>C (p.Asn677His) | gnomAD v4 |
16 | g.68695837A>G | CA396456274 | CDH3 | c.2194A>G (p.Asn732Asp) c.13A>G (p.Asn5Asp) c.*1932A>G (n.*1932A>G) c.524A>G c.273A>G c.2029A>G (p.Asn677Asp) | |
16 | g.68695837A>T | CA396456275 | CDH3 | c.2194A>T (p.Asn732Tyr) c.13A>T (p.Asn5Tyr) c.*1932A>T (n.*1932A>T) c.524A>T c.273A>T c.2029A>T (p.Asn677Tyr) | |
16 | g.68695838A>C | CA396456276 | CDH3 | c.2195A>C (p.Asn732Thr) c.14A>C (p.Asn5Thr) c.*1933A>C (n.*1933A>C) c.525A>C c.274A>C c.2030A>C (p.Asn677Thr) | |
16 | g.68695838A>G | CA396456278 | CDH3 | c.2195A>G (p.Asn732Ser) c.14A>G (p.Asn5Ser) c.*1933A>G (n.*1933A>G) c.525A>G c.274A>G c.2030A>G (p.Asn677Ser) | gnomAD v4 |
16 | g.68695838A>T | CA396456277 | CDH3 | c.2195A>T (p.Asn732Ile) c.14A>T (p.Asn5Ile) c.*1933A>T (n.*1933A>T) c.525A>T c.274A>T c.2030A>T (p.Asn677Ile) | |
16 | g.68695839T>A | CA396456279 | CDH3 | c.2196T>A (p.Asn732Lys) c.15T>A (p.Asn5Lys) c.*1934T>A (n.*1934T>A) c.526T>A c.275T>A c.2031T>A (p.Asn677Lys) | |
16 | g.68695839T>C | CA496157910 | CDH3 | c.2196T>C (p.Asn732=) c.15T>C (p.Asn5=) c.*1934T>C (n.*1934T>C) c.526T>C c.275T>C c.2031T>C (p.Asn677=) | |
16 | g.68695839T>G | CA8129614 | CDH3 | c.2196T>G (p.Asn732Lys) c.15T>G (p.Asn5Lys) c.*1934T>G (n.*1934T>G) c.526T>G c.275T>G c.2031T>G (p.Asn677Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.68695839T= | CA2229920493 | CDH3 | c.2196T= (p.Asn732=) c.15T= (p.Asn5=) c.*1934T= (n.*1934T=) c.526T= c.275T= c.2031T= (p.Asn677=) | |
16 | g.68695840G>A | CA396456280 | CDH3 | c.2197G>A (p.Asp733Asn) c.16G>A (p.Asp6Asn) c.*1935G>A (n.*1935G>A) c.527G>A c.276G>A c.2032G>A (p.Asp678Asn) | gnomAD v4 |
16 | g.68695840G>C | CA396456281 | CDH3 | c.2197G>C (p.Asp733His) c.16G>C (p.Asp6His) c.*1935G>C (n.*1935G>C) c.527G>C c.276G>C c.2032G>C (p.Asp678His) | gnomAD v4 |
16 | g.68695840G>T | CA396456282 | CDH3 | c.2197G>T (p.Asp733Tyr) c.16G>T (p.Asp6Tyr) c.*1935G>T (n.*1935G>T) c.527G>T c.276G>T c.2032G>T (p.Asp678Tyr) | |
16 | g.68695841A>C | CA396456283 | CDH3 | c.2198A>C (p.Asp733Ala) c.17A>C (p.Asp6Ala) c.*1936A>C (n.*1936A>C) c.528A>C c.277A>C c.2033A>C (p.Asp678Ala) | |
16 | g.68695841A>G | CA396456284 | CDH3 | c.2198A>G (p.Asp733Gly) c.17A>G (p.Asp6Gly) c.*1936A>G (n.*1936A>G) c.528A>G c.277A>G c.2033A>G (p.Asp678Gly) | |
16 | g.68695841A>T | CA396456285 | CDH3 | c.2198A>T (p.Asp733Val) c.17A>T (p.Asp6Val) c.*1936A>T (n.*1936A>T) c.528A>T c.277A>T c.2033A>T (p.Asp678Val) | |
16 | g.68695842C>A | CA396456286 | CDH3 | c.2199C>A (p.Asp733Glu) c.18C>A (p.Asp6Glu) c.*1937C>A (n.*1937C>A) c.529C>A c.278C>A c.2034C>A (p.Asp678Glu) | |
16 | g.68695842C= | CA2229920495 | CDH3 | c.2199C= (p.Asp733=) c.18C= (p.Asp6=) c.*1937C= (n.*1937C=) c.529C= c.278C= c.2034C= (p.Asp678=) | |
16 | g.68695842C>G | CA396456287 | CDH3 | c.2199C>G (p.Asp733Glu) c.18C>G (p.Asp6Glu) c.*1937C>G (n.*1937C>G) c.529C>G c.278C>G c.2034C>G (p.Asp678Glu) | gnomAD v4 |
16 | g.68695842C>T | CA8129615 | CDH3 | c.2199C>T (p.Asp733=) c.18C>T (p.Asp6=) c.*1937C>T (n.*1937C>T) c.529C>T c.278C>T c.2034C>T (p.Asp678=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695843G>A | CA8129616 | CDH3 | c.2200G>A (p.Val734Met) c.19G>A (p.Val7Met) c.*1938G>A (n.*1938G>A) c.530G>A c.279G>A c.2035G>A (p.Val679Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695843G>C | CA8129617 | CDH3 | c.2200G>C (p.Val734Leu) c.19G>C (p.Val7Leu) c.*1938G>C (n.*1938G>C) c.530G>C c.279G>C c.2035G>C (p.Val679Leu) | dbSNP ExAC gnomAD v2 |
16 | g.68695843G= | CA2229920499 | CDH3 | c.2200G= (p.Val734=) c.19G= (p.Val7=) c.*1938G= (n.*1938G=) c.530G= c.279G= c.2035G= (p.Val679=) | |
16 | g.68695843G>T | CA8129618 | CDH3 | c.2200G>T (p.Val734Leu) c.19G>T (p.Val7Leu) c.*1938G>T (n.*1938G>T) c.530G>T c.279G>T c.2035G>T (p.Val679Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.68695844T>A | CA396456288 | CDH3 | c.2201T>A (p.Val734Glu) c.20T>A (p.Val7Glu) c.*1939T>A (n.*1939T>A) c.531T>A c.280T>A c.2036T>A (p.Val679Glu) | |
16 | g.68695844T>C | CA396456289 | CDH3 | c.2201T>C (p.Val734Ala) c.20T>C (p.Val7Ala) c.*1939T>C (n.*1939T>C) c.531T>C c.280T>C c.2036T>C (p.Val679Ala) | |
16 | g.68695844T>G | CA396456290 | CDH3 | c.2201T>G (p.Val734Gly) c.20T>G (p.Val7Gly) c.*1939T>G (n.*1939T>G) c.531T>G c.280T>G c.2036T>G (p.Val679Gly) | |
16 | g.68695845G>A | CA8129619 | CDH3 | c.2202G>A (p.Val734=) c.21G>A (p.Val7=) c.*1940G>A (n.*1940G>A) c.532G>A c.281G>A c.2037G>A (p.Val679=) | dbSNP ExAC gnomAD v2 |
16 | g.68695845G>C | CA496157938 | CDH3 | c.2202G>C (p.Val734=) c.21G>C (p.Val7=) c.*1940G>C (n.*1940G>C) c.532G>C c.281G>C c.2037G>C (p.Val679=) | |
16 | g.68695845G= | CA2229920506 | CDH3 | c.2202G= (p.Val734=) c.21G= (p.Val7=) c.*1940G= (n.*1940G=) c.532G= c.281G= c.2037G= (p.Val679=) | |
16 | g.68695845G>T | CA496157942 | CDH3 | c.2202G>T (p.Val734=) c.21G>T (p.Val7=) c.*1940G>T (n.*1940G>T) c.532G>T c.281G>T c.2037G>T (p.Val679=) | |
16 | g.68695846G>A | CA396456291 | CDH3 | c.2203G>A (p.Ala735Thr) c.22G>A (p.Ala8Thr) c.*1941G>A (n.*1941G>A) c.533G>A c.282G>A c.2038G>A (p.Ala680Thr) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.68695846G>C | CA396456292 | CDH3 | c.2203G>C (p.Ala735Pro) c.22G>C (p.Ala8Pro) c.*1941G>C (n.*1941G>C) c.533G>C c.282G>C c.2038G>C (p.Ala680Pro) | |
16 | g.68695846G= | CA2229920508 | CDH3 | c.2203G= (p.Ala735=) c.22G= (p.Ala8=) c.*1941G= (n.*1941G=) c.533G= c.282G= c.2038G= (p.Ala680=) | |
16 | g.68695846G>T | CA396456293 | CDH3 | c.2203G>T (p.Ala735Ser) c.22G>T (p.Ala8Ser) c.*1941G>T (n.*1941G>T) c.533G>T c.282G>T c.2038G>T (p.Ala680Ser) | |
16 | g.68695847C>A | CA396456294 | CDH3 | c.2204C>A (p.Ala735Glu) c.23C>A (p.Ala8Glu) c.*1942C>A (n.*1942C>A) c.534C>A c.283C>A c.2039C>A (p.Ala680Glu) | |
16 | g.68695847C= | CA2229920511 | CDH3 | c.2204C= (p.Ala735=) c.23C= (p.Ala8=) c.*1942C= (n.*1942C=) c.534C= c.283C= c.2039C= (p.Ala680=) | |
16 | g.68695847C>G | CA396456295 | CDH3 | c.2204C>G (p.Ala735Gly) c.23C>G (p.Ala8Gly) c.*1942C>G (n.*1942C>G) c.534C>G c.283C>G c.2039C>G (p.Ala680Gly) | |
16 | g.68695847C>T | CA396456296 | CDH3 | c.2204C>T (p.Ala735Val) c.23C>T (p.Ala8Val) c.*1942C>T (n.*1942C>T) c.534C>T c.283C>T c.2039C>T (p.Ala680Val) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.68695848A= | CA2229920513 | CDH3 | c.2205A= (p.Ala735=) c.24A= (p.Ala8=) c.*1943A= (n.*1943A=) c.535A= c.284A= c.2040A= (p.Ala680=) | |
16 | g.68695848A>C | CA496157949 | CDH3 | c.2205A>C (p.Ala735=) c.24A>C (p.Ala8=) c.*1943A>C (n.*1943A>C) c.535A>C c.284A>C c.2040A>C (p.Ala680=) | |
16 | g.68695848A>G | CA496157952 | CDH3 | c.2205A>G (p.Ala735=) c.24A>G (p.Ala8=) c.*1943A>G (n.*1943A>G) c.535A>G c.284A>G c.2040A>G (p.Ala680=) | dbSNP gnomAD v4 |
16 | g.68695848A>T | CA496157951 | CDH3 | c.2205A>T (p.Ala735=) c.24A>T (p.Ala8=) c.*1943A>T (n.*1943A>T) c.535A>T c.284A>T c.2040A>T (p.Ala680=) | |
16 | g.68695849C>A | CA396456297 | CDH3 | c.2206C>A (p.Pro736Thr) c.25C>A (p.Pro9Thr) c.*1944C>A (n.*1944C>A) c.536C>A c.285C>A c.2041C>A (p.Pro681Thr) | |
16 | g.68695849C>G | CA396456298 | CDH3 | c.2206C>G (p.Pro736Ala) c.25C>G (p.Pro9Ala) c.*1944C>G (n.*1944C>G) c.536C>G c.285C>G c.2041C>G (p.Pro681Ala) | |
16 | g.68695849C>T | CA396456299 | CDH3 | c.2206C>T (p.Pro736Ser) c.25C>T (p.Pro9Ser) c.*1944C>T (n.*1944C>T) c.536C>T c.285C>T c.2041C>T (p.Pro681Ser) | |
16 | g.68695850C>A | CA396456302 | CDH3 | c.2207C>A (p.Pro736Gln) c.26C>A (p.Pro9Gln) c.*1945C>A (n.*1945C>A) c.537C>A c.286C>A c.2042C>A (p.Pro681Gln) | |
16 | g.68695850C>G | CA396456300 | CDH3 | c.2207C>G (p.Pro736Arg) c.26C>G (p.Pro9Arg) c.*1945C>G (n.*1945C>G) c.537C>G c.286C>G c.2042C>G (p.Pro681Arg) | |
16 | g.68695850C>T | CA396456301 | CDH3 | c.2207C>T (p.Pro736Leu) c.26C>T (p.Pro9Leu) c.*1945C>T (n.*1945C>T) c.537C>T c.286C>T c.2042C>T (p.Pro681Leu) | gnomAD v4 |
16 | g.68695851A>C | CA496157961 | CDH3 | c.2208A>C (p.Pro736=) c.27A>C (p.Pro9=) c.*1946A>C (n.*1946A>C) c.538A>C c.287A>C c.2043A>C (p.Pro681=) | |
16 | g.68695851A>G | CA496157963 | CDH3 | c.2208A>G (p.Pro736=) c.27A>G (p.Pro9=) c.*1946A>G (n.*1946A>G) c.538A>G c.287A>G c.2043A>G (p.Pro681=) | |
16 | g.68695851A>T | CA496157965 | CDH3 | c.2208A>T (p.Pro736=) c.27A>T (p.Pro9=) c.*1946A>T (n.*1946A>T) c.538A>T c.287A>T c.2043A>T (p.Pro681=) | |
16 | g.68695852A= | CA2229920517 | CDH3 | c.2209A= (p.Thr737=) c.28A= (p.Thr10=) c.*1947A= (n.*1947A=) c.539A= c.288A= c.2044A= (p.Thr682=) | |
16 | g.68695852A>C | CA396456303 | CDH3 | c.2209A>C (p.Thr737Pro) c.28A>C (p.Thr10Pro) c.*1947A>C (n.*1947A>C) c.539A>C c.288A>C c.2044A>C (p.Thr682Pro) | |
16 | g.68695852A>G | CA8129620 | CDH3 | c.2209A>G (p.Thr737Ala) c.28A>G (p.Thr10Ala) c.*1947A>G (n.*1947A>G) c.539A>G c.288A>G c.2044A>G (p.Thr682Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
16 | g.68695852A>T | CA396456304 | CDH3 | c.2209A>T (p.Thr737Ser) c.28A>T (p.Thr10Ser) c.*1947A>T (n.*1947A>T) c.539A>T c.288A>T c.2044A>T (p.Thr682Ser) | gnomAD v4 |
16 | g.68695853C>A | CA396456305 | CDH3 | c.2210C>A (p.Thr737Asn) c.29C>A (p.Thr10Asn) c.*1948C>A (n.*1948C>A) c.540C>A c.289C>A c.2045C>A (p.Thr682Asn) | |
16 | g.68695853C>G | CA396456306 | CDH3 | c.2210C>G (p.Thr737Ser) c.29C>G (p.Thr10Ser) c.*1948C>G (n.*1948C>G) c.540C>G c.289C>G c.2045C>G (p.Thr682Ser) | |
16 | g.68695853C>T | CA396456307 | CDH3 | c.2210C>T (p.Thr737Ile) c.29C>T (p.Thr10Ile) c.*1948C>T (n.*1948C>T) c.540C>T c.289C>T c.2045C>T (p.Thr682Ile) | |
16 | g.68695854C>A | CA496157976 | CDH3 | c.2211C>A (p.Thr737=) c.30C>A (p.Thr10=) c.*1949C>A (n.*1949C>A) c.541C>A c.290C>A c.2046C>A (p.Thr682=) | |
16 | g.68695854C= | CA2229920520 | CDH3 | c.2211C= (p.Thr737=) c.30C= (p.Thr10=) c.*1949C= (n.*1949C=) c.541C= c.290C= c.2046C= (p.Thr682=) | |
16 | g.68695854C>G | CA496157977 | CDH3 | c.2211C>G (p.Thr737=) c.30C>G (p.Thr10=) c.*1949C>G (n.*1949C>G) c.541C>G c.290C>G c.2046C>G (p.Thr682=) | |
16 | g.68695854C>T | CA496157978 | CDH3 | c.2211C>T (p.Thr737=) c.30C>T (p.Thr10=) c.*1949C>T (n.*1949C>T) c.541C>T c.290C>T c.2046C>T (p.Thr682=) | ClinVar dbSNP gnomAD v4 |
16 | g.68695858_68695860dup | CA2633928708 | CDH3 | c.2215_2217dup (p.Ile739_Pro740insIle) c.34_36dup (p.Ile12_Pro13insIle) c.*1953_*1955dup (n.*1953_*1955dup) c.545_547dup c.294_296dup c.2050_2052dup (p.Ile684_Pro685insIle) | gnomAD v4 |
16 | g.68695855A>C | CA396456308 | CDH3 | c.2212A>C (p.Ile738Leu) c.31A>C (p.Ile11Leu) c.*1950A>C (n.*1950A>C) c.542A>C c.291A>C c.2047A>C (p.Ile683Leu) | |
16 | g.68695855A>G | CA396456309 | CDH3 | c.2212A>G (p.Ile738Val) c.31A>G (p.Ile11Val) c.*1950A>G (n.*1950A>G) c.542A>G c.291A>G c.2047A>G (p.Ile683Val) | |
16 | g.68695855A>T | CA396456310 | CDH3 | c.2212A>T (p.Ile738Phe) c.31A>T (p.Ile11Phe) c.*1950A>T (n.*1950A>T) c.542A>T c.291A>T c.2047A>T (p.Ile683Phe) | |
16 | g.68695856T>A | CA396456311 | CDH3 | c.2213T>A (p.Ile738Asn) c.32T>A (p.Ile11Asn) c.*1951T>A (n.*1951T>A) c.543T>A c.292T>A c.2048T>A (p.Ile683Asn) | |
16 | g.68695856T>C | CA396456312 | CDH3 | c.2213T>C (p.Ile738Thr) c.32T>C (p.Ile11Thr) c.*1951T>C (n.*1951T>C) c.543T>C c.292T>C c.2048T>C (p.Ile683Thr) | |
16 | g.68695856T>G | CA396456313 | CDH3 | c.2213T>G (p.Ile738Ser) c.32T>G (p.Ile11Ser) c.*1951T>G (n.*1951T>G) c.543T>G c.292T>G c.2048T>G (p.Ile683Ser) | |
16 | g.68695857C>A | CA496157980 | CDH3 | c.2214C>A (p.Ile738=) c.33C>A (p.Ile11=) c.*1952C>A (n.*1952C>A) c.544C>A c.293C>A c.2049C>A (p.Ile683=) | |
16 | g.68695857C>G | CA396456314 | CDH3 | c.2214C>G (p.Ile738Met) c.33C>G (p.Ile11Met) c.*1952C>G (n.*1952C>G) c.544C>G c.293C>G c.2049C>G (p.Ile683Met) | |
16 | g.68695857C>T | CA496157984 | CDH3 | c.2214C>T (p.Ile738=) c.33C>T (p.Ile11=) c.*1952C>T (n.*1952C>T) c.544C>T c.293C>T c.2049C>T (p.Ile683=) | |
16 | g.68695858A>C | CA396456316 | CDH3 | c.2215A>C (p.Ile739Leu) c.34A>C (p.Ile12Leu) c.*1953A>C (n.*1953A>C) c.545A>C c.294A>C c.2050A>C (p.Ile684Leu) | |
16 | g.68695858A>G | CA396456317 | CDH3 | c.2215A>G (p.Ile739Val) c.34A>G (p.Ile12Val) c.*1953A>G (n.*1953A>G) c.545A>G c.294A>G c.2050A>G (p.Ile684Val) | |
16 | g.68695858A>T | CA396456315 | CDH3 | c.2215A>T (p.Ile739Phe) c.34A>T (p.Ile12Phe) c.*1953A>T (n.*1953A>T) c.545A>T c.294A>T c.2050A>T (p.Ile684Phe) | ClinVar dbSNP |
16 | g.68695859T>A | CA396456319 | CDH3 | c.2216T>A (p.Ile739Asn) c.35T>A (p.Ile12Asn) c.*1954T>A (n.*1954T>A) c.546T>A c.295T>A c.2051T>A (p.Ile684Asn) | |
16 | g.68695859T>C | CA396456318 | CDH3 | c.2216T>C (p.Ile739Thr) c.35T>C (p.Ile12Thr) c.*1954T>C (n.*1954T>C) c.546T>C c.295T>C c.2051T>C (p.Ile684Thr) | |
16 | g.68695859T>G | CA396456320 | CDH3 | c.2216T>G (p.Ile739Ser) c.35T>G (p.Ile12Ser) c.*1954T>G (n.*1954T>G) c.546T>G c.295T>G c.2051T>G (p.Ile684Ser) | gnomAD v4 |
16 | g.68695860C>A | CA496157993 | CDH3 | c.2217C>A (p.Ile739=) c.36C>A (p.Ile12=) c.*1955C>A (n.*1955C>A) c.547C>A c.296C>A c.2052C>A (p.Ile684=) | |
16 | g.68695860C= | CA2229920524 | CDH3 | c.2217C= (p.Ile739=) c.36C= (p.Ile12=) c.*1955C= (n.*1955C=) c.547C= c.296C= c.2052C= (p.Ile684=) | |
16 | g.68695860C>G | CA396456321 | CDH3 | c.2217C>G (p.Ile739Met) c.36C>G (p.Ile12Met) c.*1955C>G (n.*1955C>G) c.547C>G c.296C>G c.2052C>G (p.Ile684Met) | |
16 | g.68695860C>T | CA8129621 | CDH3 | c.2217C>T (p.Ile739=) c.36C>T (p.Ile12=) c.*1955C>T (n.*1955C>T) c.547C>T c.296C>T c.2052C>T (p.Ile684=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.68695861C>A | CA396456322 | CDH3 | c.2218C>A (p.Pro740Thr) c.37C>A (p.Pro13Thr) c.*1956C>A (n.*1956C>A) c.548C>A c.297C>A c.2053C>A (p.Pro685Thr) | |
16 | g.68695861C= | CA2229920526 | CDH3 | c.2218C= (p.Pro740=) c.37C= (p.Pro13=) c.*1956C= (n.*1956C=) c.548C= c.297C= c.2053C= (p.Pro685=) | |
16 | g.68695861C>G | CA396456323 | CDH3 | c.2218C>G (p.Pro740Ala) c.37C>G (p.Pro13Ala) c.*1956C>G (n.*1956C>G) c.548C>G c.297C>G c.2053C>G (p.Pro685Ala) | ClinVar dbSNP |
16 | g.68695861C>T | CA396456324 | CDH3 | c.2218C>T (p.Pro740Ser) c.37C>T (p.Pro13Ser) c.*1956C>T (n.*1956C>T) c.548C>T c.297C>T c.2053C>T (p.Pro685Ser) | |
16 | g.68695862C>A | CA396456325 | CDH3 | c.2219C>A (p.Pro740Gln) c.38C>A (p.Pro13Gln) c.*1957C>A (n.*1957C>A) c.549C>A c.298C>A c.2054C>A (p.Pro685Gln) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.68695862C= | CA2229920535 | CDH3 | c.2219C= (p.Pro740=) c.38C= (p.Pro13=) c.*1957C= (n.*1957C=) c.549C= c.298C= c.2054C= (p.Pro685=) | |
16 | g.68695862C>G | CA283289502 | CDH3 | c.2219C>G (p.Pro740Arg) c.38C>G (p.Pro13Arg) c.*1957C>G (n.*1957C>G) c.549C>G c.298C>G c.2054C>G (p.Pro685Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695862C>T | CA8129622 | CDH3 | c.2219C>T (p.Pro740Leu) c.38C>T (p.Pro13Leu) c.*1957C>T (n.*1957C>T) c.549C>T c.298C>T c.2054C>T (p.Pro685Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695863G>A | CA8129623 | CDH3 | c.2220G>A (p.Pro740=) c.39G>A (p.Pro13=) c.*1958G>A (n.*1958G>A) c.550G>A c.299G>A c.2055G>A (p.Pro685=) | ClinVar dbSNP ExAC gnomAD v4 |
16 | g.68695863G>C | CA496158006 | CDH3 | c.2220G>C (p.Pro740=) c.39G>C (p.Pro13=) c.*1958G>C (n.*1958G>C) c.550G>C c.299G>C c.2055G>C (p.Pro685=) | |
16 | g.68695863G= | CA2229920537 | CDH3 | c.2220G= (p.Pro740=) c.39G= (p.Pro13=) c.*1958G= (n.*1958G=) c.550G= c.299G= c.2055G= (p.Pro685=) | |
16 | g.68695863G>T | CA496158005 | CDH3 | c.2220G>T (p.Pro740=) c.39G>T (p.Pro13=) c.*1958G>T (n.*1958G>T) c.550G>T c.299G>T c.2055G>T (p.Pro685=) | |
16 | g.68695864A>C | CA396456326 | CDH3 | c.2221A>C (p.Thr741Pro) c.40A>C (p.Thr14Pro) c.*1959A>C (n.*1959A>C) c.551A>C c.300A>C c.2056A>C (p.Thr686Pro) | |
16 | g.68695864A>G | CA396456327 | CDH3 | c.2221A>G (p.Thr741Ala) c.40A>G (p.Thr14Ala) c.*1959A>G (n.*1959A>G) c.551A>G c.300A>G c.2056A>G (p.Thr686Ala) | |
16 | g.68695864A>T | CA396456328 | CDH3 | c.2221A>T (p.Thr741Ser) c.40A>T (p.Thr14Ser) c.*1959A>T (n.*1959A>T) c.551A>T c.300A>T c.2056A>T (p.Thr686Ser) | |
16 | g.68695865C>A | CA396456331 | CDH3 | c.2222C>A (p.Thr741Lys) c.41C>A (p.Thr14Lys) c.*1960C>A (n.*1960C>A) c.552C>A c.301C>A c.2057C>A (p.Thr686Lys) | |
16 | g.68695865C= | CA2229920540 | CDH3 | c.2222C= (p.Thr741=) c.41C= (p.Thr14=) c.*1960C= (n.*1960C=) c.552C= c.301C= c.2057C= (p.Thr686=) | |
16 | g.68695865C>G | CA396456329 | CDH3 | c.2222C>G (p.Thr741Arg) c.41C>G (p.Thr14Arg) c.*1960C>G (n.*1960C>G) c.552C>G c.301C>G c.2057C>G (p.Thr686Arg) | |
16 | g.68695865C>T | CA396456330 | CDH3 | c.2222C>T (p.Thr741Ile) c.41C>T (p.Thr14Ile) c.*1960C>T (n.*1960C>T) c.552C>T c.301C>T c.2057C>T (p.Thr686Ile) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.68695866A= | CA2229920542 | CDH3 | c.2223A= (p.Thr741=) c.42A= (p.Thr14=) c.*1961A= (n.*1961A=) c.553A= c.302A= c.2058A= (p.Thr686=) | |
16 | g.68695866A>C | CA496158015 | CDH3 | c.2223A>C (p.Thr741=) c.42A>C (p.Thr14=) c.*1961A>C (n.*1961A>C) c.553A>C c.302A>C c.2058A>C (p.Thr686=) | dbSNP |
16 | g.68695866A>G | CA496158018 | CDH3 | c.2223A>G (p.Thr741=) c.42A>G (p.Thr14=) c.*1961A>G (n.*1961A>G) c.553A>G c.302A>G c.2058A>G (p.Thr686=) | |
16 | g.68695866A>T | CA496158016 | CDH3 | c.2223A>T (p.Thr741=) c.42A>T (p.Thr14=) c.*1961A>T (n.*1961A>T) c.553A>T c.302A>T c.2058A>T (p.Thr686=) | |
16 | g.68695867C>A | CA396456332 | CDH3 | c.2224C>A (p.Pro742Thr) c.43C>A (p.Pro15Thr) c.*1962C>A (n.*1962C>A) c.554C>A c.303C>A c.2059C>A (p.Pro687Thr) | |
16 | g.68695867C>G | CA396456333 | CDH3 | c.2224C>G (p.Pro742Ala) c.43C>G (p.Pro15Ala) c.*1962C>G (n.*1962C>G) c.554C>G c.303C>G c.2059C>G (p.Pro687Ala) | |
16 | g.68695867C>T | CA396456334 | CDH3 | c.2224C>T (p.Pro742Ser) c.43C>T (p.Pro15Ser) c.*1962C>T (n.*1962C>T) c.554C>T c.303C>T c.2059C>T (p.Pro687Ser) | |
16 | g.68695868C>A | CA396456335 | CDH3 | c.2225C>A (p.Pro742His) c.44C>A (p.Pro15His) c.*1963C>A (n.*1963C>A) c.555C>A c.304C>A c.2060C>A (p.Pro687His) | |
16 | g.68695868C>G | CA396456336 | CDH3 | c.2225C>G (p.Pro742Arg) c.44C>G (p.Pro15Arg) c.*1963C>G (n.*1963C>G) c.555C>G c.304C>G c.2060C>G (p.Pro687Arg) | |
16 | g.68695868C>T | CA396456337 | CDH3 | c.2225C>T (p.Pro742Leu) c.44C>T (p.Pro15Leu) c.*1963C>T (n.*1963C>T) c.555C>T c.304C>T c.2060C>T (p.Pro687Leu) | gnomAD v4 |
16 | g.68695869C>A | CA496158027 | CDH3 | c.2226C>A (p.Pro742=) c.45C>A (p.Pro15=) c.*1964C>A (n.*1964C>A) c.556C>A c.305C>A c.2061C>A (p.Pro687=) | |
16 | g.68695869C= | CA2229920544 | CDH3 | c.2226C= (p.Pro742=) c.45C= (p.Pro15=) c.*1964C= (n.*1964C=) c.556C= c.305C= c.2061C= (p.Pro687=) | |
16 | g.68695869C>G | CA496158028 | CDH3 | c.2226C>G (p.Pro742=) c.45C>G (p.Pro15=) c.*1964C>G (n.*1964C>G) c.556C>G c.305C>G c.2061C>G (p.Pro687=) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.68695869C>T | CA496158031 | CDH3 | c.2226C>T (p.Pro742=) c.45C>T (p.Pro15=) c.*1964C>T (n.*1964C>T) c.556C>T c.305C>T c.2061C>T (p.Pro687=) | |
16 | g.68695870A= | CA2229920549 | CDH3 | c.2227A= (p.Met743=) c.46A= (p.Met16=) c.*1965A= (n.*1965A=) c.557A= c.306A= c.2062A= (p.Met688=) | |
16 | g.68695870A>C | CA396456338 | CDH3 | c.2227A>C (p.Met743Leu) c.46A>C (p.Met16Leu) c.*1965A>C (n.*1965A>C) c.557A>C c.306A>C c.2062A>C (p.Met688Leu) | |
16 | g.68695870A>G | CA8129624 | CDH3 | c.2227A>G (p.Met743Val) c.46A>G (p.Met16Val) c.*1965A>G (n.*1965A>G) c.557A>G c.306A>G c.2062A>G (p.Met688Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695870A>T | CA396456339 | CDH3 | c.2227A>T (p.Met743Leu) c.46A>T (p.Met16Leu) c.*1965A>T (n.*1965A>T) c.557A>T c.306A>T c.2062A>T (p.Met688Leu) | |
16 | g.68695871T>A | CA396456340 | CDH3 | c.2228T>A (p.Met743Lys) c.47T>A (p.Met16Lys) c.*1966T>A (n.*1966T>A) c.558T>A c.307T>A c.2063T>A (p.Met688Lys) | |
16 | g.68695871T>C | CA8129625 | CDH3 | c.2228T>C (p.Met743Thr) c.47T>C (p.Met16Thr) c.*1966T>C (n.*1966T>C) c.558T>C c.307T>C c.2063T>C (p.Met688Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.68695871T>G | CA396456341 | CDH3 | c.2228T>G (p.Met743Arg) c.47T>G (p.Met16Arg) c.*1966T>G (n.*1966T>G) c.558T>G c.307T>G c.2063T>G (p.Met688Arg) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.68695871T= | CA2229920556 | CDH3 | c.2228T= (p.Met743=) c.47T= (p.Met16=) c.*1966T= (n.*1966T=) c.558T= c.307T= c.2063T= (p.Met688=) | |
16 | g.68695872G>A | CA8129626 | CDH3 | c.2229G>A (p.Met743Ile) c.48G>A (p.Met16Ile) c.*1967G>A (n.*1967G>A) c.559G>A c.308G>A c.2064G>A (p.Met688Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.68695872G>C | CA396456343 | CDH3 | c.2229G>C (p.Met743Ile) c.48G>C (p.Met16Ile) c.*1967G>C (n.*1967G>C) c.559G>C c.308G>C c.2064G>C (p.Met688Ile) | |
16 | g.68695872G= | CA2229920559 | CDH3 | c.2229G= (p.Met743=) c.48G= (p.Met16=) c.*1967G= (n.*1967G=) c.559G= c.308G= c.2064G= (p.Met688=) | |
16 | g.68695872G>T | CA396456342 | CDH3 | c.2229G>T (p.Met743Ile) c.48G>T (p.Met16Ile) c.*1967G>T (n.*1967G>T) c.559G>T c.308G>T c.2064G>T (p.Met688Ile) | |
16 | g.68695873T>A | CA396456346 | CDH3 | c.2230T>A (p.Tyr744Asn) c.49T>A (p.Tyr17Asn) c.*1968T>A (n.*1968T>A) c.560T>A c.309T>A c.2065T>A (p.Tyr689Asn) | |
16 | g.68695873T>C | CA396456344 | CDH3 | c.2230T>C (p.Tyr744His) c.49T>C (p.Tyr17His) c.*1968T>C (n.*1968T>C) c.560T>C c.309T>C c.2065T>C (p.Tyr689His) | ClinVar dbSNP |
16 | g.68695873T>G | CA396456345 | CDH3 | c.2230T>G (p.Tyr744Asp) c.49T>G (p.Tyr17Asp) c.*1968T>G (n.*1968T>G) c.560T>G c.309T>G c.2065T>G (p.Tyr689Asp) | |
16 | g.68695873T= | CA2229920561 | CDH3 | c.2230T= (p.Tyr744=) c.49T= (p.Tyr17=) c.*1968T= (n.*1968T=) c.560T= c.309T= c.2065T= (p.Tyr689=) | |
16 | g.68695874A= | CA2229920564 | CDH3 | c.2231A= (p.Tyr744=) c.50A= (p.Tyr17=) c.*1969A= (n.*1969A=) c.561A= c.310A= c.2066A= (p.Tyr689=) | |
16 | g.68695874A>C | CA396456347 | CDH3 | c.2231A>C (p.Tyr744Ser) c.50A>C (p.Tyr17Ser) c.*1969A>C (n.*1969A>C) c.561A>C c.310A>C c.2066A>C (p.Tyr689Ser) | dbSNP |
16 | g.68695874A>G | CA396456348 | CDH3 | c.2231A>G (p.Tyr744Cys) c.50A>G (p.Tyr17Cys) c.*1969A>G (n.*1969A>G) c.561A>G c.310A>G c.2066A>G (p.Tyr689Cys) | |
16 | g.68695874A>T | CA396456349 | CDH3 | c.2231A>T (p.Tyr744Phe) c.50A>T (p.Tyr17Phe) c.*1969A>T (n.*1969A>T) c.561A>T c.310A>T c.2066A>T (p.Tyr689Phe) | |
16 | g.68695875C>A | CA396456351 | CDH3 | c.2232C>A (p.Tyr744Ter) c.51C>A (p.Tyr17Ter) c.*1970C>A (n.*1970C>A) c.562C>A c.311C>A c.2067C>A (p.Tyr689Ter) | |
16 | g.68695875C= | CA2229920566 | CDH3 | c.2232C= (p.Tyr744=) c.51C= (p.Tyr17=) c.*1970C= (n.*1970C=) c.562C= c.311C= c.2067C= (p.Tyr689=) | |
16 | g.68695875C>G | CA396456350 | CDH3 | c.2232C>G (p.Tyr744Ter) c.51C>G (p.Tyr17Ter) c.*1970C>G (n.*1970C>G) c.562C>G c.311C>G c.2067C>G (p.Tyr689Ter) | |
16 | g.68695875C>T | CA8129627 | CDH3 | c.2232C>T (p.Tyr744=) c.51C>T (p.Tyr17=) c.*1970C>T (n.*1970C>T) c.562C>T c.311C>T c.2067C>T (p.Tyr689=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695876C>A | CA396456352 | CDH3 | c.2233C>A (p.Arg745Ser) c.52C>A (p.Arg18Ser) c.*1971C>A (n.*1971C>A) c.563C>A c.312C>A c.2068C>A (p.Arg690Ser) | |
16 | g.68695876C= | CA2229920575 | CDH3 | c.2233C= (p.Arg745=) c.52C= (p.Arg18=) c.*1971C= (n.*1971C=) c.563C= c.312C= c.2068C= (p.Arg690=) | |
16 | g.68695876C>G | CA396456353 | CDH3 | c.2233C>G (p.Arg745Gly) c.52C>G (p.Arg18Gly) c.*1971C>G (n.*1971C>G) c.563C>G c.312C>G c.2068C>G (p.Arg690Gly) | |
16 | g.68695876C>T | CA16620221 | CDH3 | c.2233C>T (p.Arg745Cys) c.52C>T (p.Arg18Cys) c.*1971C>T (n.*1971C>T) c.563C>T c.312C>T c.2068C>T (p.Arg690Cys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695877G>A | CA396456354 | CDH3 | c.2234G>A (p.Arg745His) c.53G>A (p.Arg18His) c.*1972G>A (n.*1972G>A) c.564G>A c.313G>A c.2069G>A (p.Arg690His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695877G>C | CA396456355 | CDH3 | c.2234G>C (p.Arg745Pro) c.53G>C (p.Arg18Pro) c.*1972G>C (n.*1972G>C) c.564G>C c.313G>C c.2069G>C (p.Arg690Pro) | |
16 | g.68695877G= | CA2229920580 | CDH3 | c.2234G= (p.Arg745=) c.53G= (p.Arg18=) c.*1972G= (n.*1972G=) c.564G= c.313G= c.2069G= (p.Arg690=) | |
16 | g.68695877G>T | CA396456356 | CDH3 | c.2234G>T (p.Arg745Leu) c.53G>T (p.Arg18Leu) c.*1972G>T (n.*1972G>T) c.564G>T c.313G>T c.2069G>T (p.Arg690Leu) | |
16 | g.68695878T>A | CA496158053 | CDH3 | c.2235T>A (p.Arg745=) c.54T>A (p.Arg18=) c.*1973T>A (n.*1973T>A) c.565T>A c.314T>A c.2070T>A (p.Arg690=) | |
16 | g.68695878T>C | CA496158054 | CDH3 | c.2235T>C (p.Arg745=) c.54T>C (p.Arg18=) c.*1973T>C (n.*1973T>C) c.565T>C c.314T>C c.2070T>C (p.Arg690=) | gnomAD v4 |
16 | g.68695878T>G | CA496158056 | CDH3 | c.2235T>G (p.Arg745=) c.54T>G (p.Arg18=) c.*1973T>G (n.*1973T>G) c.565T>G c.314T>G c.2070T>G (p.Arg690=) | |
16 | g.68695879C>A | CA396456357 | CDH3 | c.2236C>A (p.Pro746Thr) c.55C>A (p.Pro19Thr) c.*1974C>A (n.*1974C>A) c.566C>A c.315C>A c.2071C>A (p.Pro691Thr) | dbSNP gnomAD v4 |
16 | g.68695879C= | CA2229920583 | CDH3 | c.2236C= (p.Pro746=) c.55C= (p.Pro19=) c.*1974C= (n.*1974C=) c.566C= c.315C= c.2071C= (p.Pro691=) | |
16 | g.68695879C>G | CA396456359 | CDH3 | c.2236C>G (p.Pro746Ala) c.55C>G (p.Pro19Ala) c.*1974C>G (n.*1974C>G) c.566C>G c.315C>G c.2071C>G (p.Pro691Ala) | |
16 | g.68695879C>T | CA396456358 | CDH3 | c.2236C>T (p.Pro746Ser) c.55C>T (p.Pro19Ser) c.*1974C>T (n.*1974C>T) c.566C>T c.315C>T c.2071C>T (p.Pro691Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
16 | g.68695880C>A | CA396456360 | CDH3 | c.2237C>A (p.Pro746His) c.56C>A (p.Pro19His) c.*1975C>A (n.*1975C>A) c.567C>A c.316C>A c.2072C>A (p.Pro691His) | |
16 | g.68695880C>G | CA396456361 | CDH3 | c.2237C>G (p.Pro746Arg) c.56C>G (p.Pro19Arg) c.*1975C>G (n.*1975C>G) c.567C>G c.316C>G c.2072C>G (p.Pro691Arg) | |
16 | g.68695880C>T | CA396456362 | CDH3 | c.2237C>T (p.Pro746Leu) c.56C>T (p.Pro19Leu) c.*1975C>T (n.*1975C>T) c.567C>T c.316C>T c.2072C>T (p.Pro691Leu) | gnomAD v4 |
16 | g.68695881T>A | CA496158065 | CDH3 | c.2238T>A (p.Pro746=) c.57T>A (p.Pro19=) c.*1976T>A (n.*1976T>A) c.568T>A c.317T>A c.2073T>A (p.Pro691=) | |
16 | g.68695881T>C | CA496158069 | CDH3 | c.2238T>C (p.Pro746=) c.57T>C (p.Pro19=) c.*1976T>C (n.*1976T>C) c.568T>C c.317T>C c.2073T>C (p.Pro691=) | |
16 | g.68695881T>G | CA496158067 | CDH3 | c.2238T>G (p.Pro746=) c.57T>G (p.Pro19=) c.*1976T>G (n.*1976T>G) c.568T>G c.317T>G c.2073T>G (p.Pro691=) | |
16 | g.68695881_68695882delinsCA | CA2580091832 | CDH3 | c.2238_2239delinsCA (p.Pro746=) c.57_58delinsCA (p.Pro19=) c.*1976_*1977delinsCA (n.*1976_*1977delinsCA) c.568_569delinsCA c.317_318delinsCA c.2073_2074delinsCA (p.Pro691=) | ClinVar |
16 | g.68695882C>A | CA147289 | CDH3 | c.2239C>A (p.Arg747=) c.58C>A (p.Arg20=) c.*1977C>A (n.*1977C>A) c.569C>A c.318C>A c.2074C>A (p.Arg692=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695882C= | CA2229920591 | CDH3 | c.2239C= (p.Arg747=) c.58C= (p.Arg20=) c.*1977C= (n.*1977C=) c.569C= c.318C= c.2074C= (p.Arg692=) | |
16 | g.68695882C>G | CA396456363 | CDH3 | c.2239C>G (p.Arg747Gly) c.58C>G (p.Arg20Gly) c.*1977C>G (n.*1977C>G) c.569C>G c.318C>G c.2074C>G (p.Arg692Gly) | |
16 | g.68695882C>T | CA396456364 | CDH3 | c.2239C>T (p.Arg747Trp) c.58C>T (p.Arg20Trp) c.*1977C>T (n.*1977C>T) c.569C>T c.318C>T c.2074C>T (p.Arg692Trp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68695882_68695883delinsAA | CA1139664735 | CDH3 | c.2239_2240delinsAA (p.Arg747Lys) c.58_59delinsAA (p.Arg20Lys) c.*1977_*1978delinsAA (n.*1977_*1978delinsAA) c.569_570delinsAA c.318_319delinsAA c.2074_2075delinsAA (p.Arg692Lys) | ClinVar dbSNP |
16 | g.68695882_68695883delinsCG | CA2229920596 | CDH3 | c.2239_2240delinsCG (p.Arg747=) c.58_59delinsCG (p.Arg20=) c.*1977_*1978delinsCG (n.*1977_*1978delinsCG) c.569_570delinsCG c.318_319delinsCG c.2074_2075delinsCG (p.Arg692=) |