Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.122284326C>A | CA354159655 | CASR | c.2141C>A (p.Ala714Asp) c.2402C>A (p.Ala801Asp) c.2372C>A (p.Ala791Asp) c.1889C>A (p.Ala630Asp) c.1784C>A (p.Ala595Asp) | COSMIC |
3 | g.122284326C>G | CA354159654 | CASR | c.2141C>G (p.Ala714Gly) c.2402C>G (p.Ala801Gly) c.2372C>G (p.Ala791Gly) c.1889C>G (p.Ala630Gly) c.1784C>G (p.Ala595Gly) | |
3 | g.122284326C>T | CA354159653 | CASR | c.2141C>T (p.Ala714Val) c.2402C>T (p.Ala801Val) c.2372C>T (p.Ala791Val) c.1889C>T (p.Ala630Val) c.1784C>T (p.Ala595Val) | gnomAD v4 |
3 | g.122284327C>A | CA435425145 | CASR | c.2142C>A (p.Ala714=) c.2403C>A (p.Ala801=) c.2373C>A (p.Ala791=) c.1890C>A (p.Ala630=) c.1785C>A (p.Ala595=) | |
3 | g.122284327C= | CA1397872190 | CASR | c.2142C= (p.Ala714=) c.2403C= (p.Ala801=) c.2373C= (p.Ala791=) c.1890C= (p.Ala630=) c.1785C= (p.Ala595=) | |
3 | g.122284327C>G | CA435425146 | CASR | c.2142C>G (p.Ala714=) c.2403C>G (p.Ala801=) c.2373C>G (p.Ala791=) c.1890C>G (p.Ala630=) c.1785C>G (p.Ala595=) | |
3 | g.122284327C>T | CA435425148 | CASR | c.2142C>T (p.Ala714=) c.2403C>T (p.Ala801=) c.2373C>T (p.Ala791=) c.1890C>T (p.Ala630=) c.1785C>T (p.Ala595=) | ClinVar dbSNP |
3 | g.122284328T>A | CA354159656 | CASR | c.2143T>A (p.Phe715Ile) c.2404T>A (p.Phe802Ile) c.2374T>A (p.Phe792Ile) c.1891T>A (p.Phe631Ile) c.1786T>A (p.Phe596Ile) | |
3 | g.122284328T>C | CA354159657 | CASR | c.2143T>C (p.Phe715Leu) c.2404T>C (p.Phe802Leu) c.2374T>C (p.Phe792Leu) c.1891T>C (p.Phe631Leu) c.1786T>C (p.Phe596Leu) | |
3 | g.122284328T>G | CA354159658 | CASR | c.2143T>G (p.Phe715Val) c.2404T>G (p.Phe802Val) c.2374T>G (p.Phe792Val) c.1891T>G (p.Phe631Val) c.1786T>G (p.Phe596Val) | |
3 | g.122284329T>A | CA354159659 | CASR | c.2144T>A (p.Phe715Tyr) c.2405T>A (p.Phe802Tyr) c.2375T>A (p.Phe792Tyr) c.1892T>A (p.Phe631Tyr) c.1787T>A (p.Phe596Tyr) | |
3 | g.122284329T>C | CA354159660 | CASR | c.2144T>C (p.Phe715Ser) c.2405T>C (p.Phe802Ser) c.2375T>C (p.Phe792Ser) c.1892T>C (p.Phe631Ser) c.1787T>C (p.Phe596Ser) | |
3 | g.122284329T>G | CA354159661 | CASR | c.2144T>G (p.Phe715Cys) c.2405T>G (p.Phe802Cys) c.2375T>G (p.Phe792Cys) c.1892T>G (p.Phe631Cys) c.1787T>G (p.Phe596Cys) | |
3 | g.122284330C>A | CA354159662 | CASR | c.2145C>A (p.Phe715Leu) c.2406C>A (p.Phe802Leu) c.2376C>A (p.Phe792Leu) c.1893C>A (p.Phe631Leu) c.1788C>A (p.Phe596Leu) | |
3 | g.122284330C= | CA1397872196 | CASR | c.2145C= (p.Phe715=) c.2406C= (p.Phe802=) c.2376C= (p.Phe792=) c.1893C= (p.Phe631=) c.1788C= (p.Phe596=) | |
3 | g.122284330C>G | CA354159663 | CASR | c.2145C>G (p.Phe715Leu) c.2406C>G (p.Phe802Leu) c.2376C>G (p.Phe792Leu) c.1893C>G (p.Phe631Leu) c.1788C>G (p.Phe596Leu) | |
3 | g.122284330C>T | CA435425150 | CASR | c.2145C>T (p.Phe715=) c.2406C>T (p.Phe802=) c.2376C>T (p.Phe792=) c.1893C>T (p.Phe631=) c.1788C>T (p.Phe596=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.122284331A>C | CA354159664 | CASR | c.2146A>C (p.Lys716Gln) c.2407A>C (p.Lys803Gln) c.2377A>C (p.Lys793Gln) c.1894A>C (p.Lys632Gln) c.1789A>C (p.Lys597Gln) | |
3 | g.122284331A>G | CA354159665 | CASR | c.2146A>G (p.Lys716Glu) c.2407A>G (p.Lys803Glu) c.2377A>G (p.Lys793Glu) c.1894A>G (p.Lys632Glu) c.1789A>G (p.Lys597Glu) | |
3 | g.122284331A>T | CA354159666 | CASR | c.2146A>T (p.Lys716Ter) c.2407A>T (p.Lys803Ter) c.2377A>T (p.Lys793Ter) c.1894A>T (p.Lys632Ter) c.1789A>T (p.Lys597Ter) | |
3 | g.122284332A>C | CA354159669 | CASR | c.2147A>C (p.Lys716Thr) c.2408A>C (p.Lys803Thr) c.2378A>C (p.Lys793Thr) c.1895A>C (p.Lys632Thr) c.1790A>C (p.Lys597Thr) | |
3 | g.122284332A>G | CA354159668 | CASR | c.2147A>G (p.Lys716Arg) c.2408A>G (p.Lys803Arg) c.2378A>G (p.Lys793Arg) c.1895A>G (p.Lys632Arg) c.1790A>G (p.Lys597Arg) | |
3 | g.122284332A>T | CA354159667 | CASR | c.2147A>T (p.Lys716Met) c.2408A>T (p.Lys803Met) c.2378A>T (p.Lys793Met) c.1895A>T (p.Lys632Met) c.1790A>T (p.Lys597Met) | ClinVar |
3 | g.122284333G>A | CA435425151 | CASR | c.2148G>A (p.Lys716=) c.2409G>A (p.Lys803=) c.2379G>A (p.Lys793=) c.1896G>A (p.Lys632=) c.1791G>A (p.Lys597=) | ClinVar dbSNP |
3 | g.122284333G>C | CA354159670 | CASR | c.2148G>C (p.Lys716Asn) c.2409G>C (p.Lys803Asn) c.2379G>C (p.Lys793Asn) c.1896G>C (p.Lys632Asn) c.1791G>C (p.Lys597Asn) | |
3 | g.122284333G>T | CA354159671 | CASR | c.2148G>T (p.Lys716Asn) c.2409G>T (p.Lys803Asn) c.2379G>T (p.Lys793Asn) c.1896G>T (p.Lys632Asn) c.1791G>T (p.Lys597Asn) | |
3 | g.122284334T>A | CA354159672 | CASR | c.2149T>A (p.Ser717Thr) c.2410T>A (p.Ser804Thr) c.2380T>A (p.Ser794Thr) c.1897T>A (p.Ser633Thr) c.1792T>A (p.Ser598Thr) | |
3 | g.122284334T>C | CA354159673 | CASR | c.2149T>C (p.Ser717Pro) c.2410T>C (p.Ser804Pro) c.2380T>C (p.Ser794Pro) c.1897T>C (p.Ser633Pro) c.1792T>C (p.Ser598Pro) | |
3 | g.122284334T>G | CA354159674 | CASR | c.2149T>G (p.Ser717Ala) c.2410T>G (p.Ser804Ala) c.2380T>G (p.Ser794Ala) c.1897T>G (p.Ser633Ala) c.1792T>G (p.Ser598Ala) | ClinVar |
3 | g.122284335C>A | CA354159675 | CASR | c.2150C>A (p.Ser717Tyr) c.2411C>A (p.Ser804Tyr) c.2381C>A (p.Ser794Tyr) c.1898C>A (p.Ser633Tyr) c.1793C>A (p.Ser598Tyr) | |
3 | g.122284335C>G | CA354159676 | CASR | c.2150C>G (p.Ser717Cys) c.2411C>G (p.Ser804Cys) c.2381C>G (p.Ser794Cys) c.1898C>G (p.Ser633Cys) c.1793C>G (p.Ser598Cys) | |
3 | g.122284335C>T | CA354159677 | CASR | c.2150C>T (p.Ser717Phe) c.2411C>T (p.Ser804Phe) c.2381C>T (p.Ser794Phe) c.1898C>T (p.Ser633Phe) c.1793C>T (p.Ser598Phe) | gnomAD v4 |
3 | g.122284337del | CA2580068645 | CASR | c.2152del (p.Arg718GlyfsTer?) c.2413del (p.Arg805GlyfsTer?) c.2383del (p.Arg795GlyfsTer?) c.1900del (p.Arg634GlyfsTer?) c.1795del (p.Arg599GlyfsTer?) | ClinVar dbSNP |
3 | g.122284336C>A | CA435425153 | CASR | c.2151C>A (p.Ser717=) c.2412C>A (p.Ser804=) c.2382C>A (p.Ser794=) c.1899C>A (p.Ser633=) c.1794C>A (p.Ser598=) | |
3 | g.122284336C>G | CA435425154 | CASR | c.2151C>G (p.Ser717=) c.2412C>G (p.Ser804=) c.2382C>G (p.Ser794=) c.1899C>G (p.Ser633=) c.1794C>G (p.Ser598=) | |
3 | g.122284336C>T | CA435425156 | CASR | c.2151C>T (p.Ser717=) c.2412C>T (p.Ser804=) c.2382C>T (p.Ser794=) c.1899C>T (p.Ser633=) c.1794C>T (p.Ser598=) | ClinVar |
3 | g.122284337C>A | CA435425159 | CASR | c.2152C>A (p.Arg718=) c.2413C>A (p.Arg805=) c.2383C>A (p.Arg795=) c.1900C>A (p.Arg634=) c.1795C>A (p.Arg599=) | gnomAD v4 |
3 | g.122284337C= | CA1397872200 | CASR | c.2152C= (p.Arg718=) c.2413C= (p.Arg805=) c.2383C= (p.Arg795=) c.1900C= (p.Arg634=) c.1795C= (p.Arg599=) | |
3 | g.122284337C>G | CA354159678 | CASR | c.2152C>G (p.Arg718Gly) c.2413C>G (p.Arg805Gly) c.2383C>G (p.Arg795Gly) c.1900C>G (p.Arg634Gly) c.1795C>G (p.Arg599Gly) | ClinVar dbSNP |
3 | g.122284337C>T | CA119467 | CASR | c.2152C>T (p.Arg718Trp) c.2413C>T (p.Arg805Trp) c.2383C>T (p.Arg795Trp) c.1900C>T (p.Arg634Trp) c.1795C>T (p.Arg599Trp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.122284338G>A | CA82748943 | CASR | c.2153G>A (p.Arg718Gln) c.2414G>A (p.Arg805Gln) c.2384G>A (p.Arg795Gln) c.1901G>A (p.Arg634Gln) c.1796G>A (p.Arg599Gln) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
3 | g.122284338G>C | CA354159679 | CASR | c.2153G>C (p.Arg718Pro) c.2414G>C (p.Arg805Pro) c.2384G>C (p.Arg795Pro) c.1901G>C (p.Arg634Pro) c.1796G>C (p.Arg599Pro) | ClinVar |
3 | g.122284338G= | CA1397872205 | CASR | c.2153G= (p.Arg718=) c.2414G= (p.Arg805=) c.2384G= (p.Arg795=) c.1901G= (p.Arg634=) c.1796G= (p.Arg599=) | |
3 | g.122284338G>T | CA354159680 | CASR | c.2153G>T (p.Arg718Leu) c.2414G>T (p.Arg805Leu) c.2384G>T (p.Arg795Leu) c.1901G>T (p.Arg634Leu) c.1796G>T (p.Arg599Leu) | ClinVar dbSNP |
3 | g.122284339G>A | CA435425160 | CASR | c.2154G>A (p.Arg718=) c.2415G>A (p.Arg805=) c.2385G>A (p.Arg795=) c.1902G>A (p.Arg634=) c.1797G>A (p.Arg599=) | dbSNP |
3 | g.122284339G>C | CA435425161 | CASR | c.2154G>C (p.Arg718=) c.2415G>C (p.Arg805=) c.2385G>C (p.Arg795=) c.1902G>C (p.Arg634=) c.1797G>C (p.Arg599=) | |
3 | g.122284339G= | CA1397872209 | CASR | c.2154G= (p.Arg718=) c.2415G= (p.Arg805=) c.2385G= (p.Arg795=) c.1902G= (p.Arg634=) c.1797G= (p.Arg599=) | |
3 | g.122284339G>T | CA435425163 | CASR | c.2154G>T (p.Arg718=) c.2415G>T (p.Arg805=) c.2385G>T (p.Arg795=) c.1902G>T (p.Arg634=) c.1797G>T (p.Arg599=) | |
3 | g.122284340A>C | CA354159682 | CASR | c.2155A>C (p.Lys719Gln) c.2416A>C (p.Lys806Gln) c.2386A>C (p.Lys796Gln) c.1903A>C (p.Lys635Gln) c.1798A>C (p.Lys600Gln) | |
3 | g.122284340A>G | CA354159683 | CASR | c.2155A>G (p.Lys719Glu) c.2416A>G (p.Lys806Glu) c.2386A>G (p.Lys796Glu) c.1903A>G (p.Lys635Glu) c.1798A>G (p.Lys600Glu) | dbSNP gnomAD v3 gnomAD v4 |