Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.7582933_7587670delinsAGAACAGTCTT | CA2580075482 | ClinVar | ||
6 | g.7582933_7587670delinsAGAGAAGAACAGTCTT | CA915944145 | ClinVar | ||
6 | g.7582934_7587655del | CA2695202641 | |||
6 | g.7583301_7585800del | CA006686 | DSP | c.4710_7209del (p.Gly1571GlufsTer?) c.6039_8538del (p.Gly2014GlufsTer?) c.4242_6741del (p.Gly1415GlufsTer?) | |
6 | g.7584391_7584414del | CA2573140820 | DSP | c.5800_5823del (p.Ile1934_His1941del) c.7129_7152del (p.Ile2377_His2384del) c.5332_5355del (p.Ile1778_His1785del) | ClinVar dbSNP |
6 | g.7584407_7584423del | CA2677219518 | DSP | c.5816_5832del (p.Glu1939GlyfsTer2) c.7145_7161del (p.Glu2382GlyfsTer2) c.5348_5364del (p.Glu1783GlyfsTer2) | gnomAD v4 |
6 | g.7584412C>A | CA362692346 | DSP | c.5821C>A (p.His1941Asn) c.7150C>A (p.His2384Asn) c.5353C>A (p.His1785Asn) | gnomAD v4 |
6 | g.7584412C>G | CA362692347 | DSP | c.5821C>G (p.His1941Asp) c.7150C>G (p.His2384Asp) c.5353C>G (p.His1785Asp) | |
6 | g.7584412C>T | CA362692348 | DSP | c.5821C>T (p.His1941Tyr) c.7150C>T (p.His2384Tyr) c.5353C>T (p.His1785Tyr) | |
6 | g.7584413A>C | CA362692351 | DSP | c.5822A>C (p.His1941Pro) c.7151A>C (p.His2384Pro) c.5354A>C (p.His1785Pro) | |
6 | g.7584413A>G | CA362692350 | DSP | c.5822A>G (p.His1941Arg) c.7151A>G (p.His2384Arg) c.5354A>G (p.His1785Arg) | |
6 | g.7584413A>T | CA362692349 | DSP | c.5822A>T (p.His1941Leu) c.7151A>T (p.His2384Leu) c.5354A>T (p.His1785Leu) | |
6 | g.7584414T>A | CA362692352 | DSP | c.5823T>A (p.His1941Gln) c.7152T>A (p.His2384Gln) c.5355T>A (p.His1785Gln) | |
6 | g.7584414T>C | CA448716520 | DSP | c.5823T>C (p.His1941=) c.7152T>C (p.His2384=) c.5355T>C (p.His1785=) | |
6 | g.7584414T>G | CA362692353 | DSP | c.5823T>G (p.His1941Gln) c.7152T>G (p.His2384Gln) c.5355T>G (p.His1785Gln) | |
6 | g.7584415C>A | CA362692354 | DSP | c.5824C>A (p.Arg1942Ser) c.7153C>A (p.Arg2385Ser) c.5356C>A (p.Arg1786Ser) | gnomAD v4 |
6 | g.7584415C= | CA1608611114 | DSP | c.5824C= (p.Arg1942=) c.7153C= (p.Arg2385=) c.5356C= (p.Arg1786=) | |
6 | g.7584415C>G | CA362692355 | DSP | c.5824C>G (p.Arg1942Gly) c.7153C>G (p.Arg2385Gly) c.5356C>G (p.Arg1786Gly) | |
6 | g.7584415C>T | CA049214 | DSP | c.5824C>T (p.Arg1942Cys) c.7153C>T (p.Arg2385Cys) c.5356C>T (p.Arg1786Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.7584416G>A | CA362692356 | DSP | c.5825G>A (p.Arg1942His) c.7154G>A (p.Arg2385His) c.5357G>A (p.Arg1786His) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
6 | g.7584416G>C | CA362692357 | DSP | c.5825G>C (p.Arg1942Pro) c.7154G>C (p.Arg2385Pro) c.5357G>C (p.Arg1786Pro) | |
6 | g.7584416G= | CA1608611122 | DSP | c.5825G= (p.Arg1942=) c.7154G= (p.Arg2385=) c.5357G= (p.Arg1786=) | |
6 | g.7584416G>T | CA362692358 | DSP | c.5825G>T (p.Arg1942Leu) c.7154G>T (p.Arg2385Leu) c.5357G>T (p.Arg1786Leu) | |
6 | g.7584417T>A | CA448716532 | DSP | c.5826T>A (p.Arg1942=) c.7155T>A (p.Arg2385=) c.5358T>A (p.Arg1786=) | |
6 | g.7584417T>C | CA448716534 | DSP | c.5826T>C (p.Arg1942=) c.7155T>C (p.Arg2385=) c.5358T>C (p.Arg1786=) | |
6 | g.7584417T>G | CA448716533 | DSP | c.5826T>G (p.Arg1942=) c.7155T>G (p.Arg2385=) c.5358T>G (p.Arg1786=) | |
6 | g.7584418T>A | CA362692359 | DSP | c.5827T>A (p.Leu1943Ile) c.7156T>A (p.Leu2386Ile) c.5359T>A (p.Leu1787Ile) | |
6 | g.7584418T>C | CA448716536 | DSP | c.5827T>C (p.Leu1943=) c.7156T>C (p.Leu2386=) c.5359T>C (p.Leu1787=) | gnomAD v4 |
6 | g.7584418T>G | CA362692360 | DSP | c.5827T>G (p.Leu1943Val) c.7156T>G (p.Leu2386Val) c.5359T>G (p.Leu1787Val) | |
6 | g.7584419T>A | CA362692361 | DSP | c.5828T>A (p.Leu1943Ter) c.7157T>A (p.Leu2386Ter) c.5360T>A (p.Leu1787Ter) | |
6 | g.7584419T>C | CA362692362 | DSP | c.5828T>C (p.Leu1943Ser) c.7157T>C (p.Leu2386Ser) c.5360T>C (p.Leu1787Ser) | gnomAD v4 |
6 | g.7584419T>G | CA362692363 | DSP | c.5828T>G (p.Leu1943Ter) c.7157T>G (p.Leu2386Ter) c.5360T>G (p.Leu1787Ter) | |
6 | g.7584420A>C | CA362692364 | DSP | c.5829A>C (p.Leu1943Phe) c.7158A>C (p.Leu2386Phe) c.5361A>C (p.Leu1787Phe) | |
6 | g.7584420A>G | CA448716543 | DSP | c.5829A>G (p.Leu1943=) c.7158A>G (p.Leu2386=) c.5361A>G (p.Leu1787=) | |
6 | g.7584420A>T | CA362692365 | DSP | c.5829A>T (p.Leu1943Phe) c.7158A>T (p.Leu2386Phe) c.5361A>T (p.Leu1787Phe) | |
6 | g.7584421C>A | CA362692366 | DSP | c.5830C>A (p.Pro1944Thr) c.7159C>A (p.Pro2387Thr) c.5362C>A (p.Pro1788Thr) | |
6 | g.7584421C>G | CA362692369 | DSP | c.5830C>G (p.Pro1944Ala) c.7159C>G (p.Pro2387Ala) c.5362C>G (p.Pro1788Ala) | |
6 | g.7584421C>T | CA362692367 | DSP | c.5830C>T (p.Pro1944Ser) c.7159C>T (p.Pro2387Ser) c.5362C>T (p.Pro1788Ser) | |
6 | g.7584422C>A | CA362692370 | DSP | c.5831C>A (p.Pro1944Gln) c.7160C>A (p.Pro2387Gln) c.5363C>A (p.Pro1788Gln) | |
6 | g.7584422C= | CA1608611132 | DSP | c.5831C= (p.Pro1944=) c.7160C= (p.Pro2387=) c.5363C= (p.Pro1788=) | |
6 | g.7584422C>G | CA362692371 | DSP | c.5831C>G (p.Pro1944Arg) c.7160C>G (p.Pro2387Arg) c.5363C>G (p.Pro1788Arg) | |
6 | g.7584422C>T | CA049230 | DSP | c.5831C>T (p.Pro1944Leu) c.7160C>T (p.Pro2387Leu) c.5363C>T (p.Pro1788Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.7584423A>C | CA448716561 | DSP | c.5832A>C (p.Pro1944=) c.7161A>C (p.Pro2387=) c.5364A>C (p.Pro1788=) | |
6 | g.7584423A>G | CA448716562 | DSP | c.5832A>G (p.Pro1944=) c.7161A>G (p.Pro2387=) c.5364A>G (p.Pro1788=) | |
6 | g.7584423A>T | CA448716564 | DSP | c.5832A>T (p.Pro1944=) c.7161A>T (p.Pro2387=) c.5364A>T (p.Pro1788=) | |
6 | g.7584424G>A | CA049243 | DSP | c.5833G>A (p.Val1945Ile) c.7162G>A (p.Val2388Ile) c.5365G>A (p.Val1789Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.7584424G>C | CA362692372 | DSP | c.5833G>C (p.Val1945Leu) c.7162G>C (p.Val2388Leu) c.5365G>C (p.Val1789Leu) | |
6 | g.7584424G= | CA1608611139 | DSP | c.5833G= (p.Val1945=) c.7162G= (p.Val2388=) c.5365G= (p.Val1789=) | |
6 | g.7584424G>T | CA362692373 | DSP | c.5833G>T (p.Val1945Phe) c.7162G>T (p.Val2388Phe) c.5365G>T (p.Val1789Phe) | |
6 | g.7584425T>A | CA362692374 | DSP | c.5834T>A (p.Val1945Asp) c.7163T>A (p.Val2388Asp) c.5366T>A (p.Val1789Asp) |