Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.32435209_32435210delinsGC | CA1962327394 | WT1 | c.151_152delinsGC (p.Ala51=) c.136_137delinsGC (p.Ala46=) n.330_331delinsGC | |
11 | g.32435209_32435210delinsTT | CA2573146211 | WT1 | c.151_152delinsAA (p.Ala51Asn) c.136_137delinsAA (p.Ala46Asn) n.330_331delinsAA | ClinVar dbSNP |
11 | g.32435210del | CA064521 | WT1 | c.151del (p.Ala51ProfsTer?) c.136del (p.Ala46ProfsTer?) n.330del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435210C>A | CA379966279 | WT1 | c.151G>T (p.Ala51Ser) c.136G>T (p.Ala46Ser) n.330G>T | gnomAD v4 |
11 | g.32435210C= | CA1962327395 | WT1 | c.151G= (p.Ala51=) c.136G= (p.Ala46=) n.330G= | |
11 | g.32435210C>G | CA379966277 | WT1 | c.151G>C (p.Ala51Pro) c.136G>C (p.Ala46Pro) n.330G>C | |
11 | g.32435210C>T | CA379966278 | WT1 | c.151G>A (p.Ala51Thr) c.136G>A (p.Ala46Thr) n.330G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435211G>A | CA473773264 | WT1 | c.150C>T (p.Ala50=) c.135C>T (p.Ala45=) n.329C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32435211G>C | CA473773265 | WT1 | c.150C>G (p.Ala50=) c.135C>G (p.Ala45=) n.329C>G | |
11 | g.32435211G= | CA1962327396 | WT1 | c.150C= (p.Ala50=) c.135C= (p.Ala45=) n.329C= | |
11 | g.32435211G>T | CA473773266 | WT1 | c.150C>A (p.Ala50=) c.135C>A (p.Ala45=) n.329C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435212del | CA2499220931 | WT1 | c.150del (p.Ala51ProfsTer?) c.135del (p.Ala46ProfsTer?) n.329del | ClinVar dbSNP |
11 | g.32435212G>A | CA379966280 | WT1 | c.149C>T (p.Ala50Val) c.134C>T (p.Ala45Val) n.328C>T | gnomAD v4 |
11 | g.32435212G>C | CA379966281 | WT1 | c.149C>G (p.Ala50Gly) c.134C>G (p.Ala45Gly) n.328C>G | |
11 | g.32435212G= | CA1962327397 | WT1 | c.149C= (p.Ala50=) c.134C= (p.Ala45=) n.328C= | |
11 | g.32435212G>T | CA219511376 | WT1 | c.149C>A (p.Ala50Asp) c.134C>A (p.Ala45Asp) n.328C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32435214_32435215dup | CA2612989674 | WT1 | c.148_149dup (p.Ala51ProfsTer?) c.133_134dup (p.Ala46ProfsTer?) n.327_328dup | gnomAD v4 |
11 | g.32435213C>A | CA379966282 | WT1 | c.148G>T (p.Ala50Ser) c.133G>T (p.Ala45Ser) n.327G>T | dbSNP gnomAD v4 |
11 | g.32435213C= | CA1962327398 | WT1 | c.148G= (p.Ala50=) c.133G= (p.Ala45=) n.327G= | |
11 | g.32435213C>G | CA379966283 | WT1 | c.148G>C (p.Ala50Pro) c.133G>C (p.Ala45Pro) n.327G>C | dbSNP gnomAD v3 gnomAD v4 |
11 | g.32435213C>T | CA379966284 | WT1 | c.148G>A (p.Ala50Thr) c.133G>A (p.Ala45Thr) n.327G>A | dbSNP gnomAD v4 |
11 | g.32435214G>A | CA473773267 | WT1 | c.147C>T (p.Gly49=) c.132C>T (p.Gly44=) n.326C>T | dbSNP gnomAD v4 |
11 | g.32435214G>C | CA473773268 | WT1 | c.147C>G (p.Gly49=) c.132C>G (p.Gly44=) n.326C>G | dbSNP gnomAD v4 |
11 | g.32435214G>T | CA473773269 | WT1 | c.147C>A (p.Gly49=) c.132C>A (p.Gly44=) n.326C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435215C>A | CA379966285 | WT1 | c.146G>T (p.Gly49Val) c.131G>T (p.Gly44Val) n.325G>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435215C= | CA1962327399 | WT1 | c.146G= (p.Gly49=) c.131G= (p.Gly44=) n.325G= | |
11 | g.32435215C>G | CA379966286 | WT1 | c.146G>C (p.Gly49Ala) c.131G>C (p.Gly44Ala) n.325G>C | |
11 | g.32435215C>T | CA379966287 | WT1 | c.146G>A (p.Gly49Asp) c.131G>A (p.Gly44Asp) n.325G>A | |
11 | g.32435216C>A | CA379966290 | WT1 | c.145G>T (p.Gly49Cys) c.130G>T (p.Gly44Cys) n.324G>T | gnomAD v4 |
11 | g.32435216C= | CA1962327400 | WT1 | c.145G= (p.Gly49=) c.130G= (p.Gly44=) n.324G= | |
11 | g.32435216C>G | CA379966288 | WT1 | c.145G>C (p.Gly49Arg) c.130G>C (p.Gly44Arg) n.324G>C | ClinVar |
11 | g.32435216C>T | CA379966289 | WT1 | c.145G>A (p.Gly49Ser) c.130G>A (p.Gly44Ser) n.324G>A | dbSNP gnomAD v4 |
11 | g.32435217del | CA2612989675 | WT1 | c.144del (p.Gly49AlafsTer?) c.129del (p.Gly44AlafsTer?) n.323del | gnomAD v4 |
11 | g.32435217T>A | CA379966291 | WT1 | c.144A>T (p.Leu48Phe) c.129A>T (p.Leu43Phe) n.323A>T | gnomAD v4 |
11 | g.32435217T>C | CA473773270 | WT1 | c.144A>G (p.Leu48=) c.129A>G (p.Leu43=) n.323A>G | gnomAD v4 |
11 | g.32435217T>G | CA379966292 | WT1 | c.144A>C (p.Leu48Phe) c.129A>C (p.Leu43Phe) n.323A>C | dbSNP |
11 | g.32435217T= | CA1962327401 | WT1 | c.144A= (p.Leu48=) c.129A= (p.Leu43=) n.323A= | |
11 | g.32435218A= | CA1962327402 | WT1 | c.143T= (p.Leu48=) c.128T= (p.Leu43=) n.322T= | |
11 | g.32435218A>C | CA379966293 | WT1 | c.143T>G (p.Leu48Ter) c.128T>G (p.Leu43Ter) n.322T>G | ClinVar |
11 | g.32435218A>G | CA379966294 | WT1 | c.143T>C (p.Leu48Ser) c.128T>C (p.Leu43Ser) n.322T>C | ClinVar dbSNP gnomAD v4 |
11 | g.32435218A>T | CA379966295 | WT1 | c.143T>A (p.Leu48Ter) c.128T>A (p.Leu43Ter) n.322T>A | |
11 | g.32435219del | CA2612989676 | WT1 | c.143del (p.Leu48Ter) c.128del (p.Leu43Ter) n.322del | gnomAD v4 |
11 | g.32435219A= | CA1962327403 | WT1 | c.142T= (p.Leu48=) c.127T= (p.Leu43=) n.321T= | |
11 | g.32435219A>C | CA379966296 | WT1 | c.142T>G (p.Leu48Val) c.127T>G (p.Leu43Val) n.321T>G | gnomAD v4 |
11 | g.32435219A>G | CA219511400 | WT1 | c.142T>C (p.Leu48=) c.127T>C (p.Leu43=) n.321T>C | dbSNP |
11 | g.32435219A>T | CA379966297 | WT1 | c.142T>A (p.Leu48Ile) c.127T>A (p.Leu43Ile) n.321T>A | gnomAD v4 |
11 | g.32435220C>A | CA379966298 | WT1 | c.141G>T (p.Lys47Asn) c.126G>T (p.Lys42Asn) n.320G>T | gnomAD v4 |
11 | g.32435220C= | CA1962327404 | WT1 | c.141G= (p.Lys47=) c.126G= (p.Lys42=) n.320G= | |
11 | g.32435220C>G | CA379966299 | WT1 | c.141G>C (p.Lys47Asn) c.126G>C (p.Lys42Asn) n.320G>C | dbSNP gnomAD v3 gnomAD v4 |
11 | g.32435220C>T | CA473773271 | WT1 | c.141G>A (p.Lys47=) c.126G>A (p.Lys42=) n.320G>A | gnomAD v4 |