UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.32428498_32428620del | CA645577714 | WT1 | c.664_784+2del c.13_133+2del c.40_160+2del c.649_769+2del c.-99_22+2del n.843_963+2del | COSMIC |
| 11 | g.32428500G>A | CA473570146 | WT1 | c.781C>T (p.Leu261=) c.130C>T (p.Leu44=) c.157C>T (p.Leu53=) c.766C>T (p.Leu256=) c.19C>T (p.Leu7=) n.960C>T | dbSNP |
| 11 | g.32428500G>C | CA379963257 | WT1 | c.781C>G (p.Leu261Val) c.130C>G (p.Leu44Val) c.157C>G (p.Leu53Val) c.766C>G (p.Leu256Val) c.19C>G (p.Leu7Val) n.960C>G | ClinVar |
| 11 | g.32428500G= | CA1962323546 | WT1 | c.781C= (p.Leu261=) c.130C= (p.Leu44=) c.157C= (p.Leu53=) c.766C= (p.Leu256=) c.19C= (p.Leu7=) n.960C= | |
| 11 | g.32428500G>T | CA379963258 | WT1 | c.781C>A (p.Leu261Met) c.130C>A (p.Leu44Met) c.157C>A (p.Leu53Met) c.766C>A (p.Leu256Met) c.19C>A (p.Leu7Met) n.960C>A | |
| 11 | g.32428500_32428505delinsTCGGGTAGGGG | CA645577717 | WT1 | c.776_781delinsCCCCTACCCGA (p.Gly259AlafsTer34) c.125_130delinsCCCCTACCCGA (p.Gly42AlafsTer34) c.152_157delinsCCCCTACCCGA (p.Gly51AlafsTer34) c.761_766delinsCCCCTACCCGA (p.Gly254AlafsTer34) c.14_19delinsCCCCTACCCGA (p.Gly5AlafsTer34) n.955_960delinsCCCCTACCCGA | COSMIC |
| 11 | g.32428501C>A | CA473570149 | WT1 | c.780G>T (p.Ser260=) c.129G>T (p.Ser43=) c.156G>T (p.Ser52=) c.765G>T (p.Ser255=) c.18G>T (p.Ser6=) n.959G>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.32428501C= | CA1962323547 | WT1 | c.780G= (p.Ser260=) c.129G= (p.Ser43=) c.156G= (p.Ser52=) c.765G= (p.Ser255=) c.18G= (p.Ser6=) n.959G= | |
| 11 | g.32428501C>G | CA473570150 | WT1 | c.780G>C (p.Ser260=) c.129G>C (p.Ser43=) c.156G>C (p.Ser52=) c.765G>C (p.Ser255=) c.18G>C (p.Ser6=) n.959G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.32428501C>T | CA473570151 | WT1 | c.780G>A (p.Ser260=) c.129G>A (p.Ser43=) c.156G>A (p.Ser52=) c.765G>A (p.Ser255=) c.18G>A (p.Ser6=) n.959G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.32428502G>A | CA379963259 | WT1 | c.779C>T (p.Ser260Leu) c.128C>T (p.Ser43Leu) c.155C>T (p.Ser52Leu) c.764C>T (p.Ser255Leu) c.17C>T (p.Ser6Leu) n.958C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.32428502G>C | CA379963260 | WT1 | c.779C>G (p.Ser260Trp) c.128C>G (p.Ser43Trp) c.155C>G (p.Ser52Trp) c.764C>G (p.Ser255Trp) c.17C>G (p.Ser6Trp) n.958C>G | |
| 11 | g.32428502G= | CA1962323548 | WT1 | c.779C= (p.Ser260=) c.128C= (p.Ser43=) c.155C= (p.Ser52=) c.764C= (p.Ser255=) c.17C= (p.Ser6=) n.958C= | |
| 11 | g.32428502G>T | CA379963261 | WT1 | c.779C>A (p.Ser260Ter) c.128C>A (p.Ser43Ter) c.155C>A (p.Ser52Ter) c.764C>A (p.Ser255Ter) c.17C>A (p.Ser6Ter) n.958C>A | COSMIC |
| 11 | g.32428503A>C | CA379963262 | WT1 | c.778T>G (p.Ser260Ala) c.127T>G (p.Ser43Ala) c.154T>G (p.Ser52Ala) c.763T>G (p.Ser255Ala) c.16T>G (p.Ser6Ala) n.957T>G | |
| 11 | g.32428503A>G | CA379963263 | WT1 | c.778T>C (p.Ser260Pro) c.127T>C (p.Ser43Pro) c.154T>C (p.Ser52Pro) c.763T>C (p.Ser255Pro) c.16T>C (p.Ser6Pro) n.957T>C | |
| 11 | g.32428503A>T | CA379963264 | WT1 | c.778T>A (p.Ser260Thr) c.127T>A (p.Ser43Thr) c.154T>A (p.Ser52Thr) c.763T>A (p.Ser255Thr) c.16T>A (p.Ser6Thr) n.957T>A | COSMIC COSMIC COSMIC |
| 11 | g.32428504G>A | CA473570159 | WT1 | c.777C>T (p.Gly259=) c.126C>T (p.Gly42=) c.153C>T (p.Gly51=) c.762C>T (p.Gly254=) c.15C>T (p.Gly5=) n.956C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.32428504G>C | CA473570163 | WT1 | c.777C>G (p.Gly259=) c.126C>G (p.Gly42=) c.153C>G (p.Gly51=) c.762C>G (p.Gly254=) c.15C>G (p.Gly5=) n.956C>G | |
| 11 | g.32428504G= | CA1962323549 | WT1 | c.777C= (p.Gly259=) c.126C= (p.Gly42=) c.153C= (p.Gly51=) c.762C= (p.Gly254=) c.15C= (p.Gly5=) n.956C= | |
| 11 | g.32428504G>T | CA473570161 | WT1 | c.777C>A (p.Gly259=) c.126C>A (p.Gly42=) c.153C>A (p.Gly51=) c.762C>A (p.Gly254=) c.15C>A (p.Gly5=) n.956C>A | ClinVar dbSNP |
| 11 | g.32428505C>A | CA379963265 | WT1 | c.776G>T (p.Gly259Val) c.125G>T (p.Gly42Val) c.152G>T (p.Gly51Val) c.761G>T (p.Gly254Val) c.14G>T (p.Gly5Val) n.955G>T | dbSNP |
| 11 | g.32428505C= | CA1962323550 | WT1 | c.776G= (p.Gly259=) c.125G= (p.Gly42=) c.152G= (p.Gly51=) c.761G= (p.Gly254=) c.14G= (p.Gly5=) n.955G= | |
| 11 | g.32428505C>G | CA379963266 | WT1 | c.776G>C (p.Gly259Ala) c.125G>C (p.Gly42Ala) c.152G>C (p.Gly51Ala) c.761G>C (p.Gly254Ala) c.14G>C (p.Gly5Ala) n.955G>C | |
| 11 | g.32428505C>T | CA379963267 | WT1 | c.776G>A (p.Gly259Asp) c.125G>A (p.Gly42Asp) c.152G>A (p.Gly51Asp) c.761G>A (p.Gly254Asp) c.14G>A (p.Gly5Asp) n.955G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.32428506C>A | CA379963268 | WT1 | c.775G>T (p.Gly259Cys) c.124G>T (p.Gly42Cys) c.151G>T (p.Gly51Cys) c.760G>T (p.Gly254Cys) c.13G>T (p.Gly5Cys) n.954G>T | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.32428506C= | CA1962323551 | WT1 | c.775G= (p.Gly259=) c.124G= (p.Gly42=) c.151G= (p.Gly51=) c.760G= (p.Gly254=) c.13G= (p.Gly5=) n.954G= | |
| 11 | g.32428506C>G | CA379963269 | WT1 | c.775G>C (p.Gly259Arg) c.124G>C (p.Gly42Arg) c.151G>C (p.Gly51Arg) c.760G>C (p.Gly254Arg) c.13G>C (p.Gly5Arg) n.954G>C | COSMIC COSMIC |
| 11 | g.32428506C>T | CA379963270 | WT1 | c.775G>A (p.Gly259Ser) c.124G>A (p.Gly42Ser) c.151G>A (p.Gly51Ser) c.760G>A (p.Gly254Ser) c.13G>A (p.Gly5Ser) n.954G>A | |
| 11 | g.32428506_32428509delinsCCTG | CA1962323552 | WT1 | c.772_775delinsCAGG (p.Gln258=) c.121_124delinsCAGG (p.Gln41=) c.148_151delinsCAGG (p.Gln50=) c.757_760delinsCAGG (p.Gln253=) c.10_13delinsCAGG (p.Gln4=) n.951_954delinsCAGG | |
| 11 | g.32428507C>A | CA379963271 | WT1 | c.774G>T (p.Gln258His) c.123G>T (p.Gln41His) c.150G>T (p.Gln50His) c.759G>T (p.Gln253His) c.12G>T (p.Gln4His) n.953G>T | |
| 11 | g.32428507C= | CA1962323554 | WT1 | c.774G= (p.Gln258=) c.123G= (p.Gln41=) c.150G= (p.Gln50=) c.759G= (p.Gln253=) c.12G= (p.Gln4=) n.953G= | |
| 11 | g.32428507C>G | CA379963272 | WT1 | c.774G>C (p.Gln258His) c.123G>C (p.Gln41His) c.150G>C (p.Gln50His) c.759G>C (p.Gln253His) c.12G>C (p.Gln4His) n.953G>C | ClinVar dbSNP |
| 11 | g.32428507C>T | CA473570170 | WT1 | c.774G>A (p.Gln258=) c.123G>A (p.Gln41=) c.150G>A (p.Gln50=) c.759G>A (p.Gln253=) c.12G>A (p.Gln4=) n.953G>A | ClinVar |
| 11 | g.32428510_32428512del | CA1962323553 | WT1 | c.772_774del (p.Gln258del) c.121_123del (p.Gln41del) c.148_150del (p.Gln50del) c.757_759del (p.Gln253del) c.10_12del (p.Gln4del) n.951_953del | dbSNP |
| 11 | g.32428508T>A | CA379963273 | WT1 | c.773A>T (p.Gln258Leu) c.122A>T (p.Gln41Leu) c.149A>T (p.Gln50Leu) c.758A>T (p.Gln253Leu) c.11A>T (p.Gln4Leu) n.952A>T | |
| 11 | g.32428508T>C | CA379963274 | WT1 | c.773A>G (p.Gln258Arg) c.122A>G (p.Gln41Arg) c.149A>G (p.Gln50Arg) c.758A>G (p.Gln253Arg) c.11A>G (p.Gln4Arg) n.952A>G | ClinVar dbSNP |
| 11 | g.32428508T>G | CA379963275 | WT1 | c.773A>C (p.Gln258Pro) c.122A>C (p.Gln41Pro) c.149A>C (p.Gln50Pro) c.758A>C (p.Gln253Pro) c.11A>C (p.Gln4Pro) n.952A>C | |
| 11 | g.32428508T= | CA1962323555 | WT1 | c.773A= (p.Gln258=) c.122A= (p.Gln41=) c.149A= (p.Gln50=) c.758A= (p.Gln253=) c.11A= (p.Gln4=) n.952A= | |
| 11 | g.32428509G>A | CA379963276 | WT1 | c.772C>T (p.Gln258Ter) c.121C>T (p.Gln41Ter) c.148C>T (p.Gln50Ter) c.757C>T (p.Gln253Ter) c.10C>T (p.Gln4Ter) n.951C>T | dbSNP COSMIC |
| 11 | g.32428509G>C | CA379963277 | WT1 | c.772C>G (p.Gln258Glu) c.121C>G (p.Gln41Glu) c.148C>G (p.Gln50Glu) c.757C>G (p.Gln253Glu) c.10C>G (p.Gln4Glu) n.951C>G | |
| 11 | g.32428509G>T | CA379963278 | WT1 | c.772C>A (p.Gln258Lys) c.121C>A (p.Gln41Lys) c.148C>A (p.Gln50Lys) c.757C>A (p.Gln253Lys) c.10C>A (p.Gln4Lys) n.951C>A | gnomAD v4 |
| 11 | g.32428510C>A | CA379963279 | WT1 | c.771G>T (p.Gln257His) c.120G>T (p.Gln40His) c.147G>T (p.Gln49His) c.756G>T (p.Gln252His) c.9G>T (p.Gln3His) n.950G>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.32428510C= | CA1962323556 | WT1 | c.771G= (p.Gln257=) c.120G= (p.Gln40=) c.147G= (p.Gln49=) c.756G= (p.Gln252=) c.9G= (p.Gln3=) n.950G= | |
| 11 | g.32428510C>G | CA379963280 | WT1 | c.771G>C (p.Gln257His) c.120G>C (p.Gln40His) c.147G>C (p.Gln49His) c.756G>C (p.Gln252His) c.9G>C (p.Gln3His) n.950G>C | |
| 11 | g.32428510C>T | CA473570179 | WT1 | c.771G>A (p.Gln257=) c.120G>A (p.Gln40=) c.147G>A (p.Gln49=) c.756G>A (p.Gln252=) c.9G>A (p.Gln3=) n.950G>A | ClinVar dbSNP |
| 11 | g.32428511T>A | CA379963281 | WT1 | c.770A>T (p.Gln257Leu) c.119A>T (p.Gln40Leu) c.146A>T (p.Gln49Leu) c.755A>T (p.Gln252Leu) c.8A>T (p.Gln3Leu) n.949A>T | |
| 11 | g.32428511T>C | CA379963282 | WT1 | c.770A>G (p.Gln257Arg) c.119A>G (p.Gln40Arg) c.146A>G (p.Gln49Arg) c.755A>G (p.Gln252Arg) c.8A>G (p.Gln3Arg) n.949A>G | |
| 11 | g.32428511T>G | CA379963283 | WT1 | c.770A>C (p.Gln257Pro) c.119A>C (p.Gln40Pro) c.146A>C (p.Gln49Pro) c.755A>C (p.Gln252Pro) c.8A>C (p.Gln3Pro) n.949A>C | |
| 11 | g.32428511dup | CA2695213421 | WT1 | c.770dup (p.Gln258AlafsTer6) c.119dup (p.Gln41AlafsTer6) c.146dup (p.Gln50AlafsTer6) c.755dup (p.Gln253AlafsTer6) c.8dup (p.Gln4AlafsTer6) n.949dup |