Colon Cancer: Gene >> CPA2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000222481 |
| Start |
130273153:130273153(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.462G>T |
| AA Mutation |
p.Glu154Asp(p.E154D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000222481 |
| Start |
130269701:130269701(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.186G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CPA2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000222481 |
| Start |
130289644:130289644(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs146602328
|
| CDS Mutation |
c.1157G>A |
| AA Mutation |
p.Arg386His(p.R386H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000222481 |
| Start |
130277847:130277847(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs145958174
|
| CDS Mutation |
c.718C>T |
| AA Mutation |
p.Arg240Trp(p.R240W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|