Colon Cancer: Gene >> CLDN2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000336803 |
| Start |
106928776:106928776(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.548T>A |
| AA Mutation |
p.Phe183Tyr(p.F183Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000336803 |
| Start |
106928865:106928865(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.637C>T |
| AA Mutation |
p.Gln213Ter(p.Q213*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CLDN2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000336803 |
| Start |
106928443:106928443(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.215G>A |
| AA Mutation |
p.Gly72Asp(p.G72D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|