Colon Cancer: Gene >> TAGLN
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000278968 |
| Start |
117203050:117203050(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs774227686
|
| CDS Mutation |
c.37G>A |
| AA Mutation |
p.Glu13Lys(p.E13K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000278968 |
| Start |
117204220:117204220(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs138736412
|
| CDS Mutation |
c.467C>T |
| AA Mutation |
p.Ala156Val(p.A156V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> TAGLN
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000278968 |
| Start |
117203353:117203353(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs780383343
|
| CDS Mutation |
c.227C>T |
| AA Mutation |
p.Pro76Leu(p.P76L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000278968 |
| Start |
117203083:117203083(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs746670728
|
| CDS Mutation |
c.70G>A |
| AA Mutation |
p.Glu24Lys(p.E24K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|