Colon Cancer: Gene >> PDCD1LG2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000397747 |
| Start |
5549550:5549550(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.577G>A |
| AA Mutation |
p.Val193Met(p.V193M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000397747 |
| Start |
5534804:5534804(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.115A>T |
| AA Mutation |
p.Thr39Ser(p.T39S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> PDCD1LG2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000397747 |
| Start |
5563200:5563200(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.805G>A |
| AA Mutation |
p.Val269Met(p.V269M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|