Colon Cancer: Gene >> POMP
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000380842 |
| Start |
28678048:28678048(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs368820757
|
| CDS Mutation |
c.372C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> POMP
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380842 |
| Start |
28664519:28664519(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs148838797
|
| CDS Mutation |
c.112G>C |
| AA Mutation |
p.Val38Leu(p.V38L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380842 |
| Start |
28678049:28678049(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.373G>A |
| AA Mutation |
p.Glu125Lys(p.E125K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|