Colon Cancer: Gene >> VAMP8
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263864 |
| Start |
85579073:85579073(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.68T>A |
| AA Mutation |
p.Val23Asp(p.V23D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263864 |
| Start |
85581699:85581699(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.286A>G |
| AA Mutation |
p.Thr96Ala(p.T96A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> VAMP8
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263864 |
| Start |
85579131:85579131(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.126A>C |
| AA Mutation |
p.Glu42Asp(p.E42D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263864 |
| Start |
85581646:85581646(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.233T>C |
| AA Mutation |
p.Val78Ala(p.V78A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|