| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000358615 |
| Start |
143876831:143876831(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs763843605
|
| CDS Mutation |
c.161C>T |
| AA Mutation |
p.Ala54Val(p.A54V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000358615 |
| Start |
143905490:143905490(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.18C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> GYPE
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000358615 |
| Start |
143876795:143876795(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.197T>C |
| AA Mutation |
p.Val66Ala(p.V66A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000358615 |
| Start |
143876831:143876831(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs763843605
|
| CDS Mutation |
c.161C>T |
| AA Mutation |
p.Ala54Val(p.A54V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|