| Mutation ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000287600 |
| Start |
231737282:231737282(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs571686278
|
| CDS Mutation |
c.276C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
5 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000287600 |
| Start |
231737243:231737243(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.315G>A |
| AA Mutation |
p.Trp105Ter(p.W105*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> PDE6D
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000287600 |
| Start |
231738120:231738120(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.158T>A |
| AA Mutation |
p.Ile53Asn(p.I53N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|