| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000220062 |
| Start |
65058494:65058494(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs142747328
|
| CDS Mutation |
c.358G>A |
| AA Mutation |
p.Ala120Thr(p.A120T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000220062 |
| Start |
65058596:65058596(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs138898900
|
| CDS Mutation |
c.256C>T |
| AA Mutation |
p.Arg86Cys(p.R86C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> RASL12
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000220062 |
| Start |
65054973:65054973(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs553620483
|
| CDS Mutation |
c.727G>A |
| AA Mutation |
p.Val243Met(p.V243M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|