| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000393980 |
| Start |
160199128:160199128(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.22A>G |
| AA Mutation |
p.Met8Val(p.M8V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000402432 |
| Start |
160232141:160232141(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs762811726
|
| CDS Mutation |
c.111C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> FABP6
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000402432 |
| Start |
160232141:160232141(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs762811726
|
| CDS Mutation |
c.111C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|