| Mutation ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000417257 |
| Start |
43883748:43883748(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs371269803
|
| CDS Mutation |
c.1090G>A |
| AA Mutation |
p.Val364Ile(p.V364I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
6 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000417257 |
| Start |
43892023:43892023(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.686T>G |
| AA Mutation |
p.Phe229Cys(p.F229C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> FRMD5
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000417257 |
| Start |
43874130:43874130(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs551307319
|
| CDS Mutation |
c.1468G>A |
| AA Mutation |
p.Glu490Lys(p.E490K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|