| Mutation ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000337147 |
| Start |
158769872:158769872(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs571220845
|
| CDS Mutation |
c.1163G>A |
| AA Mutation |
p.Arg388His(p.R388H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000337147 |
| Start |
158767075:158767075(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1600C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> EZR
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000337147 |
| Start |
158769815:158769815(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1220C>T |
| AA Mutation |
p.Ala407Val(p.A407V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|