| Mutation ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265753 |
| Start |
74189692:74189692(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs575887795
|
| CDS Mutation |
c.267C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
6 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000265753 |
| Start |
74187800:74187800(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.247+2T>C |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> EIF4H
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265753 |
| Start |
74195208:74195208(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.647G>A |
| AA Mutation |
p.Arg216Gln(p.R216Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|