| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000366758 |
| Start |
227734701:227734701(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.516C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000366758 |
| Start |
227733984:227733984(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.615C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> JMJD4
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000366758 |
| Start |
227732508:227732508(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1276G>A |
| AA Mutation |
p.Ala426Thr(p.A426T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000366758 |
| Start |
227732550:227732550(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs748566750
|
| CDS Mutation |
c.1234G>A |
| AA Mutation |
p.Glu412Lys(p.E412K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|