Colon Cancer: Gene >> GTF2H4
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000259895 |
| Start |
30911245:30911245(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.648G>A |
| AA Mutation |
p.Met216Ile(p.M216I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000259895 |
| Start |
30913313:30913313(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1142C>A |
| AA Mutation |
p.Pro381His(p.P381H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> GTF2H4
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000259895 |
| Start |
30911454:30911454(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.696G>T |
| AA Mutation |
p.Glu232Asp(p.E232D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000259895 |
| Start |
30913849:30913849(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1255G>T |
| AA Mutation |
p.Glu419Ter(p.E419*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|