Colon Cancer: Gene >> HMGB3
| Mutation ID |
1 |
| Mutation Consequence |
splice_acceptor_variant |
| Transcription ID |
ENST00000325307 |
| Start |
150986050:150986050(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.151-1G>A |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> HMGB3
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000325307 |
| Start |
150985710:150985710(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.111T>G |
| AA Mutation |
p.Asn37Lys(p.N37K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000325307 |
| Start |
150987153:150987153(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.316G>A |
| AA Mutation |
p.Glu106Lys(p.E106K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000325307 |
| Start |
150987797:150987797(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs782588935
|
| CDS Mutation |
c.486G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|