Colon Cancer: Gene >> OVOL2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000278780 |
| Start |
18041638:18041638(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs368800012
|
| CDS Mutation |
c.407G>A |
| AA Mutation |
p.Arg136His(p.R136H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000278780 |
| Start |
18024807:18024807(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs772646157
|
| CDS Mutation |
c.657C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> OVOL2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000278780 |
| Start |
18024763:18024763(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.701A>G |
| AA Mutation |
p.Asn234Ser(p.N234S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000278780 |
| Start |
18056678:18056678(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.300G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|