Gene >> TOP2A
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000423485 |
| Start |
40398880:40398880(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3346G>A |
| AA Mutation |
p.Asp1116Asn(p.D1116N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000423485 |
| Start |
40408529:40408529(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1305C>G |
| AA Mutation |
p.Ile435Met(p.I435M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |