Gene >> HOXA13
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000222753 |
| Start |
27199342:27199342(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.736A>G |
| AA Mutation |
p.Met246Val(p.M246V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000222753 |
| Start |
27199614:27199614(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.464C>G |
| AA Mutation |
p.Pro155Arg(p.P155R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |