Gene >> TRIM11
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000284551 |
| Start |
228406227:228406227(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.335C>T |
| AA Mutation |
p.Ala112Val(p.A112V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000284551 |
| Start |
228401003:228401003(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs763571305
|
| CDS Mutation |
c.696C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |