| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000286692 |
| Start |
111120651:111120651(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.382A>G |
| AA Mutation |
p.Thr128Ala(p.T128A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000286692 |
| Start |
111118814:111118814(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.684T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000286692 |
| Start |
111124829:111124829(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.252A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |