| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000216281 |
| Start |
102081789:102081789(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2122A>G |
| AA Mutation |
p.Thr708Ala(p.T708A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000216281 |
| Start |
102083627:102083627(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1405G>A |
| AA Mutation |
p.Ala469Thr(p.A469T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000216281 |
| Start |
102086005:102086005(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.282T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |