| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000280326 |
| Start |
10261649:10261649(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1083G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
7 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000280326 |
| Start |
10258502:10258502(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.840C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
8 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000280326 |
| Start |
10264703:10264703(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1546C>T |
| AA Mutation |
p.Gln516Ter(p.Q516*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |