| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000423302 |
| Start |
10581880:10581880(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2347G>A |
| AA Mutation |
p.Ala783Thr(p.A783T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000423302 |
| Start |
10623848:10623848(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1377C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000423302 |
| Start |
10576340:10576340(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2731G>T |
| AA Mutation |
p.Glu911Ter(p.E911*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |