| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000389362 |
| Start |
11393445:11393445(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs751356932
|
| CDS Mutation |
c.633A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000389362 |
| Start |
11393442:11393442(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs557500313
|
| CDS Mutation |
c.636T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000389362 |
| Start |
11393708:11393708(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.370C>T |
| AA Mutation |
p.Gln124Ter(p.Q124*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |