| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000229708 |
| Start |
149969213:149969213(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs769275822
|
| CDS Mutation |
c.478G>A |
| AA Mutation |
p.Ala160Thr(p.A160T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000229708 |
| Start |
149969335:149969335(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.600C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000229708 |
| Start |
149969144:149969144(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.409G>T |
| AA Mutation |
p.Gly137Ter(p.G137*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |