| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000236147 |
| Start |
169708444:169708444(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.484A>G |
| AA Mutation |
p.Lys162Glu(p.K162E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000236147 |
| Start |
169708694:169708694(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.234T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000236147 |
| Start |
169707434:169707434(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.527G>A |
| AA Mutation |
p.Trp176Ter(p.W176*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |