| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000329342 |
| Start |
152767568:152767568(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.83C>T |
| AA Mutation |
p.Ala28Val(p.A28V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000329342 |
| Start |
152766953:152766953(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.698G>T |
| AA Mutation |
p.Gly233Val(p.G233V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000329342 |
| Start |
152767363:152767363(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.288C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |