| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371506 |
| Start |
137437002:137437002(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.422A>G |
| AA Mutation |
p.Asp141Gly(p.D141G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000371506 |
| Start |
137435031:137435031(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs140934866
|
| CDS Mutation |
c.1371G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000371506 |
| Start |
137436160:137436160(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.903C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |