| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000329875 |
| Start |
81936778:81936778(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.37T>G |
| AA Mutation |
p.Phe13Val(p.F13V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000329875 |
| Start |
81935370:81935370(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs113491328
|
| CDS Mutation |
c.285C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000329875 |
| Start |
81936146:81936146(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201218027
|
| CDS Mutation |
c.115C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |