| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000305218 |
| Start |
64194210:64194210(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.241G>A |
| AA Mutation |
p.Ala81Thr(p.A81T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000305218 |
| Start |
64203578:64203578(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1515C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000305218 |
| Start |
64203153:64203153(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs2070232
|
| CDS Mutation |
c.1311G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |