| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000379906 |
| Start |
55702334:55702334(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1842G>T |
| AA Mutation |
p.Trp614Cys(p.W614C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000379906 |
| Start |
55691989:55691989(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs180935423
|
| CDS Mutation |
c.855C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000379906 |
| Start |
55692001:55692001(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.867T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |