| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000280377 |
| Start |
62383957:62383957(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1207C>T |
| AA Mutation |
p.Pro403Ser(p.P403S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000280377 |
| Start |
62381603:62381603(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1029C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000280377 |
| Start |
62321546:62321546(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.558C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |