| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000376296 |
| Start |
30987488:30987488(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1313C>G |
| AA Mutation |
p.Ser438Cys(p.S438C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000376296 |
| Start |
30987549:30987549(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1374T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000376296 |
| Start |
30986850:30986850(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs755308293
|
| CDS Mutation |
c.675C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |