| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000389232 |
| Start |
33739847:33739847(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.7672C>G |
| AA Mutation |
p.Leu2558Val(p.L2558V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000389232 |
| Start |
33581534:33581534(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1464C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000389232 |
| Start |
33726488:33726488(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.7015C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |