| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000358465 |
| Start |
114425598:114425598(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1546C>A |
| AA Mutation |
p.Leu516Ile(p.L516I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000358465 |
| Start |
114405566:114405566(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs752539788
|
| CDS Mutation |
c.2612C>T |
| AA Mutation |
p.Ser871Leu(p.S871L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000358465 |
| Start |
114425605:114425605(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1539G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |