| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000316099 |
| Start |
44414540:44414540(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.526A>C |
| AA Mutation |
p.Ile176Leu(p.I176L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000316099 |
| Start |
44429590:44429590(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs377052026
|
| CDS Mutation |
c.1350G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000316099 |
| Start |
44428441:44428441(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1236C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |