| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264220 |
| Start |
56395450:56395450(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1456A>C |
| AA Mutation |
p.Met486Leu(p.M486L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000264220 |
| Start |
56395454:56395454(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1452T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000264220 |
| Start |
56403336:56403336(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs746387194
|
| CDS Mutation |
c.468G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |