| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000247584 |
| Start |
41582894:41582894(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1904G>A |
| AA Mutation |
p.Gly635Asp(p.G635D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000247584 |
| Start |
41580439:41580439(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4359G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000247584 |
| Start |
41524898:41524898(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.5220C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |