| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000397126 |
| Start |
21972696:21972696(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2338G>A |
| AA Mutation |
p.Glu780Lys(p.E780K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000397126 |
| Start |
21973716:21973716(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1318C>A |
| AA Mutation |
p.Leu440Ile(p.L440I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000397126 |
| Start |
21973828:21973828(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1206T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |