| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000534062 |
| Start |
100884006:100884006(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.783C>A |
| AA Mutation |
p.Ser261Arg(p.S261R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000534062 |
| Start |
100882873:100882873(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1916T>G |
| AA Mutation |
p.Met639Arg(p.M639R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000534062 |
| Start |
100882413:100882413(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2376C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |