| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000406386 |
| Start |
37769355:37769355(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs765348097
|
| CDS Mutation |
c.6829C>T |
| AA Mutation |
p.Arg2277Trp(p.R2277W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000406386 |
| Start |
37723244:37723244(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.688G>A |
| AA Mutation |
p.Gly230Arg(p.G230R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000406386 |
| Start |
37769056:37769056(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs769873790
|
| CDS Mutation |
c.6604C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |