| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000614565 |
| Start |
61743631:61743631(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.238G>T |
| AA Mutation |
p.Gly80Trp(p.G80W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000614565 |
| Start |
61743599:61743599(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs182629710
|
| CDS Mutation |
c.206A>G |
| AA Mutation |
p.Gln69Arg(p.Q69R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000614565 |
| Start |
61773032:61773032(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.426G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |