| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000279022 |
| Start |
36548125:36548125(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.278A>C |
| AA Mutation |
p.Lys93Thr(p.K93T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000279022 |
| Start |
36549164:36549164(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.434A>G |
| AA Mutation |
p.Glu145Gly(p.E145G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000279022 |
| Start |
36548072:36548072(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs368093790
|
| CDS Mutation |
c.225C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |