| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000402038 |
| Start |
49820197:49820197(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2744A>G |
| AA Mutation |
p.His915Arg(p.H915R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000402038 |
| Start |
49819372:49819372(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2899G>T |
| AA Mutation |
p.Ala967Ser(p.A967S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000402038 |
| Start |
49820172:49820172(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2769C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |