| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302068 |
| Start |
154570579:154570579(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1405A>C |
| AA Mutation |
p.Asn469His(p.N469H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302068 |
| Start |
154567646:154567646(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.544T>C |
| AA Mutation |
p.Tyr182His(p.Y182H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000302068 |
| Start |
154566608:154566608(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.426T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |