| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264360 |
| Start |
133154361:133154361(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2686A>C |
| AA Mutation |
p.Asn896His(p.N896H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264360 |
| Start |
133150565:133150565(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.425C>A |
| AA Mutation |
p.Pro142His(p.P142H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000264360 |
| Start |
133163110:133163110(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2931C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |