| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000233957 |
| Start |
102367840:102367840(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs764661915
|
| CDS Mutation |
c.74G>A |
| AA Mutation |
p.Arg25His(p.R25H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000233957 |
| Start |
102396853:102396853(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1593A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000233957 |
| Start |
102390186:102390186(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1080A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |