| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000284984 |
| Start |
26844683:26844683(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.272C>A |
| AA Mutation |
p.Pro91His(p.P91H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000284984 |
| Start |
26838227:26838227(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2256A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000284984 |
| Start |
26838209:26838209(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2274G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |