| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000257192 |
| Start |
31336505:31336505(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs557916314
|
| CDS Mutation |
c.1157G>A |
| AA Mutation |
p.Arg386His(p.R386H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000257192 |
| Start |
31355076:31355076(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs200560952
|
| CDS Mutation |
c.2880C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000257192 |
| Start |
31354644:31354644(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs772943379
|
| CDS Mutation |
c.2448G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |