| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000199936 |
| Start |
82071101:82071101(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.638G>T |
| AA Mutation |
p.Arg213Met(p.R213M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000199936 |
| Start |
82098232:82098232(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs780429754
|
| CDS Mutation |
c.960G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000199936 |
| Start |
82098301:82098301(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs779441409
|
| CDS Mutation |
c.1029C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |