| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000273371 |
| Start |
119616059:119616059(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs372028931
|
| CDS Mutation |
c.712G>A |
| AA Mutation |
p.Gly238Arg(p.G238R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000273371 |
| Start |
119606805:119606805(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs753943074
|
| CDS Mutation |
c.105C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000273371 |
| Start |
119606877:119606877(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.177G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |