| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000324333 |
| Start |
3829351:3829351(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs772874731
|
| CDS Mutation |
c.2150A>G |
| AA Mutation |
p.Asp717Gly(p.D717G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000324333 |
| Start |
4118509:4118509(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201431173
|
| CDS Mutation |
c.504G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000381971 |
| Start |
4286138:4286138(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs371790247
|
| CDS Mutation |
c.288G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |