| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000338448 |
| Start |
736048:736048(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.472A>G |
| AA Mutation |
p.Thr158Ala(p.T158A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000338448 |
| Start |
746652:746652(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs753694815
|
| CDS Mutation |
c.1002G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000338448 |
| Start |
746586:746586(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs142619819
|
| CDS Mutation |
c.936C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |