| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000295981 |
| Start |
9920537:9920537(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.725T>C |
| AA Mutation |
p.Val242Ala(p.V242A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000295981 |
| Start |
9928336:9928336(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs370054868
|
| CDS Mutation |
c.1122C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000295981 |
| Start |
9933473:9933473(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs762979312
|
| CDS Mutation |
c.2256G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |