| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360323 |
| Start |
29829858:29829858(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.938C>T |
| AA Mutation |
p.Ala313Val(p.A313V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360323 |
| Start |
29829502:29829502(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs147620137
|
| CDS Mutation |
c.704C>T |
| AA Mutation |
p.Ala235Val(p.A235V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000360323 |
| Start |
29828186:29828186(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.213G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |