| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357402 |
| Start |
29844815:29844815(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1957G>A |
| AA Mutation |
p.Ala653Thr(p.A653T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000357402 |
| Start |
29846191:29846191(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs749354165
|
| CDS Mutation |
c.2172G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000357402 |
| Start |
29844583:29844583(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs372666702
|
| CDS Mutation |
c.1725C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |