| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000370060 |
| Start |
153868862:153868862(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1358C>T |
| AA Mutation |
p.Ala453Val(p.A453V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000370060 |
| Start |
153865332:153865332(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs782505398
|
| CDS Mutation |
c.2716G>A |
| AA Mutation |
p.Ala906Thr(p.A906T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000370060 |
| Start |
153868631:153868631(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs150805225
|
| CDS Mutation |
c.1476C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |