| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000369130 |
| Start |
150082876:150082876(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs782085785
|
| CDS Mutation |
c.1097C>T |
| AA Mutation |
p.Ala366Val(p.A366V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000369130 |
| Start |
150081953:150081953(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.892A>G |
| AA Mutation |
p.Lys298Glu(p.K298E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000369130 |
| Start |
150081410:150081410(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs375831361
|
| CDS Mutation |
c.756G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |