| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000221930 |
| Start |
41352959:41352959(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs199758510
|
| CDS Mutation |
c.86G>A |
| AA Mutation |
p.Gly29Glu(p.G29E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000221930 |
| Start |
41344810:41344810(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201383660
|
| CDS Mutation |
c.571G>A |
| AA Mutation |
p.Asp191Asn(p.D191N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000221930 |
| Start |
41344766:41344766(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.615G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |