| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000318247 |
| Start |
151816684:151816684(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs546157871
|
| CDS Mutation |
c.278C>T |
| AA Mutation |
p.Ala93Val(p.A93V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000318247 |
| Start |
151813267:151813267(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs752324102
|
| CDS Mutation |
c.1146C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000318247 |
| Start |
151815415:151815415(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs267598021
|
| CDS Mutation |
c.309C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |