Gene >> S1PR5
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000333430 |
| Start |
10514444:10514444(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs777770115
|
| CDS Mutation |
c.568G>A |
| AA Mutation |
p.Ala190Thr(p.A190T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000333430 |
| Start |
10513923:10513923(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1089G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |