Gene >> RGS22
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360863 |
| Start |
100062723:100062723(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1382T>C |
| AA Mutation |
p.Leu461Pro(p.L461P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000360863 |
| Start |
100006056:100006056(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2415A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |