Gene >> RGS22
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360863 |
| Start |
100063978:100063978(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.790T>A |
| AA Mutation |
p.Leu264Met(p.L264M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360863 |
| Start |
100040080:100040080(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1946C>A |
| AA Mutation |
p.Thr649Asn(p.T649N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |