Gene >> SLC39A6
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000269187 |
| Start |
36126802:36126802(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs749354395
|
| CDS Mutation |
c.206C>A |
| AA Mutation |
p.Ser69Tyr(p.S69Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000269187 |
| Start |
36112546:36112546(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1879A>G |
| AA Mutation |
p.Ser627Gly(p.S627G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |