Gene >> SLC7A8
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000316902 |
| Start |
23182833:23182833(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.82G>C |
| AA Mutation |
p.Gly28Arg(p.G28R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000316902 |
| Start |
23166536:23166536(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.156C>G |
| AA Mutation |
p.Asn52Lys(p.N52K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |