Gene >> SGCG
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000218867 |
| Start |
23234630:23234630(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.215G>T |
| AA Mutation |
p.Cys72Phe(p.C72F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000218867 |
| Start |
23279467:23279467(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.494T>G |
| AA Mutation |
p.Leu165Arg(p.L165R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |