Gene >> SLC18A2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000298472 |
| Start |
117244169:117244169(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.320T>C |
| AA Mutation |
p.Val107Ala(p.V107A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000298472 |
| Start |
117241712:117241712(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.19G>C |
| AA Mutation |
p.Ala7Pro(p.A7P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |