Gene >> CD38
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000226279 |
| Start |
15816566:15816566(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.289C>A |
| AA Mutation |
p.His97Asn(p.H97N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000226279 |
| Start |
15778611:15778611(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.197G>C |
| AA Mutation |
p.Arg66Pro(p.R66P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |