Gene >> CD36
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000309881 |
| Start |
80666465:80666465(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.724C>G |
| AA Mutation |
p.His242Asp(p.H242D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000309881 |
| Start |
80646816:80646816(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.76C>G |
| AA Mutation |
p.Leu26Val(p.L26V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |