Gene >> FPR2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000340023 |
| Start |
51768995:51768995(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.337G>A |
| AA Mutation |
p.Val113Ile(p.V113I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000340023 |
| Start |
51768996:51768996(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.338T>C |
| AA Mutation |
p.Val113Ala(p.V113A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |