Gene >> RASGRF2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265080 |
| Start |
81080645:81080645(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1017T>G |
| AA Mutation |
p.Phe339Leu(p.F339L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265080 |
| Start |
81109008:81109008(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1768A>G |
| AA Mutation |
p.Ile590Val(p.I590V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |