Gene >> GPRIN2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000374314 |
| Start |
46549544:46549544(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1193T>C |
| AA Mutation |
p.Val398Ala(p.V398A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000374314 |
| Start |
46549949:46549949(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.788C>T |
| AA Mutation |
p.Ala263Val(p.A263V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |