Gene >> RPN2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000237530 |
| Start |
37199099:37199099(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.353A>T |
| AA Mutation |
p.Glu118Val(p.E118V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000237530 |
| Start |
37236596:37236596(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1770G>T |
| AA Mutation |
p.Met590Ile(p.M590I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |