Gene >> PEG10
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000482108 |
| Start |
94664184:94664184(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.628C>T |
| AA Mutation |
p.Leu210Phe(p.L210F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000482108 |
| Start |
94664062:94664062(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.506G>A |
| AA Mutation |
p.Arg169His(p.R169H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |