Gene >> KAT8
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000219797 |
| Start |
31120405:31120405(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.353C>T |
| AA Mutation |
p.Ala118Val(p.A118V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000219797 |
| Start |
31117691:31117691(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.10C>G |
| AA Mutation |
p.Gln4Glu(p.Q4E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |