Gene >> MEF2D
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000348159 |
| Start |
156482586:156482586(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.109G>A |
| AA Mutation |
p.Val37Met(p.V37M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000348159 |
| Start |
156468863:156468863(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1164G>T |
| AA Mutation |
p.Gln388His(p.Q388H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |