Gene >> NELFCD
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000602795 |
| Start |
58989609:58989609(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.680A>C |
| AA Mutation |
p.Glu227Ala(p.E227A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000602795 |
| Start |
58994668:58994668(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1792G>T |
| AA Mutation |
p.Val598Leu(p.V598L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |