Gene >> GEMIN4
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000319004 |
| Start |
746557:746557(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1486A>C |
| AA Mutation |
p.Asn496His(p.N496H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000319004 |
| Start |
747746:747746(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs370552236
|
| CDS Mutation |
c.297G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |