Gene >> NCAPG
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000251496 |
| Start |
17843355:17843355(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs757772284
|
| CDS Mutation |
c.2978G>A |
| AA Mutation |
p.Arg993Gln(p.R993Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000251496 |
| Start |
17837646:17837646(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2311G>C |
| AA Mutation |
p.Glu771Gln(p.E771Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |