| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000621411 |
| Start |
26031981:26031981(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.80G>A |
| AA Mutation |
p.Arg27His(p.R27H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000621411 |
| Start |
26031778:26031778(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.283G>A |
| AA Mutation |
p.Glu95Lys(p.E95K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000621411 |
| Start |
26031998:26031998(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.63G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |