| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000297532 |
| Start |
151078967:151078967(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs761778464
|
| CDS Mutation |
c.560G>A |
| AA Mutation |
p.Arg187His(p.R187H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000297532 |
| Start |
151078846:151078846(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.681G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000297532 |
| Start |
151079828:151079828(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.177G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |