| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000338316 |
| Start |
7712890:7712890(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs767145470
|
| CDS Mutation |
c.1613G>A |
| AA Mutation |
p.Arg538His(p.R538H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000338316 |
| Start |
7727187:7727187(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs778398128
|
| CDS Mutation |
c.1797G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000338316 |
| Start |
7717163:7717163(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1629G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |