| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000233735 |
| Start |
79121628:79121628(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs777579151
|
| CDS Mutation |
c.131G>A |
| AA Mutation |
p.Arg44His(p.R44H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000233735 |
| Start |
79121632:79121632(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.135C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000233735 |
| Start |
79122879:79122879(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.360C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |