| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000223095 |
| Start |
101133875:101133875(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.881G>A |
| AA Mutation |
p.Arg294His(p.R294H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000223095 |
| Start |
101130506:101130506(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs6091
|
| CDS Mutation |
c.357G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000223095 |
| Start |
101135770:101135770(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs538551265
|
| CDS Mutation |
c.1056C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |