| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000239007 |
| Start |
110280068:110280068(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs140539151
|
| CDS Mutation |
c.506G>A |
| AA Mutation |
p.Arg169His(p.R169H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000332674 |
| Start |
110207916:110207916(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.108G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000239007 |
| Start |
110228229:110228229(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.114G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |