| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260227 |
| Start |
102527860:102527860(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs145006821
|
| CDS Mutation |
c.232G>A |
| AA Mutation |
p.Val78Ile(p.V78I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260227 |
| Start |
102524959:102524959(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs765986644
|
| CDS Mutation |
c.590G>A |
| AA Mutation |
p.Arg197His(p.R197H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000260227 |
| Start |
102525024:102525024(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs752373573
|
| CDS Mutation |
c.525G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |