| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000257552 |
| Start |
120357863:120357863(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.487G>A |
| AA Mutation |
p.Val163Met(p.V163M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000257552 |
| Start |
120368073:120368073(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.202T>G |
| AA Mutation |
p.Phe68Val(p.F68V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000257552 |
| Start |
120347474:120347474(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs561139090
|
| CDS Mutation |
c.831G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |