| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000245323 |
| Start |
106495768:106495768(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.479T>A |
| AA Mutation |
p.Ile160Asn(p.I160N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000245323 |
| Start |
106494947:106494947(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.547C>T |
| AA Mutation |
p.Pro183Ser(p.P183S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000245323 |
| Start |
106493415:106493415(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs768069785
|
| CDS Mutation |
c.627C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |