| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261937 |
| Start |
180611335:180611335(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs369284915
|
| CDS Mutation |
c.3682G>A |
| AA Mutation |
p.Ala1228Thr(p.A1228T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261937 |
| Start |
180616381:180616381(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs760077499
|
| CDS Mutation |
c.3205G>A |
| AA Mutation |
p.Val1069Ile(p.V1069I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000261937 |
| Start |
180631729:180631729(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.108G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |