| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000281708 |
| Start |
152332655:152332655(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs760675122
|
| CDS Mutation |
c.926G>A |
| AA Mutation |
p.Arg309His(p.R309H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000281708 |
| Start |
152332689:152332689(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.892C>A |
| AA Mutation |
p.Pro298Thr(p.P298T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000281708 |
| Start |
152324302:152324302(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1737G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |