| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368006 |
| Start |
161123198:161123198(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.457T>C |
| AA Mutation |
p.Cys153Arg(p.C153R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368006 |
| Start |
161124335:161124335(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs764036709
|
| CDS Mutation |
c.128G>A |
| AA Mutation |
p.Arg43His(p.R43H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000368006 |
| Start |
161122297:161122297(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.807A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |