| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262836 |
| Start |
111173071:111173071(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.865A>G |
| AA Mutation |
p.Ile289Val(p.I289V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262836 |
| Start |
111216517:111216517(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1549A>T |
| AA Mutation |
p.Met517Leu(p.M517L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262836 |
| Start |
111195892:111195892(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1206T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |