| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000527614 |
| Start |
111753498:111753498(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1109A>G |
| AA Mutation |
p.Lys370Arg(p.K370R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000527614 |
| Start |
111743466:111743466(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1464G>T |
| AA Mutation |
p.Glu488Asp(p.E488D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000527614 |
| Start |
111752270:111752270(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1227C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |