| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261921 |
| Start |
73949540:73949540(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1684C>T |
| AA Mutation |
p.Arg562Cys(p.R562C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261921 |
| Start |
73947873:73947873(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs772638560
|
| CDS Mutation |
c.1573G>A |
| AA Mutation |
p.Asp525Asn(p.D525N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000261921 |
| Start |
73947100:73947100(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs748019800
|
| CDS Mutation |
c.1383C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |