| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265085 |
| Start |
173910526:173910526(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1129C>T |
| AA Mutation |
p.Arg377Cys(p.R377C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265085 |
| Start |
173951897:173951897(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1739A>C |
| AA Mutation |
p.Lys580Thr(p.K580T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265085 |
| Start |
173889985:173889985(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.252A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |