| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000249363 |
| Start |
128030178:128030178(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.463C>T |
| AA Mutation |
p.Arg155Cys(p.R155C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000249363 |
| Start |
128030177:128030177(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.464G>A |
| AA Mutation |
p.Arg155His(p.R155H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000249363 |
| Start |
128029851:128029851(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.790G>A |
| AA Mutation |
p.Gly264Arg(p.G264R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |