| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000536262 |
| Start |
101166657:101166657(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs766865298
|
| CDS Mutation |
c.1363T>C |
| AA Mutation |
p.Trp455Arg(p.W455R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000536262 |
| Start |
101204510:101204510(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.407T>C |
| AA Mutation |
p.Ile136Thr(p.I136T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000536262 |
| Start |
101209836:101209836(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.13C>T |
| AA Mutation |
p.Arg5Trp(p.R5W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |