| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000305579 |
| Start |
159990288:159990288(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.240G>T |
| AA Mutation |
p.Arg80Ser(p.R80S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000305579 |
| Start |
159993473:159993473(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.401G>C |
| AA Mutation |
p.Arg134Thr(p.R134T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000305579 |
| Start |
159993100:159993100(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.353C>T |
| AA Mutation |
p.Ala118Val(p.A118V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |