| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000375559 |
| Start |
113149256:113149256(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1206G>A |
| AA Mutation |
p.Met402Ile(p.M402I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000375559 |
| Start |
113140973:113140973(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.425A>T |
| AA Mutation |
p.Glu142Val(p.E142V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000375559 |
| Start |
113148944:113148944(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs778741024
|
| CDS Mutation |
c.894C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |