| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373588 |
| Start |
124503204:124503204(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.119C>T |
| AA Mutation |
p.Thr40Met(p.T40M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373588 |
| Start |
124500653:124500653(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.307C>T |
| AA Mutation |
p.Arg103Trp(p.R103W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000373588 |
| Start |
124491106:124491106(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1113C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |