| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000404115 |
| Start |
120535882:120535882(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2162T>G |
| AA Mutation |
p.Leu721Arg(p.L721R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000404115 |
| Start |
120538171:120538171(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1945T>C |
| AA Mutation |
p.Phe649Leu(p.F649L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000404115 |
| Start |
120543768:120543768(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1269A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |