| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000242786 |
| Start |
14404407:14404407(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1474G>A |
| AA Mutation |
p.Glu492Lys(p.E492K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000242786 |
| Start |
14391027:14391027(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.294G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000242786 |
| Start |
14407064:14407064(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs757577314
|
| CDS Mutation |
c.2211G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |