| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000324138 |
| Start |
14845159:14845159(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1624C>G |
| AA Mutation |
p.Pro542Ala(p.P542A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000324138 |
| Start |
14843885:14843885(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2262C>G |
| AA Mutation |
p.Phe754Leu(p.F754L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000324138 |
| Start |
14845280:14845280(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1503G>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |