| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000242783 |
| Start |
14467949:14467949(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1958C>T |
| AA Mutation |
p.Ala653Val(p.A653V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000242783 |
| Start |
14458047:14458047(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1182G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000242783 |
| Start |
14470848:14470848(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2622C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |