| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000340736 |
| Start |
14163139:14163139(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.677A>C |
| AA Mutation |
p.Asn226Thr(p.N226T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000340736 |
| Start |
14155374:14155374(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs770806298
|
| CDS Mutation |
c.3294C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000340736 |
| Start |
14157068:14157068(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2838G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |