| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000340736 |
| Start |
14160222:14160222(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1705G>A |
| AA Mutation |
p.Asp569Asn(p.D569N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000340736 |
| Start |
14177715:14177715(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.100C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000340736 |
| Start |
14163384:14163384(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.432G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |