| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000442250 |
| Start |
172474195:172474195(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1033A>G |
| AA Mutation |
p.Ile345Val(p.I345V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000442250 |
| Start |
172491066:172491066(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2839C>G |
| AA Mutation |
p.Gln947Glu(p.Q947E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000442250 |
| Start |
172479677:172479677(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1542A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |