| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000309951 |
| Start |
32418352:32418352(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.499A>G |
| AA Mutation |
p.Met167Val(p.M167V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000309951 |
| Start |
32450105:32450105(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2664C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000309951 |
| Start |
32430522:32430522(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1674A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |