| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000327968 |
| Start |
23001510:23001510(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1453A>G |
| AA Mutation |
p.Ser485Gly(p.S485G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000327968 |
| Start |
23000315:23000315(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs778444531
|
| CDS Mutation |
c.258C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000327968 |
| Start |
23001455:23001455(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1398C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |