| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000308873 |
| Start |
24902631:24902631(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.739C>A |
| AA Mutation |
p.Gln247Lys(p.Q247K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000308873 |
| Start |
24902620:24902620(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.750C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000308873 |
| Start |
24902632:24902632(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.738C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |