| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000399916 |
| Start |
24964540:24964540(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.32C>T |
| AA Mutation |
p.Pro11Leu(p.P11L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000308873 |
| Start |
24902521:24902521(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs779004787
|
| CDS Mutation |
c.849G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000308873 |
| Start |
24902587:24902587(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.783C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |