| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000257189 |
| Start |
31459048:31459048(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.388C>A |
| AA Mutation |
p.Leu130Ile(p.L130I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000257189 |
| Start |
31472288:31472288(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1902C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000257189 |
| Start |
31459087:31459087(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.427C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |