| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000379561 |
| Start |
40666148:40666148(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.65C>G |
| AA Mutation |
p.Ser22Trp(p.S22W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000379561 |
| Start |
40665655:40665655(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs754690688
|
| CDS Mutation |
c.558C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000379561 |
| Start |
40560666:40560666(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.825A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |