| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000441310 |
| Start |
189795857:189795857(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.221A>G |
| AA Mutation |
p.Tyr74Cys(p.Y74C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000441310 |
| Start |
189867919:189867919(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2463A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000441310 |
| Start |
189795906:189795906(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs149723996
|
| CDS Mutation |
c.270C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |