| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000342833 |
| Start |
68303012:68303012(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.61G>A |
| AA Mutation |
p.Asp21Asn(p.D21N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000342833 |
| Start |
68304075:68304075(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1124C>T |
| AA Mutation |
p.Pro375Leu(p.P375L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000342833 |
| Start |
68303812:68303812(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.861C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |