| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000283268 |
| Start |
62370278:62370278(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1185C>G |
| AA Mutation |
p.Asn395Lys(p.N395K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000283268 |
| Start |
62372473:62372473(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.396C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000283268 |
| Start |
62372557:62372557(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.312C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |