| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000205557 |
| Start |
16150762:16150762(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4219A>G |
| AA Mutation |
p.Lys1407Glu(p.K1407E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000205557 |
| Start |
16150594:16150594(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.4387G>T |
| AA Mutation |
p.Val1463Leu(p.V1463L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000205557 |
| Start |
16161498:16161498(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3573G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |