| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000253332 |
| Start |
151352403:151352403(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4012G>A |
| AA Mutation |
p.Val1338Ile(p.V1338I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000253332 |
| Start |
151305809:151305809(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.225C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
protein_altering_variant |
| Transcription ID |
ENST00000253332 |
| Start |
151352980:151352981(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4589_4590insGGA |
| AA Mutation |
p.Ile1530delinsMetAsp(p.I1530delinsMD) |
| Mutation Classification |
In_Frame_Ins |
| Feature Type |
Transcript |