| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000369915 |
| Start |
154327667:154327667(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1478C>T |
| AA Mutation |
p.Ala493Val(p.A493V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000369915 |
| Start |
154329656:154329656(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1759A>T |
| AA Mutation |
p.Ile587Leu(p.I587L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000369915 |
| Start |
154327954:154327954(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1614G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |