| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000336735 |
| Start |
81489282:81489282(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1365G>T |
| AA Mutation |
p.Met455Ile(p.M455I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000336735 |
| Start |
81477154:81477154(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2203A>G |
| AA Mutation |
p.Met735Val(p.M735V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000336735 |
| Start |
81498459:81498459(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.927G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |