| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000374003 |
| Start |
27623096:27623096(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.275C>A |
| AA Mutation |
p.Thr92Asn(p.T92N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000374003 |
| Start |
27613249:27613249(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1351C>A |
| AA Mutation |
p.Leu451Ile(p.L451I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000374003 |
| Start |
27614865:27614865(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1080G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |