| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000285879 |
| Start |
141907943:141907943(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2539C>A |
| AA Mutation |
p.Pro847Thr(p.P847T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000285879 |
| Start |
141905679:141905679(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.275C>T |
| AA Mutation |
p.Thr92Ile(p.T92I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000285879 |
| Start |
141906816:141906816(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1412A>T |
| AA Mutation |
p.Glu471Val(p.E471V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |