| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000253332 |
| Start |
151350882:151350882(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2491G>A |
| AA Mutation |
p.Ala831Thr(p.A831T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000253332 |
| Start |
151348818:151348818(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.427C>A |
| AA Mutation |
p.Pro143Thr(p.P143T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000253332 |
| Start |
151351592:151351592(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3201G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |