| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000407528 |
| Start |
85886228:85886228(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.403C>A |
| AA Mutation |
p.Pro135Thr(p.P135T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000407528 |
| Start |
85912377:85912377(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.507A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
splice_acceptor_variant |
| Transcription ID |
ENST00000407528 |
| Start |
86065603:86065603(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1064-2A>G |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |