| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361034 |
| Start |
46664030:46664030(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs202227527
|
| CDS Mutation |
c.630C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
splice_acceptor_variant |
| Transcription ID |
ENST00000361034 |
| Start |
46677145:46677145(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1633-2A>T |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000361034 |
| Start |
46637961:46637961(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.283+1G>C |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |