| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000432992 |
| Start |
9969723:9969723(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.425C>A |
| AA Mutation |
p.Pro142Gln(p.P142Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000432992 |
| Start |
9943183:9943183(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.669G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000432992 |
| Start |
9946892:9946892(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.615+2T>C |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |