| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000318445 |
| Start |
92147137:92147137(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1666C>T |
| AA Mutation |
p.Pro556Ser(p.P556S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000318445 |
| Start |
91916448:91916448(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs768503651
|
| CDS Mutation |
c.636G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000318445 |
| Start |
92104346:92104346(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs552651566
|
| CDS Mutation |
c.813C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |