| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000255499 |
| Start |
106772925:106772925(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.497T>G |
| AA Mutation |
p.Ile166Ser(p.I166S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000255499 |
| Start |
106773081:106773081(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.653T>G |
| AA Mutation |
p.Ile218Ser(p.I218S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000255499 |
| Start |
106726997:106726997(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.84C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |