| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371205 |
| Start |
95842445:95842445(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.364C>A |
| AA Mutation |
p.Gln122Lys(p.Q122K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000371205 |
| Start |
95866263:95866263(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1413T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000371205 |
| Start |
95866353:95866353(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs750517800
|
| CDS Mutation |
c.1503G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |