| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265512 |
| Start |
99126610:99126610(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1102A>G |
| AA Mutation |
p.Met368Val(p.M368V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265512 |
| Start |
99136504:99136504(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.544T>G |
| AA Mutation |
p.Phe182Val(p.F182V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265512 |
| Start |
99131543:99131543(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.804G>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |