| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260810 |
| Start |
133656719:133656719(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.502C>A |
| AA Mutation |
p.Leu168Ile(p.L168I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260810 |
| Start |
133608893:133608893(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4243C>T |
| AA Mutation |
p.Leu1415Phe(p.L1415F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000260810 |
| Start |
133618373:133618373(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3432T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |