| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262551 |
| Start |
92385639:92385639(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.878C>G |
| AA Mutation |
p.Pro293Arg(p.P293R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262551 |
| Start |
92389946:92389946(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs746882470
|
| CDS Mutation |
c.538C>G |
| AA Mutation |
p.Leu180Val(p.L180V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262551 |
| Start |
92393099:92393099(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.414T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |