| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000252677 |
| Start |
50910812:50910812(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.29T>G |
| AA Mutation |
p.Leu10Arg(p.L10R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000252677 |
| Start |
50915924:50915924(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.496T>A |
| AA Mutation |
p.Ser166Thr(p.S166T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000252677 |
| Start |
50916241:50916241(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.813T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |