| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262367 |
| Start |
3757334:3757334(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3652C>A |
| AA Mutation |
p.Leu1218Met(p.L1218M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262367 |
| Start |
3773808:3773808(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs748195458
|
| CDS Mutation |
c.2406C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262367 |
| Start |
3728861:3728861(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs780383901
|
| CDS Mutation |
c.6186C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |