Gene >> KL
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380099 |
| Start |
33061136:33061136(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs141695559
|
| CDS Mutation |
c.2057C>T |
| AA Mutation |
p.Thr686Met(p.T686M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000380099 |
| Start |
33061704:33061704(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs756905480
|
| CDS Mutation |
c.2625C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |