Home / Variant

chr14_69398319_C_T

chr14:69398319 · GRCh38CTrs1335278221gnomAD AF 0.0066%receptor_confirmed

For a non-coding regulatory variant the nearest gene by distance is frequently not the regulated gene.

Receptor variant-effect scores

PXR
-0.298LoF
FXR
0.131GoF
AhR
-0.164LoF
-1 LoF0+1 GoF

Strongest effect: PXR LoF at p99-scaled -0.298. Impact is moderate on the receptor-specific p99 scale.

The p99-scaled score divides the raw delta by the receptor-specific 99th percentile of |delta| in the reference peak population, then clips to −1 to 1. It is a comparable effect scale, not a percentile rank. AhR is exploratory, from a single replicate.

Cross-annotations

phyloP conservation
1.90
gnomAD
AF 0.0066%
dbSNP
rs1335278221
Region tier
receptor_confirmed

Mirrored from ClinVar, GTEx, GWAS Catalog, JASPAR/FIMO, gnomAD and phyloP. See Databases.

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
CA-0.3310.151-0.246not observed
CG-0.2950.159-0.117not observed
CT-0.2980.131-0.1640.0066%

Every possible base substitution at chr14:69398319, each scored independently and shown as p99-scaled scores. The gnomAD column shows which substitution is actually seen in the population versus in silico only. Region confidence is the same for every substitution at this position, so it is shown once in the section below.

Region confidence

In receptor peaks: AhR