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chr17_80036614_C_A

chr17:80036614 · GRCh38CArs2037059075gnomAD AF 12.6%receptor_confirmed

Regulatory target CCDC40 is taken from a GTEx liver eQTL, not from distance. For a non-coding regulatory variant the nearest gene by distance is frequently not the regulated gene.

Receptor variant-effect scores

PXR
-0.011Neutral
FXR
0.076Neutral
AhR
0.404GoF
-1 LoF0+1 GoF

Strongest effect: AhR GoF at p99-scaled 0.404. 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

ClinVar
Benign · not provided
GTEx liver eQTL
CCDC40, slope 0.89, p 2.1e-18
phyloP conservation
0.96
gnomAD
AF 12.6%
dbSNP
rs2037059075
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-0.0110.0760.40412.6%
CG-0.161-0.128-0.618not observed
CT0.1300.1310.494not observed

Every possible base substitution at chr17:80036614, 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: PXRAhR

Multi receptor overlap: PXR,AhR