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chr17_63947092_G_T

chr17:63947092 · GRCh38GTrs1597970512receptor_confirmed

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

Receptor variant-effect scores

PXR
-0.013Neutral
FXR
0.003Neutral
AhR
-0.073Neutral
-1 (LoF)0+1 (GoF)

Strongest effect: AhR Neutral at normalized -0.073. Impact is low, near neutral.

ft_head_delta_norm = center bin sum of ALT minus REF on the receptor CHIP_TF head, normalized to the peak population 99th percentile and clipped to [−1, 1]. AhR is reported as exploratory, single replicate.

Cross-annotations

ClinVar
Likely benign · Hyperkalemic periodic paralysis · record
phyloP conservation
0.52
dbSNP
rs1597970512
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
GA-0.0100.008-0.062not observed
GC-0.011-0.006-0.129not observed
GT-0.0130.003-0.073not observed

Every possible base substitution at chr17:63947092, each scored independently. 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: PXR

Multi receptor overlap: PXR

Binding motif

Logo for the strongest scoring receptor, AhR. The highlighted column marks the approximate affected base within the response element. External browser: UCSC Genome Browser.