7-17318249-T-G

Variant names:

• chr7-17318249-T-G
• rs1476080
• NM_001621.5:c.254-4252T>G

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001621.5(AHR):​c.254-4252T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.582 in 151,722 control chromosomes in the GnomAD database, including 26,373 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.58 (26373 hom., cov: 31)
• Consequence: AHR NM_001621.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0230

Genes affected

AHR (HGNC:348): (aryl hydrocarbon receptor) The protein encoded by this gene is a ligand-activated helix-loop-helix transcription factor involved in the regulation of biological responses to planar aromatic hydrocarbons. This receptor has been shown to regulate xenobiotic-metabolizing enzymes such as cytochrome P450. Before ligand binding, the encoded protein is sequestered in the cytoplasm; upon ligand binding, this protein moves to the nucleus and stimulates transcription of target genes. [provided by RefSeq, Sep 2015]

ENSG00000283321 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.626 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
AHR	NM_001621.5	c.254-4252T>G		intron_variant	Intron 2 of 10	ENST00000242057.9	NP_001612.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
AHR	ENST00000242057.9	c.254-4252T>G		intron_variant	Intron 2 of 10	1	NM_001621.5	ENSP00000242057.4
ENSG00000283321	ENST00000637807.1	c.224-4252T>G		intron_variant	Intron 2 of 11	5		ENSP00000490530.1
AHR	ENST00000463496.1	n.254-4252T>G		intron_variant	Intron 2 of 11	1		ENSP00000436466.1
AHR	ENST00000642825.1	c.209-4252T>G		intron_variant	Intron 6 of 14			ENSP00000495987.1

Frequencies

GnomAD3 genomes AF: 0.583 AC: 88316 AN: 151602 Hom.: 26367 Cov.: 31

Gnomad AFR AF: 0.555

Gnomad AMI AF: 0.686

Gnomad AMR AF: 0.424

Gnomad ASJ AF: 0.635

Gnomad EAS AF: 0.383

Gnomad SAS AF: 0.580

Gnomad FIN AF: 0.680

Gnomad MID AF: 0.570

Gnomad NFE AF: 0.631

Gnomad OTH AF: 0.601

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.582 AC: 88348 AN: 151722 Hom.: 26373 Cov.: 31 AF XY: 0.581 AC XY: 43062 AN XY: 74148

Gnomad4 AFR AF: 0.555

Gnomad4 AMR AF: 0.423

Gnomad4 ASJ AF: 0.635

Gnomad4 EAS AF: 0.382

Gnomad4 SAS AF: 0.578

Gnomad4 FIN AF: 0.680

Gnomad4 NFE AF: 0.631

Gnomad4 OTH AF: 0.600

Alfa AF: 0.609 Hom.: 35596

Bravo AF: 0.562

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	2.0
DANN	Benign	0.63

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs1476080; hg19: chr7-17357873;