rs11761434

Variant names:

• chr7-129650719-G-A
• rs11761434
• NM_005011.5:c.-6-6627G>A

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_005011.5(NRF1):​c.-6-6627G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.302 in 151,656 control chromosomes in the GnomAD database, including 8,509 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 0.30 (8509 hom., cov: 30)
• Consequence: NRF1 NM_005011.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0590
• Publications: 3 publications found

Genes affected

NRF1 (HGNC:7996): (nuclear respiratory factor 1) This gene encodes a protein that homodimerizes and functions as a transcription factor which activates the expression of some key metabolic genes regulating cellular growth and nuclear genes required for respiration, heme biosynthesis, and mitochondrial DNA transcription and replication. The protein has also been associated with the regulation of neurite outgrowth. Alternative splicing results in multiple transcript variants. Confusion has occurred in bibliographic databases due to the shared symbol of NRF1 for this gene and for "nuclear factor (erythroid-derived 2)-like 1" which has an official symbol of NFE2L1. [provided by RefSeq, May 2014]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.421 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
NRF1	NM_005011.5	c.-6-6627G>A		intron_variant	Intron 1 of 10	ENST00000393232.6	NP_005002.3
NRF1	NM_001293163.2	c.-9-6624G>A		intron_variant	Intron 1 of 11		NP_001280092.1
NRF1	NM_001040110.2	c.-9-6624G>A		intron_variant	Intron 1 of 10		NP_001035199.1
NRF1	NM_001293164.2	c.-377-6624G>A		intron_variant	Intron 1 of 9		NP_001280093.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
NRF1	ENST00000393232.6	c.-6-6627G>A		intron_variant	Intron 1 of 10	1	NM_005011.5	ENSP00000376924.1

Frequencies

GnomAD3 genomes AF: 0.302 AC: 45741 AN: 151538 Hom.: 8509 Cov.: 30

Gnomad AFR AF: 0.101

Gnomad AMI AF: 0.495

Gnomad AMR AF: 0.257

Gnomad ASJ AF: 0.491

Gnomad EAS AF: 0.0949

Gnomad SAS AF: 0.287

Gnomad FIN AF: 0.379

Gnomad MID AF: 0.350

Gnomad NFE AF: 0.425

Gnomad OTH AF: 0.317

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

GnomAD4 genome AF: 0.302 AC: 45736 AN: 151656 Hom.: 8509 Cov.: 30 AF XY: 0.297 AC XY: 22038 AN XY: 74104

African (AFR) AF: 0.101 AC: 4190 AN: 41310

American (AMR) AF: 0.257 AC: 3912 AN: 15250

Ashkenazi Jewish (ASJ) AF: 0.491 AC: 1703 AN: 3468

East Asian (EAS) AF: 0.0951 AC: 490 AN: 5152

South Asian (SAS) AF: 0.287 AC: 1375 AN: 4798

European-Finnish (FIN) AF: 0.379 AC: 3978 AN: 10488

Middle Eastern (MID) AF: 0.349 AC: 102 AN: 292

European-Non Finnish (NFE) AF: 0.425 AC: 28880 AN: 67886

Other (OTH) AF: 0.312 AC: 656 AN: 2102

Alfa AF: 0.355 Hom.: 1381

Bravo AF: 0.284

Asia WGS AF: 0.161 AC: 560 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
CADD	Benign	1.5
DANN	Benign	0.77
PhyloP100		0.059
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs11761434; hg19: chr7-129290559;