NM_005235.3:c.82+15273G>A

Variant names:

• chr2-212523176-C-T
• rs7564590
• NM_005235.3:c.82+15273G>A

Variant summary

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

The NM_005235.3(ERBB4):​c.82+15273G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.411 in 151,634 control chromosomes in the GnomAD database, including 14,790 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 0.41 (14790 hom., cov: 32)
• Consequence: ERBB4 NM_005235.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.154
• Publications: 13 publications found

Genes affected

ERBB4 (HGNC:3432): (erb-b2 receptor tyrosine kinase 4) This gene is a member of the Tyr protein kinase family and the epidermal growth factor receptor subfamily. It encodes a single-pass type I membrane protein with multiple cysteine rich domains, a transmembrane domain, a tyrosine kinase domain, a phosphotidylinositol-3 kinase binding site and a PDZ domain binding motif. The protein binds to and is activated by neuregulins and other factors and induces a variety of cellular responses including mitogenesis and differentiation. Multiple proteolytic events allow for the release of a cytoplasmic fragment and an extracellular fragment. Mutations in this gene have been associated with cancer. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008]

ERBB4 Gene-Disease associations (from GenCC):

• amyotrophic lateral sclerosis type 19

  Inheritance: AD Classification: STRONG, MODERATE, LIMITED Submitted by: ClinGen, Ambry Genetics, Labcorp Genetics (formerly Invitae), Genomics England PanelApp
• amyotrophic lateral sclerosis

  Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.95).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.66 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_005235.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ERBB4	NM_005235.3	MANE Select	c.82+15273G>A		intron	N/A	NP_005226.1
	ERBB4	NM_001439005.1		c.82+15273G>A		intron	N/A	NP_001425934.1
	ERBB4	NM_001042599.2		c.82+15273G>A		intron	N/A	NP_001036064.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ERBB4	ENST00000342788.9	TSL:1 MANE Select	c.82+15273G>A		intron	N/A	ENSP00000342235.4
	ERBB4	ENST00000436443.5	TSL:1	c.82+15273G>A		intron	N/A	ENSP00000403204.1
	ERBB4	ENST00000484594.5	TSL:1	n.134+15273G>A		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.410 AC: 62151 AN: 151516 Hom.: 14739 Cov.: 32

Gnomad AFR AF: 0.666

Gnomad AMI AF: 0.280

Gnomad AMR AF: 0.326

Gnomad ASJ AF: 0.275

Gnomad EAS AF: 0.107

Gnomad SAS AF: 0.341

Gnomad FIN AF: 0.340

Gnomad MID AF: 0.272

Gnomad NFE AF: 0.323

Gnomad OTH AF: 0.365

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

GnomAD4 genome AF: 0.411 AC: 62273 AN: 151634 Hom.: 14790 Cov.: 32 AF XY: 0.407 AC XY: 30152 AN XY: 74108

African (AFR) AF: 0.667 AC: 27598 AN: 41382

American (AMR) AF: 0.326 AC: 4951 AN: 15196

Ashkenazi Jewish (ASJ) AF: 0.275 AC: 952 AN: 3462

East Asian (EAS) AF: 0.107 AC: 554 AN: 5160

South Asian (SAS) AF: 0.343 AC: 1647 AN: 4802

European-Finnish (FIN) AF: 0.340 AC: 3575 AN: 10514

Middle Eastern (MID) AF: 0.286 AC: 84 AN: 294

European-Non Finnish (NFE) AF: 0.323 AC: 21895 AN: 67802

Other (OTH) AF: 0.361 AC: 762 AN: 2110

Alfa AF: 0.388 Hom.: 2411

Bravo AF: 0.421

Asia WGS AF: 0.256 AC: 890 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.95
CADD	Benign	1.4
DANN	Benign	0.25
PhyloP100		-0.15
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: rs7564590; hg19: chr2-213387900;