rs10503913

Variant names:

• chr8-32376597-G-A
• rs10503913
• ENST00000520407.5:c.746-219231G>A

Your query was ambiguous. Multiple possible variants found:

• chr8-32376597-G-A
• chr8-32376597-G-C
• chr8-32376597-G-T

Variant summary

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

The NM_001159999.3(NRG1):​c.38-219231G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.823 in 152,152 control chromosomes in the GnomAD database, including 51,627 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 0.82 (51627 hom., cov: 32)
• Consequence: NRG1 NM_001159999.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0790
• Publications: 5 publications found

Genes affected

NRG1 (HGNC:7997): (neuregulin 1) The protein encoded by this gene is a membrane glycoprotein that mediates cell-cell signaling and plays a critical role in the growth and development of multiple organ systems. An extraordinary variety of different isoforms are produced from this gene through alternative promoter usage and splicing. These isoforms are expressed in a tissue-specific manner and differ significantly in their structure, and are classified as types I, II, III, IV, V and VI. Dysregulation of this gene has been linked to diseases such as cancer, schizophrenia, and bipolar disorder (BPD). [provided by RefSeq, Apr 2016]

NRG1 Gene-Disease associations (from GenCC):

• schizophrenia 6

  Inheritance: AR Classification: LIMITED Submitted by: Ambry Genetics

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.831 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001159999.3. 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
	NRG1	NM_001159999.3		c.38-219231G>A		intron	N/A	NP_001153471.1	A0A494C1F5
	NRG1	NM_001159995.3		c.38-219231G>A		intron	N/A	NP_001153467.1	A0A494C1F8
	NRG1	NM_001160001.3		c.38-219231G>A		intron	N/A	NP_001153473.1	Q02297-11

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	NRG1	ENST00000520407.5	TSL:1	c.746-219231G>A		intron	N/A	ENSP00000434640.1	Q02297-9
	NRG1	ENST00000523534.5	TSL:5	c.305-219231G>A		intron	N/A	ENSP00000429067.1	H0YBA3
	NRG1	ENST00000650866.1		c.38-219231G>A		intron	N/A	ENSP00000499045.1	A0A494C1F5

Frequencies

GnomAD3 genomes AF: 0.823 AC: 125105 AN: 152034 Hom.: 51587 Cov.: 32

Gnomad AFR AF: 0.799

Gnomad AMI AF: 0.668

Gnomad AMR AF: 0.842

Gnomad ASJ AF: 0.933

Gnomad EAS AF: 0.837

Gnomad SAS AF: 0.802

Gnomad FIN AF: 0.773

Gnomad MID AF: 0.896

Gnomad NFE AF: 0.837

Gnomad OTH AF: 0.839

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

GnomAD4 genome AF: 0.823 AC: 125202 AN: 152152 Hom.: 51627 Cov.: 32 AF XY: 0.821 AC XY: 61044 AN XY: 74388

African (AFR) AF: 0.800 AC: 33189 AN: 41506

American (AMR) AF: 0.841 AC: 12857 AN: 15282

Ashkenazi Jewish (ASJ) AF: 0.933 AC: 3239 AN: 3470

East Asian (EAS) AF: 0.837 AC: 4327 AN: 5168

South Asian (SAS) AF: 0.804 AC: 3878 AN: 4826

European-Finnish (FIN) AF: 0.773 AC: 8179 AN: 10584

Middle Eastern (MID) AF: 0.901 AC: 265 AN: 294

European-Non Finnish (NFE) AF: 0.837 AC: 56891 AN: 67998

Other (OTH) AF: 0.837 AC: 1769 AN: 2114

Alfa AF: 0.834 Hom.: 146987

Bravo AF: 0.829

Asia WGS AF: 0.808 AC: 2811 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	2.2
DANN	Benign	0.24
PhyloP100		0.079
Mutation Taster		=100/0	polymorphism (auto)

Splicing

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

Other links and lift over

dbSNP: rs10503913; hg19: chr8-32234113; COSMIC: COSV73066203;