rs1909884

Variant names:

• chr15-32147097-G-A
• rs1909884
• NM_000746.6:c.351-6810G>A

Your query was ambiguous. Multiple possible variants found:

• chr15-32147097-G-A
• chr15-32147097-G-C
• chr15-32147097-G-T

Variant summary

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

The NM_000746.6(CHRNA7):​c.351-6810G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.408 in 152,104 control chromosomes in the GnomAD database, including 13,000 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 (13000 hom., cov: 33)
• Consequence: CHRNA7 NM_000746.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.543
• Publications: 17 publications found

Genes affected

CHRNA7 (HGNC:1960): (cholinergic receptor nicotinic alpha 7 subunit) The nicotinic acetylcholine receptors (nAChRs) are members of a superfamily of ligand-gated ion channels that mediate fast signal transmission at synapses. The nAChRs are thought to be hetero-pentamers composed of homologous subunits. The proposed structure for each subunit is a conserved N-terminal extracellular domain followed by three conserved transmembrane domains, a variable cytoplasmic loop, a fourth conserved transmembrane domain, and a short C-terminal extracellular region. The protein encoded by this gene forms a homo-oligomeric channel, displays marked permeability to calcium ions and is a major component of brain nicotinic receptors that are blocked by, and highly sensitive to, alpha-bungarotoxin. Once this receptor binds acetylcholine, it undergoes an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. This gene is located in a region identified as a major susceptibility locus for juvenile myoclonic epilepsy and a chromosomal location involved in the genetic transmission of schizophrenia. An evolutionarily recent partial duplication event in this region results in a hybrid containing sequence from this gene and a novel FAM7A gene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]

CHRNA7 Gene-Disease associations (from GenCC):

• complex neurodevelopmental disorder

  Inheritance: AD Classification: LIMITED Submitted by: Ambry Genetics
• epilepsy

  Inheritance: Unknown Classification: NO_KNOWN Submitted by: ClinGen

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.97).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.509 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_000746.6. 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
	CHRNA7	NM_000746.6	MANE Select	c.351-6810G>A		intron	N/A	NP_000737.1	P36544-1
	CHRNA7	NM_001190455.3		c.438-6810G>A		intron	N/A	NP_001177384.1	P36544-2
	CHRNA7	NR_046324.1		n.353-10511G>A		intron	N/A

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CHRNA7	ENST00000306901.9	TSL:1 MANE Select	c.351-6810G>A		intron	N/A	ENSP00000303727.2	P36544-1
	CHRNA7	ENST00000454250.7	TSL:2	c.438-6810G>A		intron	N/A	ENSP00000407546.3	P36544-2
	CHRNA7	ENST00000675428.1		c.438-6810G>A		intron	N/A	ENSP00000502560.1	P36544-2

Frequencies

GnomAD3 genomes AF: 0.408 AC: 62025 AN: 151986 Hom.: 12986 Cov.: 33

Gnomad AFR AF: 0.516

Gnomad AMI AF: 0.332

Gnomad AMR AF: 0.412

Gnomad ASJ AF: 0.363

Gnomad EAS AF: 0.249

Gnomad SAS AF: 0.395

Gnomad FIN AF: 0.343

Gnomad MID AF: 0.408

Gnomad NFE AF: 0.369

Gnomad OTH AF: 0.393

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

GnomAD4 genome AF: 0.408 AC: 62069 AN: 152104 Hom.: 13000 Cov.: 33 AF XY: 0.407 AC XY: 30235 AN XY: 74352

African (AFR) AF: 0.515 AC: 21365 AN: 41470

American (AMR) AF: 0.412 AC: 6297 AN: 15280

Ashkenazi Jewish (ASJ) AF: 0.363 AC: 1261 AN: 3470

East Asian (EAS) AF: 0.249 AC: 1290 AN: 5182

South Asian (SAS) AF: 0.396 AC: 1907 AN: 4816

European-Finnish (FIN) AF: 0.343 AC: 3632 AN: 10586

Middle Eastern (MID) AF: 0.401 AC: 118 AN: 294

European-Non Finnish (NFE) AF: 0.369 AC: 25071 AN: 67982

Other (OTH) AF: 0.391 AC: 825 AN: 2112

Alfa AF: 0.376 Hom.: 30219

Bravo AF: 0.416

Asia WGS AF: 0.376 AC: 1305 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.97
CADD	Benign	5.5
DANN	Benign	0.63
PhyloP100		0.54
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: rs1909884; hg19: chr15-32439298;