rs638169

Variant names:

• chr15-33976135-G-A
• rs638169
• NM_012125.4:c.-408+6985G>A

Your query was ambiguous. Multiple possible variants found:

• chr15-33976135-G-A
• chr15-33976135-G-C
• chr15-33976135-G-T

Variant summary

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

The NM_012125.4(CHRM5):​c.-408+6985G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.775 in 152,066 control chromosomes in the GnomAD database, including 52,933 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 0.78 (52933 hom., cov: 31)
• Consequence: CHRM5 NM_012125.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.668
• Publications: 4 publications found

Genes affected

CHRM5 (HGNC:1954): (cholinergic receptor muscarinic 5) The muscarinic cholinergic receptors belong to a larger family of G protein-coupled receptors. The functional diversity of these receptors is defined by the binding of acetylcholine and includes cellular responses such as adenylate cyclase inhibition, phosphoinositide degeneration, and potassium channel mediation. Muscarinic receptors influence many effects of acetylcholine in the central and peripheral nervous system. The clinical implications of this receptor are unknown; however, stimulation of this receptor is known to increase cyclic AMP levels. [provided by RefSeq, Jul 2008]

AVEN (HGNC:13509): (apoptosis and caspase activation inhibitor) Involved in negative regulation of apoptotic process. Located in membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.97 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_012125.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CHRM5	NM_012125.4	MANE Select	c.-408+6985G>A		intron	N/A	NP_036257.1
	AVEN	NM_020371.3	MANE Select	c.445+26897C>T		intron	N/A	NP_065104.1
	CHRM5	NM_001320917.2		c.-76+6985G>A		intron	N/A	NP_001307846.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CHRM5	ENST00000383263.7	TSL:2 MANE Select	c.-408+6985G>A		intron	N/A	ENSP00000372750.5
	AVEN	ENST00000306730.8	TSL:1 MANE Select	c.445+26897C>T		intron	N/A	ENSP00000306822.3
	CHRM5	ENST00000560035.1	TSL:4	c.-76+6985G>A		intron	N/A	ENSP00000452742.1

Frequencies

GnomAD3 genomes AF: 0.776 AC: 117872 AN: 151948 Hom.: 52931 Cov.: 31

Gnomad AFR AF: 0.281

Gnomad AMI AF: 0.987

Gnomad AMR AF: 0.894

Gnomad ASJ AF: 0.991

Gnomad EAS AF: 0.918

Gnomad SAS AF: 0.946

Gnomad FIN AF: 0.994

Gnomad MID AF: 0.911

Gnomad NFE AF: 0.976

Gnomad OTH AF: 0.834

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

GnomAD4 genome AF: 0.775 AC: 117892 AN: 152066 Hom.: 52933 Cov.: 31 AF XY: 0.783 AC XY: 58218 AN XY: 74360

African (AFR) AF: 0.281 AC: 11622 AN: 41374

American (AMR) AF: 0.895 AC: 13670 AN: 15280

Ashkenazi Jewish (ASJ) AF: 0.991 AC: 3441 AN: 3472

East Asian (EAS) AF: 0.918 AC: 4754 AN: 5176

South Asian (SAS) AF: 0.946 AC: 4560 AN: 4820

European-Finnish (FIN) AF: 0.994 AC: 10547 AN: 10616

Middle Eastern (MID) AF: 0.912 AC: 268 AN: 294

European-Non Finnish (NFE) AF: 0.976 AC: 66365 AN: 68008

Other (OTH) AF: 0.835 AC: 1765 AN: 2114

Alfa AF: 0.869 Hom.: 10598

Bravo AF: 0.745

Asia WGS AF: 0.881 AC: 3061 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	3.3
DANN	Benign	0.43
PhyloP100		0.67
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: rs638169; hg19: chr15-34268336;