rs7578650

Variant names:

• chr2-124355398-A-G
• rs7578650
• NM_001367498.1:c.382-62045A>G

Your query was ambiguous. Multiple possible variants found:

• chr2-124355398-A-G
• chr2-124355398-A-T

Variant summary

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

The NM_001367498.1(CNTNAP5):​c.382-62045A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.544 in 151,926 control chromosomes in the GnomAD database, including 23,091 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 0.54 (23091 hom., cov: 31)
• Consequence: CNTNAP5 NM_001367498.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.44
• Publications: 5 publications found

Genes affected

CNTNAP5 (HGNC:18748): (contactin associated protein family member 5) This gene product belongs to the neurexin family, members of which function in the vertebrate nervous system as cell adhesion molecules and receptors. This protein, like other neurexin proteins, contains epidermal growth factor repeats and laminin G domains. In addition, it includes an F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, and thrombospondin N-terminal-like domains. [provided by RefSeq, Jul 2008]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.659 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CNTNAP5	NM_001367498.1	c.382-62045A>G		intron_variant	Intron 3 of 23	ENST00000682447.1	NP_001354427.1
CNTNAP5	NM_130773.4	c.382-62045A>G		intron_variant	Intron 3 of 23		NP_570129.1
CNTNAP5	XM_017003316.2	c.382-62045A>G		intron_variant	Intron 3 of 22		XP_016858805.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CNTNAP5	ENST00000682447.1	c.382-62045A>G		intron_variant	Intron 3 of 23		NM_001367498.1	ENSP00000508115.1
CNTNAP5	ENST00000431078.1	c.382-62045A>G		intron_variant	Intron 3 of 23	1		ENSP00000399013.1

Frequencies

GnomAD3 genomes AF: 0.544 AC: 82592 AN: 151808 Hom.: 23045 Cov.: 31

Gnomad AFR AF: 0.665

Gnomad AMI AF: 0.600

Gnomad AMR AF: 0.435

Gnomad ASJ AF: 0.542

Gnomad EAS AF: 0.428

Gnomad SAS AF: 0.414

Gnomad FIN AF: 0.553

Gnomad MID AF: 0.525

Gnomad NFE AF: 0.512

Gnomad OTH AF: 0.514

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

GnomAD4 genome AF: 0.544 AC: 82685 AN: 151926 Hom.: 23091 Cov.: 31 AF XY: 0.540 AC XY: 40094 AN XY: 74254

African (AFR) AF: 0.665 AC: 27558 AN: 41418

American (AMR) AF: 0.434 AC: 6627 AN: 15252

Ashkenazi Jewish (ASJ) AF: 0.542 AC: 1880 AN: 3470

East Asian (EAS) AF: 0.429 AC: 2212 AN: 5160

South Asian (SAS) AF: 0.416 AC: 2006 AN: 4826

European-Finnish (FIN) AF: 0.553 AC: 5831 AN: 10544

Middle Eastern (MID) AF: 0.527 AC: 155 AN: 294

European-Non Finnish (NFE) AF: 0.512 AC: 34791 AN: 67940

Other (OTH) AF: 0.511 AC: 1078 AN: 2110

Alfa AF: 0.516 Hom.: 11595

Bravo AF: 0.540

Asia WGS AF: 0.424 AC: 1476 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	0.064
DANN	Benign	0.46
PhyloP100		-1.4
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: rs7578650; hg19: chr2-125112975;