rs7115136

Variant names:

• chr11-99064473-A-G
• rs7115136
• NM_014361.4:c.-210+43203A>G

Variant summary

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

The NM_014361.4(CNTN5):​c.-210+43203A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.338 in 152,004 control chromosomes in the GnomAD database, including 9,166 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 0.34 (9166 hom., cov: 32)
• Consequence: CNTN5 NM_014361.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 2.83
• Publications: 7 publications found

Genes affected

CNTN5 (HGNC:2175): (contactin 5) The protein encoded by this gene is a member of the immunoglobulin superfamily, and contactin family, which mediate cell surface interactions during nervous system development. This protein is a glycosylphosphatidylinositol (GPI)-anchored neuronal membrane protein that functions as a cell adhesion molecule. It may play a role in the formation of axon connections in the developing nervous system. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.84).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.422 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_014361.4. 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
	CNTN5	NM_014361.4	MANE Select	c.-210+43203A>G		intron	N/A	NP_055176.1	O94779-1
	CNTN5	NM_001243270.2		c.-71+43203A>G		intron	N/A	NP_001230199.1	O94779-1
	CNTN5	NM_001243271.2		c.-210+43203A>G		intron	N/A	NP_001230200.1	O94779-4

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CNTN5	ENST00000524871.6	TSL:1 MANE Select	c.-210+43203A>G		intron	N/A	ENSP00000435637.1	O94779-1
	CNTN5	ENST00000527185.5	TSL:1	c.-210+43203A>G		intron	N/A	ENSP00000433575.1	O94779-4
	CNTN5	ENST00000528727.5	TSL:1	n.295+43203A>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.338 AC: 51371 AN: 151886 Hom.: 9153 Cov.: 32

Gnomad AFR AF: 0.427

Gnomad AMI AF: 0.301

Gnomad AMR AF: 0.309

Gnomad ASJ AF: 0.314

Gnomad EAS AF: 0.0870

Gnomad SAS AF: 0.392

Gnomad FIN AF: 0.278

Gnomad MID AF: 0.380

Gnomad NFE AF: 0.316

Gnomad OTH AF: 0.362

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

GnomAD4 genome AF: 0.338 AC: 51419 AN: 152004 Hom.: 9166 Cov.: 32 AF XY: 0.335 AC XY: 24926 AN XY: 74298

African (AFR) AF: 0.427 AC: 17708 AN: 41442

American (AMR) AF: 0.308 AC: 4701 AN: 15268

Ashkenazi Jewish (ASJ) AF: 0.314 AC: 1091 AN: 3472

East Asian (EAS) AF: 0.0866 AC: 449 AN: 5184

South Asian (SAS) AF: 0.392 AC: 1892 AN: 4822

European-Finnish (FIN) AF: 0.278 AC: 2943 AN: 10588

Middle Eastern (MID) AF: 0.361 AC: 106 AN: 294

European-Non Finnish (NFE) AF: 0.316 AC: 21481 AN: 67914

Other (OTH) AF: 0.367 AC: 774 AN: 2110

Alfa AF: 0.327 Hom.: 8021

Bravo AF: 0.343

Asia WGS AF: 0.302 AC: 1047 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.84
CADD	Benign	12
DANN	Benign	0.85
PhyloP100		2.8
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: rs7115136; hg19: chr11-98935203;