rs7115136

Positions:

• chr11-99064473-A-G

Variant summary

Our verdict is Benign. Variant got -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

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

Verdict is Benign. Variant got -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.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
CNTN5	NM_014361.4	c.-210+43203A>G		intron_variant		ENST00000524871.6	NP_055176.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
CNTN5	ENST00000524871.6	c.-210+43203A>G		intron_variant		1	NM_014361.4	ENSP00000435637	P1
CNTN5	ENST00000527185.5	c.-210+43203A>G		intron_variant		1		ENSP00000433575
CNTN5	ENST00000528727.5	n.295+43203A>G		intron_variant, non_coding_transcript_variant		1
CNTN5	ENST00000528682.5	c.-71+43203A>G		intron_variant		5		ENSP00000436185	P1

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

Gnomad4 AFR AF: 0.427

Gnomad4 AMR AF: 0.308

Gnomad4 ASJ AF: 0.314

Gnomad4 EAS AF: 0.0866

Gnomad4 SAS AF: 0.392

Gnomad4 FIN AF: 0.278

Gnomad4 NFE AF: 0.316

Gnomad4 OTH AF: 0.367

Alfa AF: 0.326 Hom.: 6551

Bravo AF: 0.343

Asia WGS AF: 0.302 AC: 1047 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.84
CADD	Benign	12
DANN	Benign	0.85

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

Publications

LitVar

Other links and lift over

dbSNP: rs7115136; hg19: chr11-98935203;