chr11-126994498-G-T

Position:

• chr11-126994498-G-T

Variant summary

Our verdict is Benign. Variant got -10 ACMG points: 0P and 10B. BP4_Moderate BA1

The NM_032531.4(KIRREL3):​c.55+5957C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.204 in 152,178 control chromosomes in the GnomAD database, including 3,872 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 0.20 (3872 hom., cov: 32)
• Consequence: KIRREL3 NM_032531.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.72

Genes affected

KIRREL3 (HGNC:23204): (kirre like nephrin family adhesion molecule 3) The protein encoded by this gene is a member of the nephrin-like protein family. These proteins are expressed in fetal and adult brain, and also in podocytes of kidney glomeruli. The cytoplasmic domains of these proteins interact with the C-terminus of podocin, also expressed in the podocytes, cells involved in ensuring size- and charge-selective ultrafiltration. The protein encoded by this gene is a synaptic cell adhesion molecule with multiple extracellular immunoglobulin-like domains and a cytoplasmic PDZ domain-binding motif. Mutations in this gene are associated with several neurological and cognitive disorders. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]

KIRREL3 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -10 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.37).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.332 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
KIRREL3	NM_032531.4	c.55+5957C>A		intron_variant		ENST00000525144.7	NP_115920.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
KIRREL3	ENST00000525144.7	c.55+5957C>A		intron_variant		1	NM_032531.4	ENSP00000435466.2

Frequencies

GnomAD3 genomes AF: 0.204 AC: 31063 AN: 152060 Hom.: 3871 Cov.: 32

Gnomad AFR AF: 0.337

Gnomad AMI AF: 0.208

Gnomad AMR AF: 0.157

Gnomad ASJ AF: 0.286

Gnomad EAS AF: 0.00346

Gnomad SAS AF: 0.126

Gnomad FIN AF: 0.0970

Gnomad MID AF: 0.323

Gnomad NFE AF: 0.166

Gnomad OTH AF: 0.223

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

GnomAD4 genome AF: 0.204 AC: 31079 AN: 152178 Hom.: 3872 Cov.: 32 AF XY: 0.197 AC XY: 14684 AN XY: 74412

Gnomad4 AFR AF: 0.337

Gnomad4 AMR AF: 0.157

Gnomad4 ASJ AF: 0.286

Gnomad4 EAS AF: 0.00347

Gnomad4 SAS AF: 0.126

Gnomad4 FIN AF: 0.0970

Gnomad4 NFE AF: 0.166

Gnomad4 OTH AF: 0.220

Alfa AF: 0.118 Hom.: 303

Bravo AF: 0.219

Asia WGS AF: 0.0700 AC: 245 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.37
CADD	Benign	15
DANN	Benign	0.83

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: rs488054; hg19: chr11-126864394;