chr19-35857688-C-G

Position:

• chr19-35857688-C-G

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_199180.4(KIRREL2):​c.211+194C>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0603 in 152,054 control chromosomes in the GnomAD database, including 829 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 0.060 (829 hom., cov: 31)
• Consequence: KIRREL2 NM_199180.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.46

Genes affected

KIRREL2 (HGNC:18816): (kirre like nephrin family adhesion molecule 2) This gene encodes a type I transmembrane protein and member of the immunoglobulin superfamily of cell adhesion molecules. The encoded protein localizes to adherens junctions in pancreatic beta cells and regulates insulin secretion. Autoantibodies against the encoded protein have been detected in serum from patients with type 1 diabetes. This gene may also play a role in glomerular development and decreased expression of this gene has been observed in human glomerular diseases. This gene and the related opposite-strand gene nephrin (GeneID: 527362) are regulated by a bidirectional promoter. [provided by RefSeq, Jul 2016]

NPHS1 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.194 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
KIRREL2	NM_199180.4	c.211+194C>G		intron_variant		ENST00000360202.10	NP_954649.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
KIRREL2	ENST00000360202.10	c.211+194C>G		intron_variant		1	NM_199180.4	ENSP00000353331.4

Frequencies

GnomAD3 genomes AF: 0.0603 AC: 9164 AN: 151936 Hom.: 826 Cov.: 31

Gnomad AFR AF: 0.198

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.0259

Gnomad ASJ AF: 0.0138

Gnomad EAS AF: 0.0639

Gnomad SAS AF: 0.00973

Gnomad FIN AF: 0.000473

Gnomad MID AF: 0.0285

Gnomad NFE AF: 0.00110

Gnomad OTH AF: 0.0429

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

GnomAD4 genome AF: 0.0603 AC: 9170 AN: 152054 Hom.: 829 Cov.: 31 AF XY: 0.0587 AC XY: 4364 AN XY: 74324

Gnomad4 AFR AF: 0.197

Gnomad4 AMR AF: 0.0259

Gnomad4 ASJ AF: 0.0138

Gnomad4 EAS AF: 0.0639

Gnomad4 SAS AF: 0.00954

Gnomad4 FIN AF: 0.000473

Gnomad4 NFE AF: 0.00110

Gnomad4 OTH AF: 0.0419

Alfa AF: 0.0351 Hom.: 59

Bravo AF: 0.0690

Asia WGS AF: 0.0350 AC: 121 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	0.14
DANN	Benign	0.50

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: rs670091; hg19: chr19-36348590;