rs3745369

Variant names:

• chr19-7670589-G-A
• rs3745369
• NM_020415.4:c.*240G>A

Your query was ambiguous. Multiple possible variants found:

• chr19-7670589-G-A
• chr19-7670589-G-C

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_020415.4(RETN):​c.*240G>A variant causes a downstream gene change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. 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: not found (cov: 30)
  • Exomes 𝑓: 0.0 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: RETN NM_020415.4 downstream_gene
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.930
• Publications: 20 publications found

Genes affected

RETN (HGNC:20389): (resistin) This gene belongs to the family defined by the mouse resistin-like genes. The characteristic feature of this family is the C-terminal stretch of 10 cys residues with identical spacing. The mouse homolog of this protein is secreted by adipocytes, and may be the hormone potentially linking obesity to type II diabetes. The encoded protein also has an antimicrobial role in skin, displaying antibacterial activity against both Gram positive and Gram negative bacteria. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2020]

RETN Gene-Disease associations (from GenCC):

• diabetes mellitus, noninsulin-dependent

  Inheritance: AD Classification: LIMITED Submitted by: Ambry Genetics

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.78).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
RETN	NM_020415.4	c.*240G>A		downstream_gene_variant		ENST00000221515.6	NP_065148.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
RETN	ENST00000221515.6	c.*240G>A		downstream_gene_variant		1	NM_020415.4	ENSP00000221515.1
RETN	ENST00000381324.2	c.*240G>A		downstream_gene_variant		1		ENSP00000370725.2
RETN	ENST00000629642.1	c.*240G>A		downstream_gene_variant		5		ENSP00000485998.1

Frequencies

GnomAD3 genomes Cov.: 30

GnomAD4 exome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0 AN: 438518 Hom.: 0 AF XY: 0.00 AC XY: 0 AN XY: 228932

African (AFR) AF: 0.00 AC: 0 AN: 12020

American (AMR) AF: 0.00 AC: 0 AN: 17372

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 13274

East Asian (EAS) AF: 0.00 AC: 0 AN: 29572

South Asian (SAS) AF: 0.00 AC: 0 AN: 41108

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 28968

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 1890

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 269078

Other (OTH) AF: 0.00 AC: 0 AN: 25236

GnomAD4 genome Cov.: 30

Alfa AF: 0.00 Hom.: 2010

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.78
CADD	Benign	0.85
DANN	Benign	0.96
PhyloP100		-0.93

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs3745369; hg19: chr19-7735475;