rs1725854

Variant names:

• chr12-77660661-G-C
• rs1725854
• ENST00000550042.2:c.72+88395G>C

Variant summary

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

The ENST00000550042.2(NAV3):​c.72+88395G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.181 in 151,958 control chromosomes in the GnomAD database, including 3,319 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 0.18 (3319 hom., cov: 32)
• Consequence: NAV3 ENST00000550042.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.30

Genes affected

NAV3 (HGNC:15998): (neuron navigator 3) This gene belongs to the neuron navigator family and is expressed predominantly in the nervous system. The encoded protein contains coiled-coil domains and a conserved AAA domain characteristic for ATPases associated with a variety of cellular activities. This gene is similar to unc-53, a Caenorhabditis elegans gene involved in axon guidance. Multiple alternatively spliced transcript variants for this gene have been described but only one has had its full-length nature determined. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.96).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.334 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
NAV3	XM_017020166.3	c.72+88395G>C		intron_variant	Intron 1 of 39		XP_016875655.1
NAV3	XM_017020167.1	c.72+88395G>C		intron_variant	Intron 1 of 38		XP_016875656.1
NAV3	XM_047429817.1	c.72+88395G>C		intron_variant	Intron 1 of 37		XP_047285773.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
NAV3	ENST00000550042.2	c.72+88395G>C		intron_variant	Intron 2 of 8	5		ENSP00000489639.1

Frequencies

GnomAD3 genomes AF: 0.181 AC: 27470 AN: 151840 Hom.: 3303 Cov.: 32

Gnomad AFR AF: 0.339

Gnomad AMI AF: 0.0286

Gnomad AMR AF: 0.162

Gnomad ASJ AF: 0.160

Gnomad EAS AF: 0.0593

Gnomad SAS AF: 0.111

Gnomad FIN AF: 0.200

Gnomad MID AF: 0.218

Gnomad NFE AF: 0.103

Gnomad OTH AF: 0.181

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

GnomAD4 genome AF: 0.181 AC: 27527 AN: 151958 Hom.: 3319 Cov.: 32 AF XY: 0.183 AC XY: 13597 AN XY: 74282

Gnomad4 AFR AF: 0.339

Gnomad4 AMR AF: 0.162

Gnomad4 ASJ AF: 0.160

Gnomad4 EAS AF: 0.0595

Gnomad4 SAS AF: 0.111

Gnomad4 FIN AF: 0.200

Gnomad4 NFE AF: 0.103

Gnomad4 OTH AF: 0.186

Alfa AF: 0.151 Hom.: 275

Bravo AF: 0.187

Asia WGS AF: 0.121 AC: 424 AN: 3474

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.96
CADD	Benign	0.13
DANN	Benign	0.59

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs1725854; hg19: chr12-78054441;