chr19-58488906-A-G

Variant names:

• chr19-58488906-A-G
• rs4801273
• ENST00000864562.1:c.*22-8101T>C

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001304453.1(ZNF446):​c.803-384A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.503 in 150,354 control chromosomes in the GnomAD database, including 19,882 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 0.50 (19882 hom., cov: 28)
• Consequence: ZNF446 NM_001304453.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.840
• Publications: 19 publications found

Genes affected

SLC27A5 (HGNC:10999): (solute carrier family 27 member 5) The protein encoded by this gene is an isozyme of very long-chain acyl-CoA synthetase (VLCS). It is capable of activating very long-chain fatty-acids containing 24- and 26-carbons. It is expressed in liver and associated with endoplasmic reticulum but not with peroxisomes. Its primary role is in fatty acid elongation or complex lipid synthesis rather than in degradation. This gene has a mouse ortholog. [provided by RefSeq, Jul 2008]

ZNF446 (HGNC:21036): (zinc finger protein 446) Enables identical protein binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in extracellular space. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.02).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.65 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001304453.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ZNF446	NM_001304453.1		c.803-384A>G		intron	N/A	NP_001291382.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SLC27A5	ENST00000864562.1		c.*22-8101T>C		intron	N/A	ENSP00000534621.1
	SLC27A5	ENST00000864563.1		c.*22-5264T>C		intron	N/A	ENSP00000534622.1
	SLC27A5	ENST00000595851.5	TSL:2	n.*22-5260T>C		intron	N/A	ENSP00000469512.1	M0R075

Frequencies

GnomAD3 genomes AF: 0.503 AC: 75566 AN: 150236 Hom.: 19857 Cov.: 28

Gnomad AFR AF: 0.656

Gnomad AMI AF: 0.602

Gnomad AMR AF: 0.390

Gnomad ASJ AF: 0.389

Gnomad EAS AF: 0.288

Gnomad SAS AF: 0.372

Gnomad FIN AF: 0.511

Gnomad MID AF: 0.332

Gnomad NFE AF: 0.468

Gnomad OTH AF: 0.449

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

GnomAD4 genome AF: 0.503 AC: 75633 AN: 150354 Hom.: 19882 Cov.: 28 AF XY: 0.497 AC XY: 36475 AN XY: 73344

African (AFR) AF: 0.656 AC: 26693 AN: 40676

American (AMR) AF: 0.389 AC: 5859 AN: 15058

Ashkenazi Jewish (ASJ) AF: 0.389 AC: 1346 AN: 3464

East Asian (EAS) AF: 0.289 AC: 1483 AN: 5136

South Asian (SAS) AF: 0.371 AC: 1783 AN: 4800

European-Finnish (FIN) AF: 0.511 AC: 5161 AN: 10102

Middle Eastern (MID) AF: 0.338 AC: 98 AN: 290

European-Non Finnish (NFE) AF: 0.468 AC: 31729 AN: 67830

Other (OTH) AF: 0.447 AC: 932 AN: 2086

Alfa AF: 0.469 Hom.: 25963

Bravo AF: 0.503

Asia WGS AF: 0.401 AC: 1395 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	1.3
DANN	Benign	0.64
PhyloP100		-0.84

Splicing

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

Other links and lift over

dbSNP: rs4801273; hg19: chr19-59000273;