NM_021943.3:c.295+6869A>G

Variant names:

• chr6-38068644-A-G
• rs17589516
• NM_021943.3:c.295+6869A>G

Variant summary

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

The NM_021943.3(ZFAND3):​c.295+6869A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0655 in 152,288 control chromosomes in the GnomAD database, including 452 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 0.065 (452 hom., cov: 32)
• Consequence: ZFAND3 NM_021943.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.613
• Publications: 12 publications found

Genes affected

ZFAND3 (HGNC:18019): (zinc finger AN1-type containing 3) Predicted to enable DNA binding activity and zinc ion binding activity. [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=-0.84).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.093 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_021943.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ZFAND3	NM_021943.3	MANE Select	c.295+6869A>G		intron	N/A	NP_068762.1
	ZFAND3	NM_001410904.1		c.295+6869A>G		intron	N/A	NP_001397833.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ZFAND3	ENST00000287218.9	TSL:1 MANE Select	c.295+6869A>G		intron	N/A	ENSP00000287218.4
	ZFAND3	ENST00000373391.6	TSL:5	c.295+6869A>G		intron	N/A	ENSP00000362489.2
	ZFAND3	ENST00000474522.5	TSL:5	c.388+6869A>G		intron	N/A	ENSP00000420240.1

Frequencies

GnomAD3 genomes AF: 0.0656 AC: 9978 AN: 152170 Hom.: 453 Cov.: 32

Gnomad AFR AF: 0.0150

Gnomad AMI AF: 0.0581

Gnomad AMR AF: 0.0704

Gnomad ASJ AF: 0.160

Gnomad EAS AF: 0.00423

Gnomad SAS AF: 0.0644

Gnomad FIN AF: 0.0643

Gnomad MID AF: 0.101

Gnomad NFE AF: 0.0950

Gnomad OTH AF: 0.0784

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

GnomAD4 genome AF: 0.0655 AC: 9972 AN: 152288 Hom.: 452 Cov.: 32 AF XY: 0.0636 AC XY: 4734 AN XY: 74454

African (AFR) AF: 0.0150 AC: 622 AN: 41562

American (AMR) AF: 0.0703 AC: 1075 AN: 15296

Ashkenazi Jewish (ASJ) AF: 0.160 AC: 556 AN: 3466

East Asian (EAS) AF: 0.00424 AC: 22 AN: 5192

South Asian (SAS) AF: 0.0635 AC: 306 AN: 4822

European-Finnish (FIN) AF: 0.0643 AC: 682 AN: 10606

Middle Eastern (MID) AF: 0.102 AC: 30 AN: 294

European-Non Finnish (NFE) AF: 0.0950 AC: 6461 AN: 68024

Other (OTH) AF: 0.0781 AC: 165 AN: 2114

Alfa AF: 0.0889 Hom.: 1755

Bravo AF: 0.0624

Asia WGS AF: 0.0390 AC: 135 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.84
CADD	Benign	0.60
DANN	Benign	0.80
PhyloP100		-0.61
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs17589516; hg19: chr6-38036420;