rs1545240

Variant names:

• chr8-134630389-A-C
• rs1545240
• NM_020863.4:c.448+7072T>G

Your query was ambiguous. Multiple possible variants found:

• chr8-134630389-A-C
• chr8-134630389-A-G

Variant summary

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

The NM_020863.4(ZFAT):​c.448+7072T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.757 in 152,236 control chromosomes in the GnomAD database, including 43,884 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 0.76 (43884 hom., cov: 34)
• Consequence: ZFAT NM_020863.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.469
• Publications: 2 publications found

Genes affected

ZFAT (HGNC:19899): (zinc finger and AT-hook domain containing) This gene encodes a protein that likely binds DNA and functions as a transcriptional regulator involved in apoptosis and cell survival. This gene resides in a susceptibility locus for autoimmune thyroid disease (AITD) on chromosome 8q24. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Nov 2009]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.889 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ZFAT	NM_020863.4	c.448+7072T>G		intron_variant	Intron 3 of 15	ENST00000377838.8	NP_065914.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ZFAT	ENST00000377838.8	c.448+7072T>G		intron_variant	Intron 3 of 15	1	NM_020863.4	ENSP00000367069.3
ZFAT	ENST00000429442.6	c.412+7072T>G		intron_variant	Intron 3 of 15	1		ENSP00000394501.2

Frequencies

GnomAD3 genomes AF: 0.757 AC: 115100 AN: 152118 Hom.: 43840 Cov.: 34

Gnomad AFR AF: 0.781

Gnomad AMI AF: 0.661

Gnomad AMR AF: 0.801

Gnomad ASJ AF: 0.572

Gnomad EAS AF: 0.911

Gnomad SAS AF: 0.770

Gnomad FIN AF: 0.812

Gnomad MID AF: 0.684

Gnomad NFE AF: 0.722

Gnomad OTH AF: 0.750

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

GnomAD4 genome AF: 0.757 AC: 115198 AN: 152236 Hom.: 43884 Cov.: 34 AF XY: 0.762 AC XY: 56732 AN XY: 74418

African (AFR) AF: 0.781 AC: 32411 AN: 41520

American (AMR) AF: 0.801 AC: 12257 AN: 15302

Ashkenazi Jewish (ASJ) AF: 0.572 AC: 1983 AN: 3468

East Asian (EAS) AF: 0.911 AC: 4720 AN: 5182

South Asian (SAS) AF: 0.769 AC: 3716 AN: 4830

European-Finnish (FIN) AF: 0.812 AC: 8613 AN: 10604

Middle Eastern (MID) AF: 0.701 AC: 206 AN: 294

European-Non Finnish (NFE) AF: 0.722 AC: 49106 AN: 68018

Other (OTH) AF: 0.752 AC: 1583 AN: 2106

Alfa AF: 0.717 Hom.: 3946

Bravo AF: 0.759

Asia WGS AF: 0.811 AC: 2823 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	8.5
DANN	Benign	0.83
PhyloP100		0.47
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: rs1545240; hg19: chr8-135642632;