NM_018664.3:c.195+767G>T

Variant names:

• chr1-212696194-C-A
• rs1156058
• NM_018664.3:c.195+767G>T

Variant summary

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

The NM_018664.3(BATF3):​c.195+767G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.628 in 151,654 control chromosomes in the GnomAD database, including 30,299 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 0.63 (30299 hom., cov: 30)
• Consequence: BATF3 NM_018664.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.644
• Publications: 8 publications found

Genes affected

BATF3 (HGNC:28915): (basic leucine zipper ATF-like transcription factor 3) This gene encodes a member of the basic leucine zipper protein family. The encoded protein functions as a transcriptional repressor when heterodimerizing with JUN. The protein may play a role in repression of interleukin-2 and matrix metalloproteinase-1 transcription.[provided by RefSeq, Feb 2009]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.98).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.655 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_018664.3. 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
	BATF3	NM_018664.3	MANE Select	c.195+767G>T		intron	N/A	NP_061134.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	BATF3	ENST00000243440.2	TSL:1 MANE Select	c.195+767G>T		intron	N/A	ENSP00000243440.1
	BATF3	ENST00000478275.1	TSL:2	n.1795+767G>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.628 AC: 95210 AN: 151560 Hom.: 30274 Cov.: 30

Gnomad AFR AF: 0.609

Gnomad AMI AF: 0.598

Gnomad AMR AF: 0.470

Gnomad ASJ AF: 0.609

Gnomad EAS AF: 0.642

Gnomad SAS AF: 0.670

Gnomad FIN AF: 0.713

Gnomad MID AF: 0.674

Gnomad NFE AF: 0.660

Gnomad OTH AF: 0.613

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

GnomAD4 genome AF: 0.628 AC: 95260 AN: 151654 Hom.: 30299 Cov.: 30 AF XY: 0.630 AC XY: 46635 AN XY: 74082

African (AFR) AF: 0.609 AC: 25176 AN: 41310

American (AMR) AF: 0.469 AC: 7133 AN: 15216

Ashkenazi Jewish (ASJ) AF: 0.609 AC: 2112 AN: 3466

East Asian (EAS) AF: 0.642 AC: 3327 AN: 5180

South Asian (SAS) AF: 0.670 AC: 3206 AN: 4786

European-Finnish (FIN) AF: 0.713 AC: 7480 AN: 10492

Middle Eastern (MID) AF: 0.673 AC: 198 AN: 294

European-Non Finnish (NFE) AF: 0.660 AC: 44811 AN: 67906

Other (OTH) AF: 0.608 AC: 1274 AN: 2096

Alfa AF: 0.642 Hom.: 60189

Bravo AF: 0.603

Asia WGS AF: 0.588 AC: 2046 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.98
CADD	Benign	5.7
DANN	Benign	0.63
PhyloP100		0.64
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: rs1156058; hg19: chr1-212869536;