rs6755404

Variant names:

• chr2-184932501-A-C
• rs6755404
• NM_194250.2:c.256-1102A>C

Your query was ambiguous. Multiple possible variants found:

• chr2-184932501-A-C
• chr2-184932501-A-G
• chr2-184932501-A-T

Variant summary

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

The NM_194250.2(ZNF804A):​c.256-1102A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.823 in 151,994 control chromosomes in the GnomAD database, including 51,791 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 0.82 (51791 hom., cov: 30)
• Consequence: ZNF804A NM_194250.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.639
• Publications: 13 publications found

Genes affected

ZNF804A (HGNC:21711): (zinc finger protein 804A) The protein encoded by this gene is a zinc finger binding protein. Polymorphisms in this gene, especially rs1344706, are thought to confer increased susceptibility to schizophrenia, bipolar disorder, and heroin addiciton. [provided by RefSeq, Nov 2015]

ZNF804A Gene-Disease associations (from GenCC):

• complex neurodevelopmental disorder

  Inheritance: AD Classification: LIMITED Submitted by: Ambry Genetics

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 = 0.879 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_194250.2. 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
	ZNF804A	NM_194250.2	MANE Select	c.256-1102A>C		intron	N/A	NP_919226.1	Q7Z570

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ZNF804A	ENST00000302277.7	TSL:1 MANE Select	c.256-1102A>C		intron	N/A	ENSP00000303252.6	Q7Z570

Frequencies

GnomAD3 genomes AF: 0.823 AC: 125045 AN: 151876 Hom.: 51759 Cov.: 30

Gnomad AFR AF: 0.886

Gnomad AMI AF: 0.618

Gnomad AMR AF: 0.863

Gnomad ASJ AF: 0.873

Gnomad EAS AF: 0.871

Gnomad SAS AF: 0.738

Gnomad FIN AF: 0.757

Gnomad MID AF: 0.861

Gnomad NFE AF: 0.788

Gnomad OTH AF: 0.838

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

GnomAD4 genome AF: 0.823 AC: 125129 AN: 151994 Hom.: 51791 Cov.: 30 AF XY: 0.822 AC XY: 61016 AN XY: 74258

African (AFR) AF: 0.886 AC: 36754 AN: 41470

American (AMR) AF: 0.863 AC: 13185 AN: 15282

Ashkenazi Jewish (ASJ) AF: 0.873 AC: 3031 AN: 3470

East Asian (EAS) AF: 0.871 AC: 4473 AN: 5134

South Asian (SAS) AF: 0.738 AC: 3546 AN: 4802

European-Finnish (FIN) AF: 0.757 AC: 7995 AN: 10556

Middle Eastern (MID) AF: 0.878 AC: 258 AN: 294

European-Non Finnish (NFE) AF: 0.788 AC: 53575 AN: 67964

Other (OTH) AF: 0.828 AC: 1748 AN: 2110

Alfa AF: 0.811 Hom.: 7910

Bravo AF: 0.836

Asia WGS AF: 0.773 AC: 2690 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	0.88
DANN	Benign	0.53
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: rs6755404; hg19: chr2-185797228;