rs10854142

Positions:

• chr19-9302780-A-G

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_198535.3(ZNF699):​c.49-276T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.592 in 152,034 control chromosomes in the GnomAD database, including 26,873 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 0.59 (26873 hom., cov: 32)
• Consequence: ZNF699 NM_198535.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.529

Genes affected

ZNF699 (HGNC:24750): (zinc finger protein 699) Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.0).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.643 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
ZNF699	NM_198535.3	c.49-276T>C		intron_variant		ENST00000591998.6	NP_940937.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
ZNF699	ENST00000591998.6	c.49-276T>C		intron_variant		5	NM_198535.3	ENSP00000467723	P1
ZNF699	ENST00000308650.4	c.49-276T>C		intron_variant		1		ENSP00000311596	P1
ZNF699	ENST00000588336.1	n.490-276T>C		intron_variant, non_coding_transcript_variant		4

Frequencies

GnomAD3 genomes AF: 0.592 AC: 89929 AN: 151916 Hom.: 26844 Cov.: 32

Gnomad AFR AF: 0.649

Gnomad AMI AF: 0.488

Gnomad AMR AF: 0.573

Gnomad ASJ AF: 0.663

Gnomad EAS AF: 0.475

Gnomad SAS AF: 0.589

Gnomad FIN AF: 0.453

Gnomad MID AF: 0.652

Gnomad NFE AF: 0.588

Gnomad OTH AF: 0.622

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

GnomAD4 genome AF: 0.592 AC: 90013 AN: 152034 Hom.: 26873 Cov.: 32 AF XY: 0.586 AC XY: 43530 AN XY: 74336

Gnomad4 AFR AF: 0.650

Gnomad4 AMR AF: 0.573

Gnomad4 ASJ AF: 0.663

Gnomad4 EAS AF: 0.475

Gnomad4 SAS AF: 0.589

Gnomad4 FIN AF: 0.453

Gnomad4 NFE AF: 0.588

Gnomad4 OTH AF: 0.618

Alfa AF: 0.343 Hom.: 601

Bravo AF: 0.604

Asia WGS AF: 0.544 AC: 1897 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	1.5
DANN	Benign	0.53

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

Publications

LitVar

Other links and lift over

dbSNP: rs10854142; hg19: chr19-9413456;