ENST00000616568.5:c.42+4168A>G

Variant names:

• chr9-120890620-T-C
• rs881375
• ENST00000616568.5:c.42+4168A>G

Variant summary

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

The ENST00000616568.5(PHF19):​c.42+4168A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.685 in 151,988 control chromosomes in the GnomAD database, including 35,924 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 0.68 (35924 hom., cov: 31)
• Consequence: PHF19 ENST00000616568.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0720
• Publications: 76 publications found

Genes affected

PHF19 (HGNC:24566): (PHD finger protein 19) Enables methylated histone binding activity. Involved in positive regulation of histone H3-K27 methylation. Colocalizes with ESC/E(Z) complex. [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=-0.48).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.776 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
PHF19	NM_001286840.1	c.42+4168A>G		intron_variant	Intron 1 of 14		NP_001273769.1
PHF19	XM_017014612.3	c.-16+11270A>G		intron_variant	Intron 1 of 14		XP_016870101.1
PHF19	XM_047423210.1	c.42+4168A>G		intron_variant	Intron 1 of 13		XP_047279166.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
PHF19	ENST00000616568.5	c.42+4168A>G		intron_variant	Intron 1 of 14	1		ENSP00000483946.1

Frequencies

GnomAD3 genomes AF: 0.685 AC: 104012 AN: 151870 Hom.: 35876 Cov.: 31

Gnomad AFR AF: 0.755

Gnomad AMI AF: 0.488

Gnomad AMR AF: 0.702

Gnomad ASJ AF: 0.743

Gnomad EAS AF: 0.720

Gnomad SAS AF: 0.797

Gnomad FIN AF: 0.576

Gnomad MID AF: 0.804

Gnomad NFE AF: 0.643

Gnomad OTH AF: 0.707

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

GnomAD4 genome AF: 0.685 AC: 104111 AN: 151988 Hom.: 35924 Cov.: 31 AF XY: 0.685 AC XY: 50883 AN XY: 74286

African (AFR) AF: 0.755 AC: 31317 AN: 41456

American (AMR) AF: 0.702 AC: 10721 AN: 15262

Ashkenazi Jewish (ASJ) AF: 0.743 AC: 2575 AN: 3468

East Asian (EAS) AF: 0.721 AC: 3726 AN: 5170

South Asian (SAS) AF: 0.797 AC: 3844 AN: 4824

European-Finnish (FIN) AF: 0.576 AC: 6078 AN: 10544

Middle Eastern (MID) AF: 0.799 AC: 235 AN: 294

European-Non Finnish (NFE) AF: 0.643 AC: 43685 AN: 67958

Other (OTH) AF: 0.707 AC: 1487 AN: 2104

Alfa AF: 0.670 Hom.: 148060

Bravo AF: 0.696

Asia WGS AF: 0.766 AC: 2662 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.48
CADD	Benign	16
DANN	Benign	0.65
PhyloP100		-0.072

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs881375; hg19: chr9-123652898;