NM_001040443.3:c.769+24G>T

Variant names:

• chr13-49524240-G-T
• rs7332573
• NM_001040443.3:c.769+24G>T

Variant summary

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

The NM_001040443.3(PHF11):​c.769+24G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.101 in 1,556,822 control chromosomes in the GnomAD database, including 12,091 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 0.16 (2884 hom., cov: 31)
  • Exomes 𝑓: 0.095 (9207 hom.)
• Consequence: PHF11 NM_001040443.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0290
• Publications: 11 publications found

Genes affected

PHF11 (HGNC:17024): (PHD finger protein 11) This gene encodes a protein containing a PHD (plant homeodomain) type zinc finger. This gene has been identified in some studies as a candidate gene for asthma. Naturally-occurring readthrough transcription may occur from the upstream SETDB2 (SET domain bifurcated 2) gene to this locus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]

SETDB2-PHF11 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.94).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.329 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001040443.3. 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
	PHF11	NM_001040443.3	MANE Select	c.769+24G>T		intron	N/A	NP_001035533.1
	SETDB2-PHF11	NM_001320727.2		c.2251+24G>T		intron	N/A	NP_001307656.1
	PHF11	NM_001040444.3		c.652+24G>T		intron	N/A	NP_001035534.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PHF11	ENST00000378319.8	TSL:1 MANE Select	c.769+24G>T		intron	N/A	ENSP00000367570.3
	PHF11	ENST00000488958.5	TSL:1	c.652+24G>T		intron	N/A	ENSP00000417539.1
	PHF11	ENST00000465045.5	TSL:1	n.652+24G>T		intron	N/A	ENSP00000418630.1

Frequencies

GnomAD3 genomes AF: 0.157 AC: 23608 AN: 150206 Hom.: 2874 Cov.: 31

Gnomad AFR AF: 0.333

Gnomad AMI AF: 0.0474

Gnomad AMR AF: 0.0962

Gnomad ASJ AF: 0.0612

Gnomad EAS AF: 0.221

Gnomad SAS AF: 0.264

Gnomad FIN AF: 0.0749

Gnomad MID AF: 0.0710

Gnomad NFE AF: 0.0726

Gnomad OTH AF: 0.112

GnomAD2 exomes AF: 0.130 AC: 29685 AN: 227738 AF XY: 0.131

Gnomad AFR exome AF: 0.342

Gnomad AMR exome AF: 0.118

Gnomad ASJ exome AF: 0.0645

Gnomad EAS exome AF: 0.216

Gnomad FIN exome AF: 0.0804

Gnomad NFE exome AF: 0.0781

Gnomad OTH exome AF: 0.0990

GnomAD4 exome AF: 0.0949 AC: 133426 AN: 1406500 Hom.: 9207 Cov.: 24 AF XY: 0.0989 AC XY: 69397 AN XY: 701402

African (AFR) AF: 0.335 AC: 10398 AN: 31052

American (AMR) AF: 0.107 AC: 4227 AN: 39534

Ashkenazi Jewish (ASJ) AF: 0.0649 AC: 1646 AN: 25360

East Asian (EAS) AF: 0.233 AC: 8910 AN: 38210

South Asian (SAS) AF: 0.246 AC: 19938 AN: 80972

European-Finnish (FIN) AF: 0.0810 AC: 4241 AN: 52388

Middle Eastern (MID) AF: 0.0849 AC: 420 AN: 4948

European-Non Finnish (NFE) AF: 0.0720 AC: 77503 AN: 1075862

Other (OTH) AF: 0.106 AC: 6143 AN: 58174

GnomAD4 genome AF: 0.157 AC: 23669 AN: 150322 Hom.: 2884 Cov.: 31 AF XY: 0.159 AC XY: 11662 AN XY: 73214

African (AFR) AF: 0.333 AC: 13664 AN: 40990

American (AMR) AF: 0.0959 AC: 1442 AN: 15040

Ashkenazi Jewish (ASJ) AF: 0.0612 AC: 212 AN: 3464

East Asian (EAS) AF: 0.221 AC: 1130 AN: 5112

South Asian (SAS) AF: 0.264 AC: 1261 AN: 4770

European-Finnish (FIN) AF: 0.0749 AC: 748 AN: 9984

Middle Eastern (MID) AF: 0.0729 AC: 21 AN: 288

European-Non Finnish (NFE) AF: 0.0726 AC: 4916 AN: 67682

Other (OTH) AF: 0.111 AC: 232 AN: 2084

Alfa AF: 0.0847 Hom.: 1255

Bravo AF: 0.161

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
CADD	Benign	1.8
DANN	Benign	0.22
PhyloP100		0.029
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: rs7332573; hg19: chr13-50098376; COSMIC: COSV107432167; COSMIC: COSV107432167;