rs918835696

Variant names:

• chrX-120527062-CTTTT-C
• rs918835696
• NM_001079872.2:c.2593-210_2593-207delAAAA

Your query was ambiguous. Multiple possible variants found:

• chrX-120527062-CTTTT-C
• chrX-120527062-CTTTT-CT
• chrX-120527062-CTTTT-CTT
• chrX-120527062-CTTTT-CTTT
• chrX-120527062-CTTTT-CTTTTT
• chrX-120527062-CTTTT-CTTTTTT
• chrX-120527062-CTTTT-CTTTTTTT

Variant summary

Our verdict is Uncertain significance. The variant received 2 ACMG points: 2P and 0B. PM2

The NM_001079872.2(CUL4B):​c.2593-210_2593-207delAAAA variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000992 in 100,844 control chromosomes in the GnomAD database, with no homozygous occurrence. There are no hemizygote samples in GnomAD. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.0000099 (0 hom., 0 hem., cov: 21)
• Consequence: CUL4B NM_001079872.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.18
• Publications: 0 publications found

Genes affected

CUL4B (HGNC:2555): (cullin 4B) This gene is a member of the cullin family. The encoded protein forms a complex that functions as an E3 ubiquitin ligase and catalyzes the polyubiquitination of specific protein substrates in the cell. The protein interacts with a ring finger protein, and is required for the proteolysis of several regulators of DNA replication including chromatin licensing and DNA replication factor 1 and cyclin E. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

CUL4B Gene-Disease associations (from GenCC):

• X-linked intellectual disability, Cabezas type

  Inheritance: XL Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: ClinGen, G2P, Labcorp Genetics (formerly Invitae), Orphanet

ACMG classification

Our verdict: Uncertain_significance. The variant received 2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001079872.2. 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
	CUL4B	NM_001079872.2	MANE Select	c.2593-210_2593-207delAAAA		intron	N/A	NP_001073341.1	Q13620-1
	CUL4B	NM_003588.4		c.2647-210_2647-207delAAAA		intron	N/A	NP_003579.3
	CUL4B	NM_001330624.2		c.2608-210_2608-207delAAAA		intron	N/A	NP_001317553.1	K4DI93

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CUL4B	ENST00000371322.11	TSL:1 MANE Select	c.2593-210_2593-207delAAAA		intron	N/A	ENSP00000360373.5	Q13620-1
	CUL4B	ENST00000681206.1		c.2707-210_2707-207delAAAA		intron	N/A	ENSP00000505480.1	A0A7P0T954
	CUL4B	ENST00000680673.1		c.2647-210_2647-207delAAAA		intron	N/A	ENSP00000505084.1	Q13620-2

Frequencies

GnomAD3 genomes AF: 0.00000992 AC: 1 AN: 100844 Hom.: 0 Cov.: 21

Gnomad AFR AF: 0.00

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.00

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.00

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.0000204

Gnomad OTH AF: 0.00

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

GnomAD4 genome AF: 0.00000992 AC: 1 AN: 100844 Hom.: 0 Cov.: 21 AF XY: 0.00 AC XY: 0 AN XY: 27712

⚠️ The allele balance in gnomAD version 4 Genomes is significantly skewed from the expected value of 0.5.

African (AFR) AF: 0.00 AC: 0 AN: 28126

American (AMR) AF: 0.00 AC: 0 AN: 9335

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 2443

East Asian (EAS) AF: 0.00 AC: 0 AN: 3304

South Asian (SAS) AF: 0.00 AC: 0 AN: 2354

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 4096

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 212

European-Non Finnish (NFE) AF: 0.0000204 AC: 1 AN: 49024

Other (OTH) AF: 0.00 AC: 0 AN: 1318

⚠️ The allele balance in gnomAD version 4 Genomes is significantly skewed from the expected value of 0.5. (p-value = 0), which strongly suggests a high chance of mosaicism in these individuals.

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
PhyloP100		1.2
Mutation Taster		=100/0	polymorphism

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: rs918835696; hg19: chrX-119660917;