rs754046046

Variant names:

• chr20-43637268-CTTT-C
• NM_016004.5:c.1120+24_1120+26delTTT

Your query was ambiguous. Multiple possible variants found:

• chr20-43637268-CTTT-C
• chr20-43637268-CTTT-CT
• chr20-43637268-CTTT-CTT
• chr20-43637268-CTTT-CTTTT
• chr20-43637268-CTTT-CTTTTT
• chr20-43637268-CTTT-CTTTTTT

Variant summary

Our verdict is Uncertain significance. Variant got 2 ACMG points: 2P and 0B. PM2

The NM_016004.5(IFT52):​c.1120+24_1120+26delTTT variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000192 in 1,040,532 control chromosomes in the GnomAD database, with no homozygous occurrence. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: not found (cov: 33)
  • Exomes 𝑓: 0.0000019 (0 hom.)
• Consequence: IFT52 NM_016004.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.27

Genes affected

IFT52 (HGNC:15901): (intraflagellar transport 52) This gene encodes a conserved proline-rich protein that is a component of the intraflagellar transport-B (IFT-B) core complex. The encoded protein is essential for the integrity of the IFT-B core complex, and for biosynthesis and maintenance of cilia. Mutations in this gene are associated with ciliopathy that affects the skeleton. [provided by RefSeq, Oct 2016]

ACMG classification

Verdict is Uncertain_significance. Variant got 2 ACMG points.

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

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
IFT52	NM_016004.5	c.1120+24_1120+26delTTT		intron_variant	Intron 12 of 13	ENST00000373030.8	NP_057088.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
IFT52	ENST00000373030.8	c.1120+16_1120+18delTTT		intron_variant	Intron 12 of 13	1	NM_016004.5	ENSP00000362121.3
IFT52	ENST00000373039.4	c.1120+16_1120+18delTTT		intron_variant	Intron 12 of 13	5		ENSP00000362130.4
IFT52	ENST00000461012.1	n.107+16_107+18delTTT		intron_variant	Intron 1 of 1	2
IFT52	ENST00000468420.5	n.*65_*67delTTT		downstream_gene_variant		5

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome AF: 0.00000192 AC: 2 AN: 1040532 Hom.: 0 AF XY: 0.00000388 AC XY: 2 AN XY: 515486

Gnomad4 AFR exome AF: 0.00

Gnomad4 AMR exome AF: 0.00

Gnomad4 ASJ exome AF: 0.00

Gnomad4 EAS exome AF: 0.00

Gnomad4 SAS exome AF: 0.00

Gnomad4 FIN exome AF: 0.00

Gnomad4 NFE exome AF: 0.00000247

Gnomad4 OTH exome AF: 0.00

GnomAD4 genome Cov.: 33

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

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

No publications associated with this variant yet.

Other links and lift over

hg19: chr20-42265908;