NM_014772.3:c.1527+15277C>T

Variant names:

• chr18-48832653-C-T
• rs1319946
• NM_014772.3:c.1527+15277C>T

Variant summary

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

The NM_014772.3(CTIF):​c.1527+15277C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.483 in 152,044 control chromosomes in the GnomAD database, including 18,681 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 0.48 (18681 hom., cov: 32)
• Consequence: CTIF NM_014772.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.223
• Publications: 9 publications found

Genes affected

CTIF (HGNC:23925): (cap binding complex dependent translation initiation factor) CTIF is a component of the CBP80 (NCBP1; MIM 600469)/CBP20 (NCBP2; MIM 605133) translation initiation complex that binds cotranscriptionally to the cap end of nascent mRNA. The CBP80/CBP20 complex is involved in a simultaneous editing and translation step that recognizes premature termination codons (PTCs) in mRNAs and directs PTC-containing mRNAs toward nonsense-mediated decay (NMD). On mRNAs without PTCs, the CBP80/CBP20 complex is replaced with cytoplasmic mRNA cap-binding proteins, including EIF4G (MIM 600495), and steady-state translation of the mRNAs resumes in the cytoplasm (Kim et al., 2009 [PubMed 19648179]).[supplied by OMIM, Dec 2009]

CTIF-AS1 (HGNC:58323):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.72).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.676 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CTIF	NM_014772.3	c.1527+15277C>T		intron_variant	Intron 10 of 11	ENST00000256413.8	NP_055587.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CTIF	ENST00000256413.8	c.1527+15277C>T		intron_variant	Intron 10 of 11	1	NM_014772.3	ENSP00000256413.3

Frequencies

GnomAD3 genomes AF: 0.483 AC: 73412 AN: 151926 Hom.: 18664 Cov.: 32

Gnomad AFR AF: 0.324

Gnomad AMI AF: 0.557

Gnomad AMR AF: 0.609

Gnomad ASJ AF: 0.595

Gnomad EAS AF: 0.655

Gnomad SAS AF: 0.695

Gnomad FIN AF: 0.475

Gnomad MID AF: 0.680

Gnomad NFE AF: 0.516

Gnomad OTH AF: 0.520

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

GnomAD4 genome AF: 0.483 AC: 73463 AN: 152044 Hom.: 18681 Cov.: 32 AF XY: 0.488 AC XY: 36238 AN XY: 74300

African (AFR) AF: 0.324 AC: 13433 AN: 41454

American (AMR) AF: 0.610 AC: 9323 AN: 15292

Ashkenazi Jewish (ASJ) AF: 0.595 AC: 2065 AN: 3470

East Asian (EAS) AF: 0.656 AC: 3389 AN: 5170

South Asian (SAS) AF: 0.695 AC: 3352 AN: 4820

European-Finnish (FIN) AF: 0.475 AC: 5015 AN: 10558

Middle Eastern (MID) AF: 0.677 AC: 199 AN: 294

European-Non Finnish (NFE) AF: 0.516 AC: 35086 AN: 67962

Other (OTH) AF: 0.518 AC: 1093 AN: 2112

Alfa AF: 0.518 Hom.: 40430

Bravo AF: 0.485

Asia WGS AF: 0.655 AC: 2279 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.72
CADD	Benign	7.5
DANN	Benign	0.59
PhyloP100		0.22
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: rs1319946; hg19: chr18-46359024;