rs1317625

Variant names:

• chr18-48853811-G-A
• rs1317625
• NM_014772.3:c.1528-3777G>A

Variant summary

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

The NM_014772.3(CTIF):​c.1528-3777G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.296 in 152,076 control chromosomes in the GnomAD database, including 8,022 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 0.30 (8022 hom., cov: 32)
• Consequence: CTIF NM_014772.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.904
• Publications: 6 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]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.498 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_014772.3. 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
	CTIF	NM_014772.3	MANE Select	c.1528-3777G>A		intron	N/A	NP_055587.1	O43310-1
	CTIF	NM_001142397.2		c.1534-3777G>A		intron	N/A	NP_001135869.1	O43310-2

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CTIF	ENST00000256413.8	TSL:1 MANE Select	c.1528-3777G>A		intron	N/A	ENSP00000256413.3	O43310-1
	CTIF	ENST00000382998.8	TSL:1	c.1534-3777G>A		intron	N/A	ENSP00000372459.3	O43310-2
	CTIF	ENST00000865538.1		c.1582-3777G>A		intron	N/A	ENSP00000535597.1

Frequencies

GnomAD3 genomes AF: 0.296 AC: 44942 AN: 151958 Hom.: 7999 Cov.: 32

Gnomad AFR AF: 0.504

Gnomad AMI AF: 0.296

Gnomad AMR AF: 0.204

Gnomad ASJ AF: 0.211

Gnomad EAS AF: 0.0529

Gnomad SAS AF: 0.297

Gnomad FIN AF: 0.196

Gnomad MID AF: 0.259

Gnomad NFE AF: 0.228

Gnomad OTH AF: 0.289

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

GnomAD4 genome AF: 0.296 AC: 45003 AN: 152076 Hom.: 8022 Cov.: 32 AF XY: 0.292 AC XY: 21696 AN XY: 74350

African (AFR) AF: 0.504 AC: 20890 AN: 41444

American (AMR) AF: 0.204 AC: 3112 AN: 15288

Ashkenazi Jewish (ASJ) AF: 0.211 AC: 733 AN: 3470

East Asian (EAS) AF: 0.0528 AC: 273 AN: 5170

South Asian (SAS) AF: 0.297 AC: 1432 AN: 4814

European-Finnish (FIN) AF: 0.196 AC: 2079 AN: 10596

Middle Eastern (MID) AF: 0.252 AC: 74 AN: 294

European-Non Finnish (NFE) AF: 0.228 AC: 15533 AN: 67982

Other (OTH) AF: 0.288 AC: 607 AN: 2106

Alfa AF: 0.246 Hom.: 22829

Bravo AF: 0.301

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	0.049
DANN	Benign	0.62
PhyloP100		-0.90
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: rs1317625; hg19: chr18-46380182;