15-98704789-C-T

Position:

• chr15-98704789-C-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_000875.5(IGF1R):​c.95-2773C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.756 in 151,918 control chromosomes in the GnomAD database, including 44,056 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 0.76 (44056 hom., cov: 30)
• Consequence: IGF1R NM_000875.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.68

Genes affected

IGF1R (HGNC:5465): (insulin like growth factor 1 receptor) This receptor binds insulin-like growth factor with a high affinity. It has tyrosine kinase activity. The insulin-like growth factor I receptor plays a critical role in transformation events. Cleavage of the precursor generates alpha and beta subunits. It is highly overexpressed in most malignant tissues where it functions as an anti-apoptotic agent by enhancing cell survival. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.98).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.88 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
IGF1R	NM_000875.5	c.95-2773C>T		intron_variant		ENST00000650285.1	NP_000866.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
IGF1R	ENST00000650285.1	c.95-2773C>T		intron_variant			NM_000875.5	ENSP00000497069	P4
IGF1R	ENST00000559925.5	n.95-2773C>T		intron_variant, non_coding_transcript_variant		1
IGF1R	ENST00000649865.1	c.95-2773C>T		intron_variant				ENSP00000496919	A1

Frequencies

GnomAD3 genomes AF: 0.756 AC: 114690 AN: 151802 Hom.: 44013 Cov.: 30

Gnomad AFR AF: 0.887

Gnomad AMI AF: 0.645

Gnomad AMR AF: 0.749

Gnomad ASJ AF: 0.692

Gnomad EAS AF: 0.758

Gnomad SAS AF: 0.653

Gnomad FIN AF: 0.743

Gnomad MID AF: 0.709

Gnomad NFE AF: 0.692

Gnomad OTH AF: 0.730

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

GnomAD4 genome AF: 0.756 AC: 114784 AN: 151918 Hom.: 44056 Cov.: 30 AF XY: 0.753 AC XY: 55938 AN XY: 74258

Gnomad4 AFR AF: 0.887

Gnomad4 AMR AF: 0.749

Gnomad4 ASJ AF: 0.692

Gnomad4 EAS AF: 0.758

Gnomad4 SAS AF: 0.653

Gnomad4 FIN AF: 0.743

Gnomad4 NFE AF: 0.692

Gnomad4 OTH AF: 0.725

Alfa AF: 0.698 Hom.: 53987

Bravo AF: 0.765

Asia WGS AF: 0.691 AC: 2406 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.98
CADD	Benign	0.073
DANN	Benign	0.71

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

LitVar

Other links and lift over

dbSNP: rs4966014; hg19: chr15-99248018;