rs7583934

Variant names:

• chr2-141147483-G-T
• rs7583934
• NM_018557.3:c.1013+40938C>A

Variant summary

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

The NM_018557.3(LRP1B):​c.1013+40938C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.678 in 152,000 control chromosomes in the GnomAD database, including 35,134 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 0.68 (35134 hom., cov: 33)
• Consequence: LRP1B NM_018557.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.408

Genes affected

LRP1B (HGNC:6693): (LDL receptor related protein 1B) This gene encodes a member of the low density lipoprotein (LDL) receptor family. These receptors play a wide variety of roles in normal cell function and development due to their interactions with multiple ligands. Disruption of this gene has been reported in several types of cancer. [provided by RefSeq, Jun 2016]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.01).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.702 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
LRP1B	NM_018557.3	c.1013+40938C>A		intron_variant	Intron 7 of 90	ENST00000389484.8	NP_061027.2
LRP1B	XM_017004341.2	c.623+40938C>A		intron_variant	Intron 7 of 90		XP_016859830.1
LRP1B	XM_047444771.1	c.1124+40938C>A		intron_variant	Intron 7 of 76		XP_047300727.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
LRP1B	ENST00000389484.8	c.1013+40938C>A		intron_variant	Intron 7 of 90	1	NM_018557.3	ENSP00000374135.3
LRP1B	ENST00000434794.1	c.206-165207C>A		intron_variant	Intron 2 of 13	2		ENSP00000413239.1

Frequencies

GnomAD3 genomes AF: 0.678 AC: 103023 AN: 151882 Hom.: 35106 Cov.: 33

Gnomad AFR AF: 0.660

Gnomad AMI AF: 0.758

Gnomad AMR AF: 0.673

Gnomad ASJ AF: 0.730

Gnomad EAS AF: 0.547

Gnomad SAS AF: 0.711

Gnomad FIN AF: 0.587

Gnomad MID AF: 0.832

Gnomad NFE AF: 0.707

Gnomad OTH AF: 0.692

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

GnomAD4 genome AF: 0.678 AC: 103100 AN: 152000 Hom.: 35134 Cov.: 33 AF XY: 0.672 AC XY: 49941 AN XY: 74290

Gnomad4 AFR AF: 0.660

Gnomad4 AMR AF: 0.673

Gnomad4 ASJ AF: 0.730

Gnomad4 EAS AF: 0.545

Gnomad4 SAS AF: 0.711

Gnomad4 FIN AF: 0.587

Gnomad4 NFE AF: 0.707

Gnomad4 OTH AF: 0.696

Alfa AF: 0.694 Hom.: 9523

Bravo AF: 0.684

Asia WGS AF: 0.674 AC: 2340 AN: 3474

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	2.8
DANN	Benign	0.42

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: rs7583934; hg19: chr2-141905052;