chr1-25543670-G-T

Variant names:

• chr1-25543670-G-T
• rs1378657299
• NM_015627.3:c.-29G>T

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_015627.3(LDLRAP1):​c.-29G>T variant causes a 5 prime UTR premature start codon gain change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000000946 in 1,056,850 control chromosomes in the GnomAD database, with no homozygous occurrence. 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: not found (cov: 32)
  • Exomes 𝑓: 9.5e-7 (0 hom.)
• Consequence: LDLRAP1 NM_015627.3 5_prime_UTR_premature_start_codon_gain
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.775
• Publications: 0 publications found

Genes affected

LDLRAP1 (HGNC:18640): (low density lipoprotein receptor adaptor protein 1) The protein encoded by this gene is a cytosolic protein which contains a phosphotyrosine binding (PTD) domain. The PTD domain has been found to interact with the cytoplasmic tail of the LDL receptor. Mutations in this gene lead to LDL receptor malfunction and cause the disorder autosomal recessive hypercholesterolaemia. [provided by RefSeq, Jul 2008]

LDLRAP1 Gene-Disease associations (from GenCC):

• hypercholesterolemia, familial, 4

  Inheritance: AR Classification: DEFINITIVE, STRONG Submitted by: ClinGen, Genomics England PanelApp, Labcorp Genetics (formerly Invitae)
• homozygous familial hypercholesterolemia

  Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.58).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_015627.3. 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
	LDLRAP1	NM_015627.3	MANE Select	c.-29G>T		5_prime_UTR_premature_start_codon_gain	Exon 1 of 9	NP_056442.2	Q5SW96
	LDLRAP1	NM_015627.3	MANE Select	c.-29G>T		5_prime_UTR	Exon 1 of 9	NP_056442.2	Q5SW96

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LDLRAP1	ENST00000374338.5	TSL:1 MANE Select	c.-29G>T		5_prime_UTR_premature_start_codon_gain	Exon 1 of 9	ENSP00000363458.4	Q5SW96
	LDLRAP1	ENST00000374338.5	TSL:1 MANE Select	c.-29G>T		5_prime_UTR	Exon 1 of 9	ENSP00000363458.4	Q5SW96
	LDLRAP1	ENST00000894925.1		c.-29G>T		5_prime_UTR_premature_start_codon_gain	Exon 1 of 10	ENSP00000564984.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome AF: 9.46e-7 AC: 1 AN: 1056850 Hom.: 0 Cov.: 27 AF XY: 0.00 AC XY: 0 AN XY: 500248

African (AFR) AF: 0.00 AC: 0 AN: 21938

American (AMR) AF: 0.00 AC: 0 AN: 7618

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 13058

East Asian (EAS) AF: 0.00 AC: 0 AN: 24700

South Asian (SAS) AF: 0.00 AC: 0 AN: 19524

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 20638

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 3104

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 904496

Other (OTH) AF: 0.0000239 AC: 1 AN: 41774

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.58
CADD	Benign	13
DANN	Benign	0.90
PhyloP100		0.78
PromoterAI		-0.078	Neutral
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		2.1

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: rs1378657299; hg19: chr1-25870161;