rs10205816

Variant names:

• chr2-43817116-A-G
• rs10205816
• NM_022436.3:c.1650-2527T>C

Variant summary

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

The NM_022436.3(ABCG5):​c.1650-2527T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.387 in 152,108 control chromosomes in the GnomAD database, including 13,412 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 0.39 (13412 hom., cov: 33)
• Consequence: ABCG5 NM_022436.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.511

Genes affected

ABCG5 (HGNC:13886): (ATP binding cassette subfamily G member 5) The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the White subfamily. The protein encoded by this gene functions as a half-transporter to limit intestinal absorption and promote biliary excretion of sterols. It is expressed in a tissue-specific manner in the liver, colon, and intestine. This gene is tandemly arrayed on chromosome 2, in a head-to-head orientation with family member ABCG8. Mutations in this gene may contribute to sterol accumulation and atheroschlerosis, and have been observed in patients with sitosterolemia. [provided by RefSeq, Jul 2008]

DYNC2LI1 (HGNC:24595): (dynein cytoplasmic 2 light intermediate chain 1) This gene encodes a protein that is a component of the dynein-2 microtubule motor protein complex that plays a role in the retrograde transport of cargo in primary cilia via the intraflagellar transport system. This gene is ubiquitously expressed and its protein, which localizes to the axoneme and Golgi apparatus, interacts directly with the cytoplasmic dynein 2 heavy chain 1 protein to form part of the multi-protein dynein-2 complex. Mutations in this gene produce defects in the dynein-2 complex which result in several types of ciliopathy including short-rib thoracic dysplasia 15 with polydactyly (SRTD15). Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2017]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.0).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.625 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ABCG5	NM_022436.3	c.1650-2527T>C		intron_variant	Intron 11 of 12	ENST00000405322.8	NP_071881.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ABCG5	ENST00000405322.8	c.1650-2527T>C		intron_variant	Intron 11 of 12	1	NM_022436.3	ENSP00000384513.2
ABCG5	ENST00000486512.5	n.2171-2527T>C		intron_variant	Intron 7 of 8	1
ABCG5	ENST00000409962.1	n.1933-2527T>C		intron_variant	Intron 7 of 8	2
ABCG5	ENST00000644754.1	n.2034-2527T>C		intron_variant	Intron 8 of 9

Frequencies

GnomAD3 genomes AF: 0.387 AC: 58795 AN: 151990 Hom.: 13362 Cov.: 33

Gnomad AFR AF: 0.631

Gnomad AMI AF: 0.237

Gnomad AMR AF: 0.419

Gnomad ASJ AF: 0.306

Gnomad EAS AF: 0.105

Gnomad SAS AF: 0.378

Gnomad FIN AF: 0.270

Gnomad MID AF: 0.405

Gnomad NFE AF: 0.278

Gnomad OTH AF: 0.360

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

GnomAD4 genome AF: 0.387 AC: 58905 AN: 152108 Hom.: 13412 Cov.: 33 AF XY: 0.384 AC XY: 28573 AN XY: 74354

Gnomad4 AFR AF: 0.631

Gnomad4 AMR AF: 0.420

Gnomad4 ASJ AF: 0.306

Gnomad4 EAS AF: 0.105

Gnomad4 SAS AF: 0.376

Gnomad4 FIN AF: 0.270

Gnomad4 NFE AF: 0.279

Gnomad4 OTH AF: 0.362

Alfa AF: 0.312 Hom.: 7759

Bravo AF: 0.407

Asia WGS AF: 0.313 AC: 1090 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	6.8
DANN	Benign	0.50

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: rs10205816; hg19: chr2-44044255;