rs1750996

chr13-95159345-A-Gchr13-95159345-A-T

Variant summary

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

The NM_005845.5(ABCC4):c.2455+1844T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.238 in 151,408 control chromosomes in the GnomAD database, including 5,247 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 0.24 (5247 hom., cov: 30)
• Consequence: ABCC4 NM_005845.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0100

Genes affected

ABCC4 (HGNC:55): (ATP binding cassette subfamily C member 4 (PEL blood group)) 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 MRP subfamily which is involved in multi-drug resistance. This family member plays a role in cellular detoxification as a pump for its substrate, organic anions. It may also function in prostaglandin-mediated cAMP signaling in ciliogenesis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Sep 2014]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.419 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
ABCC4	NM_005845.5	c.2455+1844T>C		intron_variant		ENST00000645237.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
ABCC4	ENST00000645237.2	c.2455+1844T>C		intron_variant			NM_005845.5	P1

Frequencies

GnomAD3 genomes AF: 0.238 AC: 36041 AN: 151290 Hom.: 5233 Cov.: 30

Gnomad AFR AF: 0.424

Gnomad AMI AF: 0.216

Gnomad AMR AF: 0.181

Gnomad ASJ AF: 0.171

Gnomad EAS AF: 0.124

Gnomad SAS AF: 0.189

Gnomad FIN AF: 0.151

Gnomad MID AF: 0.331

Gnomad NFE AF: 0.168

Gnomad OTH AF: 0.229

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

GnomAD4 genome AF: 0.238 AC: 36087 AN: 151408 Hom.: 5247 Cov.: 30 AF XY: 0.235 AC XY: 17346 AN XY: 73966

Gnomad4 AFR AF: 0.424

Gnomad4 AMR AF: 0.181

Gnomad4 ASJ AF: 0.171

Gnomad4 EAS AF: 0.124

Gnomad4 SAS AF: 0.190

Gnomad4 FIN AF: 0.151

Gnomad4 NFE AF: 0.168

Gnomad4 OTH AF: 0.227

Alfa AF: 0.177 Hom.: 3526

Bravo AF: 0.246

Asia WGS AF: 0.173 AC: 603 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
Cadd	Benign	2.2
Dann	Benign	0.82

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: rs1750996; hg19: chr13-95811599;