rs12704363

chr7-87546310-C-T

Variant summary

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

The NM_001348946.2(ABCB1):c.1726-286G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.311 in 152,010 control chromosomes in the GnomAD database, including 7,414 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 0.31 (7414 hom., cov: 33)
• Consequence: ABCB1 NM_001348946.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.35

Genes affected

ABCB1 (HGNC:40): (ATP binding cassette subfamily B member 1) The membrane-associated 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 MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is an ATP-dependent drug efflux pump for xenobiotic compounds with broad substrate specificity. It is responsible for decreased drug accumulation in multidrug-resistant cells and often mediates the development of resistance to anticancer drugs. This protein also functions as a transporter in the blood-brain barrier. Mutations in this gene are associated with colchicine resistance and Inflammatory bowel disease 13. Alternative splicing and the use of alternative promoters results in multiple transcript variants. [provided by RefSeq, Feb 2017]

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 (AMR) allele frequency at 95% confidence interval = 0.367 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
ABCB1	NM_001348946.2	c.1726-286G>A		intron_variant		ENST00000622132.5
ABCB1	NM_000927.5	c.1726-286G>A		intron_variant
ABCB1	NM_001348944.2	c.1726-286G>A		intron_variant
ABCB1	NM_001348945.2	c.1936-286G>A		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
ABCB1	ENST00000622132.5	c.1726-286G>A		intron_variant		1	NM_001348946.2	P1
ABCB1	ENST00000265724.8	c.1726-286G>A		intron_variant		1		P1
ABCB1	ENST00000543898.5	c.1534-286G>A		intron_variant		5
ABCB1	ENST00000482527.1	n.480-286G>A		intron_variant, non_coding_transcript_variant		4

Frequencies

GnomAD3 genomes AF: 0.311 AC: 47258 AN: 151888 Hom.: 7410 Cov.: 33

Gnomad AFR AF: 0.269

Gnomad AMI AF: 0.396

Gnomad AMR AF: 0.375

Gnomad ASJ AF: 0.390

Gnomad EAS AF: 0.299

Gnomad SAS AF: 0.211

Gnomad FIN AF: 0.299

Gnomad MID AF: 0.325

Gnomad NFE AF: 0.326

Gnomad OTH AF: 0.351

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

GnomAD4 genome AF: 0.311 AC: 47281 AN: 152010 Hom.: 7414 Cov.: 33 AF XY: 0.309 AC XY: 22991 AN XY: 74288

Gnomad4 AFR AF: 0.269

Gnomad4 AMR AF: 0.375

Gnomad4 ASJ AF: 0.390

Gnomad4 EAS AF: 0.299

Gnomad4 SAS AF: 0.212

Gnomad4 FIN AF: 0.299

Gnomad4 NFE AF: 0.326

Gnomad4 OTH AF: 0.348

Alfa AF: 0.329 Hom.: 1052

Bravo AF: 0.315

Asia WGS AF: 0.238 AC: 831 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	1.8
Dann	Benign	0.20

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: rs12704363; hg19: chr7-87175626;