rs4275659

Variant names:

• chr12-122963381-T-C
• rs4275659
• NM_019625.4:c.-88+2906A>G

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_019625.4(ABCB9):​c.-88+2906A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.546 in 152,062 control chromosomes in the GnomAD database, including 27,134 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 0.55 (27134 hom., cov: 31)
• Consequence: ABCB9 NM_019625.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.27
• Publications: 59 publications found

Genes affected

ABCB9 (HGNC:50): (ATP binding cassette subfamily B member 9) 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 as well as antigen presentation. This family member functions in the translocation of peptides from the cytosol into the lysosomal lumen. Alternative splicing of this gene results in distinct isoforms which are likely to have different substrate specificities. [provided by RefSeq, Jul 2011]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.705 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ABCB9	NM_019625.4	c.-88+2906A>G		intron_variant	Intron 1 of 11	ENST00000280560.13	NP_062571.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ABCB9	ENST00000280560.13	c.-88+2906A>G		intron_variant	Intron 1 of 11	1	NM_019625.4	ENSP00000280560.8

Frequencies

GnomAD3 genomes AF: 0.546 AC: 82964 AN: 151944 Hom.: 27140 Cov.: 31

Gnomad AFR AF: 0.162

Gnomad AMI AF: 0.747

Gnomad AMR AF: 0.639

Gnomad ASJ AF: 0.626

Gnomad EAS AF: 0.694

Gnomad SAS AF: 0.582

Gnomad FIN AF: 0.715

Gnomad MID AF: 0.563

Gnomad NFE AF: 0.711

Gnomad OTH AF: 0.580

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

GnomAD4 genome AF: 0.546 AC: 82956 AN: 152062 Hom.: 27134 Cov.: 31 AF XY: 0.549 AC XY: 40844 AN XY: 74330

African (AFR) AF: 0.162 AC: 6713 AN: 41472

American (AMR) AF: 0.638 AC: 9748 AN: 15284

Ashkenazi Jewish (ASJ) AF: 0.626 AC: 2169 AN: 3466

East Asian (EAS) AF: 0.694 AC: 3586 AN: 5170

South Asian (SAS) AF: 0.584 AC: 2811 AN: 4816

European-Finnish (FIN) AF: 0.715 AC: 7567 AN: 10584

Middle Eastern (MID) AF: 0.568 AC: 167 AN: 294

European-Non Finnish (NFE) AF: 0.711 AC: 48296 AN: 67958

Other (OTH) AF: 0.578 AC: 1218 AN: 2106

Alfa AF: 0.646 Hom.: 83418

Bravo AF: 0.519

Asia WGS AF: 0.572 AC: 1991 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	3.6
DANN	Benign	0.82
PhyloP100		-1.3
Mutation Taster		=100/0	polymorphism (auto)

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: rs4275659; hg19: chr12-123447928;