11-75141055-T-G

Variant names:

• chr11-75141055-T-G
• rs2712800
• ENST00000531713.5:c.-50-21600T>G

Variant summary

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

The ENST00000531713.5(SLCO2B1):​c.-50-21600T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.506 in 152,104 control chromosomes in the GnomAD database, including 20,701 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 0.51 (20701 hom., cov: 32)
• Consequence: SLCO2B1 ENST00000531713.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.287
• Publications: 5 publications found

Genes affected

SLCO2B1 (HGNC:10962): (solute carrier organic anion transporter family member 2B1) This locus encodes a member of the organic anion-transporting polypeptide family of membrane proteins. The protein encoded by this locus may function in regulation of placental uptake of sulfated steroids. Alternatively spliced transcript variants have been described. [provided by RefSeq, Nov 2010]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.83).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.609 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000531713.5. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SLCO2B1	ENST00000531713.5	TSL:3	c.-50-21600T>G		intron	N/A	ENSP00000432889.1
	SLCO2B1	ENST00000526660.5	TSL:3	n.294-31324T>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.506 AC: 76926 AN: 151986 Hom.: 20697 Cov.: 32

Gnomad AFR AF: 0.340

Gnomad AMI AF: 0.697

Gnomad AMR AF: 0.487

Gnomad ASJ AF: 0.514

Gnomad EAS AF: 0.240

Gnomad SAS AF: 0.521

Gnomad FIN AF: 0.587

Gnomad MID AF: 0.554

Gnomad NFE AF: 0.614

Gnomad OTH AF: 0.554

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

GnomAD4 genome AF: 0.506 AC: 76966 AN: 152104 Hom.: 20701 Cov.: 32 AF XY: 0.505 AC XY: 37539 AN XY: 74360

African (AFR) AF: 0.340 AC: 14116 AN: 41498

American (AMR) AF: 0.487 AC: 7439 AN: 15290

Ashkenazi Jewish (ASJ) AF: 0.514 AC: 1785 AN: 3470

East Asian (EAS) AF: 0.239 AC: 1236 AN: 5168

South Asian (SAS) AF: 0.521 AC: 2502 AN: 4806

European-Finnish (FIN) AF: 0.587 AC: 6213 AN: 10578

Middle Eastern (MID) AF: 0.541 AC: 159 AN: 294

European-Non Finnish (NFE) AF: 0.614 AC: 41720 AN: 67976

Other (OTH) AF: 0.550 AC: 1162 AN: 2114

Alfa AF: 0.568 Hom.: 13247

Bravo AF: 0.488

Asia WGS AF: 0.370 AC: 1291 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.83
CADD	Benign	1.9
DANN	Benign	0.69
PhyloP100		-0.29

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs2712800; hg19: chr11-74852100;