rs2063345

Variant names:

• chr6-160439122-A-G
• rs2063345
• NM_021977.4:c.1288+1911A>G

Variant summary

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

The NM_021977.4(SLC22A3):​c.1288+1911A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.247 in 151,894 control chromosomes in the GnomAD database, including 5,107 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 0.25 (5107 hom., cov: 31)
• Consequence: SLC22A3 NM_021977.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.233
• Publications: 12 publications found

Genes affected

SLC22A3 (HGNC:10967): (solute carrier family 22 member 3) Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. [provided by RefSeq, Jul 2008]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.403 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SLC22A3	NM_021977.4	c.1288+1911A>G		intron_variant	Intron 7 of 10	ENST00000275300.3	NP_068812.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SLC22A3	ENST00000275300.3	c.1288+1911A>G		intron_variant	Intron 7 of 10	1	NM_021977.4	ENSP00000275300.2

Frequencies

GnomAD3 genomes AF: 0.247 AC: 37520 AN: 151776 Hom.: 5105 Cov.: 31

Gnomad AFR AF: 0.141

Gnomad AMI AF: 0.197

Gnomad AMR AF: 0.199

Gnomad ASJ AF: 0.359

Gnomad EAS AF: 0.417

Gnomad SAS AF: 0.393

Gnomad FIN AF: 0.294

Gnomad MID AF: 0.285

Gnomad NFE AF: 0.286

Gnomad OTH AF: 0.276

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

GnomAD4 genome AF: 0.247 AC: 37545 AN: 151894 Hom.: 5107 Cov.: 31 AF XY: 0.250 AC XY: 18594 AN XY: 74228

African (AFR) AF: 0.141 AC: 5842 AN: 41434

American (AMR) AF: 0.199 AC: 3036 AN: 15250

Ashkenazi Jewish (ASJ) AF: 0.359 AC: 1240 AN: 3458

East Asian (EAS) AF: 0.418 AC: 2146 AN: 5136

South Asian (SAS) AF: 0.393 AC: 1899 AN: 4826

European-Finnish (FIN) AF: 0.294 AC: 3097 AN: 10522

Middle Eastern (MID) AF: 0.286 AC: 84 AN: 294

European-Non Finnish (NFE) AF: 0.286 AC: 19439 AN: 67954

Other (OTH) AF: 0.276 AC: 583 AN: 2110

Alfa AF: 0.279 Hom.: 12141

Bravo AF: 0.236

Asia WGS AF: 0.387 AC: 1343 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	0.096
DANN	Benign	0.31
PhyloP100		-0.23
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: rs2063345; hg19: chr6-160860154;