6-160350778-C-T

Variant names:

• chr6-160350778-C-T
• rs509707
• NM_021977.4:c.429+1930C>T

Variant summary

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

The NM_021977.4(SLC22A3):​c.429+1930C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.502 in 151,932 control chromosomes in the GnomAD database, including 19,443 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 0.50 (19443 hom., cov: 32)
• Consequence: SLC22A3 NM_021977.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.486
• Publications: 14 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=-0.91).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.584 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_021977.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SLC22A3	NM_021977.4	MANE Select	c.429+1930C>T		intron	N/A	NP_068812.1	O75751

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SLC22A3	ENST00000275300.3	TSL:1 MANE Select	c.429+1930C>T		intron	N/A	ENSP00000275300.2	O75751
	SLC22A3	ENST00000855214.1		c.429+1930C>T		intron	N/A	ENSP00000525273.1
	SLC22A3	ENST00000855213.1		c.429+1930C>T		intron	N/A	ENSP00000525272.1

Frequencies

GnomAD3 genomes AF: 0.502 AC: 76144 AN: 151808 Hom.: 19407 Cov.: 32

Gnomad AFR AF: 0.590

Gnomad AMI AF: 0.384

Gnomad AMR AF: 0.431

Gnomad ASJ AF: 0.552

Gnomad EAS AF: 0.300

Gnomad SAS AF: 0.363

Gnomad FIN AF: 0.498

Gnomad MID AF: 0.509

Gnomad NFE AF: 0.489

Gnomad OTH AF: 0.493

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

GnomAD4 genome AF: 0.502 AC: 76235 AN: 151932 Hom.: 19443 Cov.: 32 AF XY: 0.499 AC XY: 37044 AN XY: 74242

African (AFR) AF: 0.590 AC: 24467 AN: 41440

American (AMR) AF: 0.429 AC: 6554 AN: 15262

Ashkenazi Jewish (ASJ) AF: 0.552 AC: 1917 AN: 3472

East Asian (EAS) AF: 0.300 AC: 1552 AN: 5166

South Asian (SAS) AF: 0.365 AC: 1756 AN: 4816

European-Finnish (FIN) AF: 0.498 AC: 5250 AN: 10534

Middle Eastern (MID) AF: 0.507 AC: 149 AN: 294

European-Non Finnish (NFE) AF: 0.489 AC: 33201 AN: 67924

Other (OTH) AF: 0.492 AC: 1040 AN: 2114

Alfa AF: 0.492 Hom.: 7975

Bravo AF: 0.505

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	2.2
DANN	Benign	0.51
PhyloP100		-0.49
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: rs509707; hg19: chr6-160771810;