ENST00000377890.6:c.299-491A>G

Variant names:

• chr11-62880528-A-G
• rs7126772
• ENST00000377890.6:c.299-491A>G

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BS1 BS2

The ENST00000377890.6(SLC3A2):​c.299-491A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0106 in 153,078 control chromosomes in the GnomAD database, including 20 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 0.011 (20 hom., cov: 32)
  • Exomes 𝑓: 0.0012 (0 hom.)
• Consequence: SLC3A2 ENST00000377890.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.36
• Publications: 0 publications found

Genes affected

SLC3A2 (HGNC:11026): (solute carrier family 3 member 2) This gene is a member of the solute carrier family and encodes a cell surface, transmembrane protein. The protein exists as the heavy chain of a heterodimer, covalently bound through di-sulfide bonds to one of several possible light chains. The encoded transporter plays a role in regulation of intracellular calcium levels and transports L-type amino acids. Alternatively spliced transcript variants, encoding different isoforms, have been characterized. [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=-0.85).
• BS1: Variant frequency is greater than expected in population afr. GnomAd4 allele frequency = 0.0106 (1617/152240) while in subpopulation AFR AF = 0.0368 (1527/41526). AF 95% confidence interval is 0.0352. There are 20 homozygotes in GnomAd4. There are 735 alleles in the male GnomAd4 subpopulation. Median coverage is 32. This position passed quality control check.
• BS2: High AC in GnomAd4 at 1617 AD gene.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SLC3A2	NM_001012662.3	c.302-491A>G		intron_variant	Intron 3 of 11		NP_001012680.1
SLC3A2	NM_002394.6	c.299-491A>G		intron_variant	Intron 3 of 11		NP_002385.3
SLC3A2	NM_001012664.3	c.113-491A>G		intron_variant	Intron 1 of 9		NP_001012682.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SLC3A2	ENST00000377890.6	c.299-491A>G		intron_variant	Intron 3 of 11	1		ENSP00000367122.2
SLC3A2	ENST00000377889.6	c.113-491A>G		intron_variant	Intron 1 of 9	1		ENSP00000367121.2
SLC3A2	ENST00000544377.2	c.-78A>G		5_prime_UTR_variant	Exon 1 of 10	4		ENSP00000442135.2

Frequencies

GnomAD3 genomes AF: 0.0106 AC: 1618 AN: 152122 Hom.: 20 Cov.: 32

Gnomad AFR AF: 0.0369

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.00387

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.000207

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.00633

Gnomad NFE AF: 0.000176

Gnomad OTH AF: 0.00766

GnomAD4 exome AF: 0.00119 AC: 1 AN: 838 Hom.: 0 Cov.: 0 AF XY: 0.00 AC XY: 0 AN XY: 512

African (AFR) AF: 0.00 AC: 0 AN: 24

American (AMR) AF: 0.0333 AC: 1 AN: 30

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 30

East Asian (EAS) AF: 0.00 AC: 0 AN: 16

South Asian (SAS) AF: 0.00 AC: 0 AN: 190

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 20

Middle Eastern (MID) AC: 0 AN: 0

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 478

Other (OTH) AF: 0.00 AC: 0 AN: 50

GnomAD4 genome AF: 0.0106 AC: 1617 AN: 152240 Hom.: 20 Cov.: 32 AF XY: 0.00987 AC XY: 735 AN XY: 74440

African (AFR) AF: 0.0368 AC: 1527 AN: 41526

American (AMR) AF: 0.00386 AC: 59 AN: 15282

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 3472

East Asian (EAS) AF: 0.00 AC: 0 AN: 5184

South Asian (SAS) AF: 0.000207 AC: 1 AN: 4824

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 10612

Middle Eastern (MID) AF: 0.00680 AC: 2 AN: 294

European-Non Finnish (NFE) AF: 0.000176 AC: 12 AN: 68022

Other (OTH) AF: 0.00758 AC: 16 AN: 2112

Alfa AF: 0.00523 Hom.: 3

Bravo AF: 0.0125

Asia WGS AF: 0.00231 AC: 8 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
CADD	Benign	0.25
DANN	Benign	0.37
PhyloP100		-1.4
PromoterAI		0.016	Neutral
Mutation Taster		=100/0	polymorphism

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: rs7126772; hg19: chr11-62648000;