rs13240966

Variant names:

• chr7-151061731-C-G
• rs13240966
• NM_003040.4:c.-63-194C>G

Your query was ambiguous. Multiple possible variants found:

• chr7-151061731-C-G
• chr7-151061731-C-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_003040.4(SLC4A2):​c.-63-194C>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.17 in 489,892 control chromosomes in the GnomAD database, including 8,292 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 0.16 (2204 hom., cov: 32)
  • Exomes 𝑓: 0.17 (6088 hom.)
• Consequence: SLC4A2 NM_003040.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -3.43

Genes affected

SLC4A2 (HGNC:11028): (solute carrier family 4 member 2) This gene encodes a member of the anion exchanger family of membrane transport proteins. The encoded protein regulates intracellular pH, biliary bicarbonate secretion, and chloride uptake. Reduced expression of this gene may be associated with primary biliary cirrhosis (PBC) in human patients, while differential expression of this gene may be associated with malignant hepatocellular carcinoma, colon and gastric cancers. [provided by RefSeq, Nov 2016]

ENSG00000288608 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.83).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.255 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SLC4A2	NM_003040.4	c.-63-194C>G		intron_variant	Intron 1 of 22	ENST00000413384.7	NP_003031.3
SLC4A2	NM_001199692.3	c.-63-194C>G		intron_variant	Intron 1 of 22		NP_001186621.1
LOC128092247	NM_001414898.1	c.-197C>G		upstream_gene_variant			NP_001401827.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SLC4A2	ENST00000413384.7	c.-63-194C>G		intron_variant	Intron 1 of 22	1	NM_003040.4	ENSP00000405600.2
ENSG00000288608	ENST00000674552.1	c.-197C>G		upstream_gene_variant				ENSP00000501917.1

Frequencies

GnomAD3 genomes AF: 0.159 AC: 24252 AN: 152088 Hom.: 2204 Cov.: 32

Gnomad AFR AF: 0.106

Gnomad AMI AF: 0.0406

Gnomad AMR AF: 0.127

Gnomad ASJ AF: 0.164

Gnomad EAS AF: 0.0161

Gnomad SAS AF: 0.268

Gnomad FIN AF: 0.135

Gnomad MID AF: 0.212

Gnomad NFE AF: 0.208

Gnomad OTH AF: 0.161

GnomAD4 exome AF: 0.174 AC: 58922 AN: 337686 Hom.: 6088 Cov.: 0 AF XY: 0.179 AC XY: 31347 AN XY: 175136

Gnomad4 AFR exome AF: 0.101

Gnomad4 AMR exome AF: 0.107

Gnomad4 ASJ exome AF: 0.153

Gnomad4 EAS exome AF: 0.0153

Gnomad4 SAS exome AF: 0.243

Gnomad4 FIN exome AF: 0.140

Gnomad4 NFE exome AF: 0.203

Gnomad4 OTH exome AF: 0.171

GnomAD4 genome AF: 0.159 AC: 24275 AN: 152206 Hom.: 2204 Cov.: 32 AF XY: 0.155 AC XY: 11519 AN XY: 74408

Gnomad4 AFR AF: 0.106

Gnomad4 AMR AF: 0.127

Gnomad4 ASJ AF: 0.164

Gnomad4 EAS AF: 0.0161

Gnomad4 SAS AF: 0.267

Gnomad4 FIN AF: 0.135

Gnomad4 NFE AF: 0.208

Gnomad4 OTH AF: 0.164

Alfa AF: 0.0649 Hom.: 80

Bravo AF: 0.151

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.83
CADD	Benign	0.057
DANN	Benign	0.42

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

Publications

LitVar

Other links and lift over

dbSNP: rs13240966; hg19: chr7-150758818;