1-205915146-T-C

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_Strong BP6_Moderate BA1

The ENST00000340781.8(SLC26A9):c.2410A>G(p.Arg804Gly) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.103 in 1,613,058 control chromosomes in the GnomAD database, including 13,016 homozygotes. In-silico tool predicts a benign outcome for this variant. 13/17 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency:
  • Genomes: 𝑓 0.18 (4034 hom., cov: 32)
  • Exomes 𝑓: 0.095 (8982 hom.)
• Consequence: SLC26A9 ENST00000340781.8 missense
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: 0.509

Genes affected

SLC26A9 (HGNC:14469): (solute carrier family 26 member 9) This gene is one member of a family of sulfate/anion transporter genes. Family members are well conserved in their genomic (number and size of exons) and protein (aa length among species) structures yet have markedly different tissue expression patterns. The product of this gene is a highly selective chloride ion channel regulated by WNK kinases. Alternative splicing results in multiple transcript variants encoding differing isoforms.[provided by RefSeq, Dec 2008]

ACMG classification

Verdict is Benign. Variant got -14 ACMG points.

• BP4: Computational evidence support a benign effect (MetaRNN=4.041791E-4).
• BP6: Variant 1-205915146-T-C is Benign according to our data. Variant chr1-205915146-T-C is described in ClinVar as [Benign]. Clinvar id is 403451.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.403 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
SLC26A9	NM_052934.4	c.*211A>G		3_prime_UTR_variant	21/21	ENST00000367135.8
SLC26A9	NM_134325.3	c.2410A>G	p.Arg804Gly	missense_variant	22/22
SLC26A9	XM_011509121.3	c.*211A>G		3_prime_UTR_variant	20/20
SLC26A9	XM_011509122.3	c.*211A>G		3_prime_UTR_variant	18/18

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
SLC26A9	ENST00000340781.8	c.2410A>G	p.Arg804Gly	missense_variant	21/21	1
SLC26A9	ENST00000367135.8	c.*211A>G		3_prime_UTR_variant	21/21	1	NM_052934.4	P1
SLC26A9	ENST00000367134.2	c.2410A>G	p.Arg804Gly	missense_variant	22/22	5
SLC26A9	ENST00000491127.5	n.1971A>G		non_coding_transcript_exon_variant	13/13	2

Frequencies

GnomAD3 genomes AF: 0.179 AC: 27221 AN: 151786 Hom.: 4023 Cov.: 32

Gnomad AFR AF: 0.408

Gnomad AMI AF: 0.204

Gnomad AMR AF: 0.121

Gnomad ASJ AF: 0.113

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.0193

Gnomad FIN AF: 0.103

Gnomad MID AF: 0.108

Gnomad NFE AF: 0.0942

Gnomad OTH AF: 0.173

GnomAD3 exomes AF: 0.0995 AC: 24903 AN: 250402 Hom.: 2301 AF XY: 0.0917 AC XY: 12410 AN XY: 135284

Gnomad AFR exome AF: 0.417

Gnomad AMR exome AF: 0.0709

Gnomad ASJ exome AF: 0.111

Gnomad EAS exome AF: 0.00

Gnomad SAS exome AF: 0.0215

Gnomad FIN exome AF: 0.103

Gnomad NFE exome AF: 0.0983

Gnomad OTH exome AF: 0.0981

GnomAD4 exome AF: 0.0948 AC: 138455 AN: 1461154 Hom.: 8982 Cov.: 32 AF XY: 0.0919 AC XY: 66778 AN XY: 726772

Gnomad4 AFR exome AF: 0.427

Gnomad4 AMR exome AF: 0.0751

Gnomad4 ASJ exome AF: 0.111

Gnomad4 EAS exome AF: 0.0000756

Gnomad4 SAS exome AF: 0.0209

Gnomad4 FIN exome AF: 0.101

Gnomad4 NFE exome AF: 0.0934

Gnomad4 OTH exome AF: 0.101

GnomAD4 genome AF: 0.180 AC: 27272 AN: 151904 Hom.: 4034 Cov.: 32 AF XY: 0.173 AC XY: 12881 AN XY: 74242

Gnomad4 AFR AF: 0.408

Gnomad4 AMR AF: 0.121

Gnomad4 ASJ AF: 0.113

Gnomad4 EAS AF: 0.00

Gnomad4 SAS AF: 0.0191

Gnomad4 FIN AF: 0.103

Gnomad4 NFE AF: 0.0942

Gnomad4 OTH AF: 0.172

Alfa AF: 0.106 Hom.: 3139

Bravo AF: 0.193

TwinsUK AF: 0.0903 AC: 335

ALSPAC AF: 0.0856 AC: 330

ESP6500AA AF: 0.400 AC: 1764

ESP6500EA AF: 0.0964 AC: 829

ExAC AF: 0.105 AC: 12713

Asia WGS AF: 0.0400 AC: 137 AN: 3478

EpiCase AF: 0.104

EpiControl AF: 0.106

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not specified Benign:1

Benign, criteria provided, single submitter

clinical testing

Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Mar 29, 2016

Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: Frequency -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_addAF	Benign	-0.52	T
BayesDel_noAF	Benign	-0.38
Cadd	Benign	7.9
Dann	Benign	0.90
Eigen	Benign	-1.1
Eigen_PC	Benign	-1.2
FATHMM_MKL	Benign	0.15	N
MetaRNN	Benign	0.00040	T;T
MetaSVM	Benign	-0.98	T
MutationTaster	Benign	1.0	P;P;P
PrimateAI	Benign	0.26	T
PROVEAN	Benign	-0.040	N;N
REVEL	Benign	0.14
Sift	Pathogenic	0.0	D;D
Sift4G	Uncertain	0.055	T;T
Vest4		0.049
MPC		0.18
ClinPred		0.015	T
GERP RS		0.71
gMVP		0.23

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.070		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: rs6669481; hg19: chr1-205884274; COSMIC: COSV61604404;