rs3785368

chr16-23309459-G-A

Variant summary

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

The NM_000336.3(SCNN1B):c.-9+7022G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.178 in 152,022 control chromosomes in the GnomAD database, including 2,580 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 0.18 (2580 hom., cov: 32)
• Consequence: SCNN1B NM_000336.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.252

Genes affected

SCNN1B (HGNC:10600): (sodium channel epithelial 1 subunit beta) Nonvoltage-gated, amiloride-sensitive, sodium channels control fluid and electrolyte transport across epithelia in many organs. These channels are heteromeric complexes consisting of 3 subunits: alpha, beta, and gamma. This gene encodes the beta subunit, and mutations in this gene have been associated with pseudohypoaldosteronism type 1 (PHA1), and Liddle syndrome. [provided by RefSeq, Apr 2009]

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 (EAS) allele frequency at 95% confidence interval = 0.263 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
SCNN1B	NM_000336.3	c.-9+7022G>A		intron_variant		ENST00000343070.7
SCNN1B	NM_001410900.1	c.-9+7022G>A		intron_variant
SCNN1B	XM_011545913.3	c.-1+7022G>A		intron_variant
SCNN1B	XM_017023525.2	c.49+25655G>A		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
SCNN1B	ENST00000343070.7	c.-9+7022G>A		intron_variant		1	NM_000336.3	P1
SCNN1B	ENST00000307331.9	c.102+5358G>A		intron_variant		5
SCNN1B	ENST00000569789.1	n.178+25655G>A		intron_variant, non_coding_transcript_variant		4

Frequencies

GnomAD3 genomes AF: 0.179 AC: 27117 AN: 151902 Hom.: 2574 Cov.: 32

Gnomad AFR AF: 0.120

Gnomad AMI AF: 0.0892

Gnomad AMR AF: 0.186

Gnomad ASJ AF: 0.204

Gnomad EAS AF: 0.275

Gnomad SAS AF: 0.253

Gnomad FIN AF: 0.210

Gnomad MID AF: 0.291

Gnomad NFE AF: 0.193

Gnomad OTH AF: 0.223

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

GnomAD4 genome AF: 0.178 AC: 27128 AN: 152022 Hom.: 2580 Cov.: 32 AF XY: 0.181 AC XY: 13472 AN XY: 74286

Gnomad4 AFR AF: 0.120

Gnomad4 AMR AF: 0.186

Gnomad4 ASJ AF: 0.204

Gnomad4 EAS AF: 0.275

Gnomad4 SAS AF: 0.254

Gnomad4 FIN AF: 0.210

Gnomad4 NFE AF: 0.193

Gnomad4 OTH AF: 0.226

Alfa AF: 0.181 Hom.: 389

Bravo AF: 0.174

Asia WGS AF: 0.283 AC: 982 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.83
Cadd	Benign	0.65
Dann	Benign	0.57

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: rs3785368; hg19: chr16-23320780;