1-11846856-C-G

Variant names:

• chr1-11846856-C-G
• rs198368
• NM_006172.4:c.450+257G>C

Variant summary

Our verdict is Benign. The variant received -14 ACMG points: 0P and 14B. BP4_Strong BP6_Moderate BA1

The NM_006172.4(NPPA):​c.450+257G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.136 in 151,000 control chromosomes in the GnomAD database, including 2,137 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency: Genomes: 𝑓 0.14 (2137 hom., cov: 28)
• Consequence: NPPA NM_006172.4 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -2.31
• Publications: 6 publications found

Genes affected

NPPA (HGNC:7939): (natriuretic peptide A) The protein encoded by this gene belongs to the natriuretic peptide family. Natriuretic peptides are implicated in the control of extracellular fluid volume and electrolyte homeostasis. This protein is synthesized as a large precursor (containing a signal peptide), which is processed to release a peptide from the N-terminus with similarity to vasoactive peptide, cardiodilatin, and another peptide from the C-terminus with natriuretic-diuretic activity. Mutations in this gene have been associated with atrial fibrillation familial type 6. This gene is located adjacent to another member of the natriuretic family of peptides on chromosome 1. [provided by RefSeq, Oct 2015]

CLCN6 (HGNC:2024): (chloride voltage-gated channel 6) This gene encodes a member of the voltage-dependent chloride channel protein family. Members of this family can function as either chloride channels or antiporters. This protein is primarily localized to late endosomes and functions as a chloride/proton antiporter. Alternate splicing results in both coding and non-coding variants. Additional alternately spliced variants have been described but their full-length structure is unknown. [provided by RefSeq, Mar 2012]

NPPA-AS1 (HGNC:37635): (NPPA antisense RNA 1)

ACMG classification

Our verdict: Benign. The variant received -14 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.07).
• BP6: Variant 1-11846856-C-G is Benign according to our data. Variant chr1-11846856-C-G is described in ClinVar as Benign. ClinVar VariationId is 1182455.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.285 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_006172.4. 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
	NPPA	NM_006172.4	MANE Select	c.450+257G>C		intron	N/A	NP_006163.1	P01160
	NPPA-AS1	NR_037806.1		n.1480-578C>G		intron	N/A

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	NPPA	ENST00000376480.7	TSL:1 MANE Select	c.450+257G>C		intron	N/A	ENSP00000365663.3	P01160
	CLCN6	ENST00000446542.5	TSL:1	n.782-578C>G		intron	N/A
	NPPA	ENST00000376476.1	TSL:3	c.300+257G>C		intron	N/A	ENSP00000365659.1	B0ZBE8

Frequencies

GnomAD3 genomes AF: 0.136 AC: 20471 AN: 150884 Hom.: 2136 Cov.: 28

Gnomad AFR AF: 0.290

Gnomad AMI AF: 0.0991

Gnomad AMR AF: 0.0883

Gnomad ASJ AF: 0.0514

Gnomad EAS AF: 0.00659

Gnomad SAS AF: 0.0943

Gnomad FIN AF: 0.0383

Gnomad MID AF: 0.152

Gnomad NFE AF: 0.0862

Gnomad OTH AF: 0.136

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

GnomAD4 genome AF: 0.136 AC: 20486 AN: 151000 Hom.: 2137 Cov.: 28 AF XY: 0.133 AC XY: 9795 AN XY: 73786

African (AFR) AF: 0.289 AC: 11814 AN: 40822

American (AMR) AF: 0.0882 AC: 1342 AN: 15218

Ashkenazi Jewish (ASJ) AF: 0.0514 AC: 178 AN: 3460

East Asian (EAS) AF: 0.00660 AC: 34 AN: 5148

South Asian (SAS) AF: 0.0942 AC: 452 AN: 4798

European-Finnish (FIN) AF: 0.0383 AC: 399 AN: 10420

Middle Eastern (MID) AF: 0.160 AC: 47 AN: 294

European-Non Finnish (NFE) AF: 0.0862 AC: 5847 AN: 67832

Other (OTH) AF: 0.135 AC: 283 AN: 2100

Alfa AF: 0.0330 Hom.: 23

Bravo AF: 0.148

Asia WGS AF: 0.0580 AC: 201 AN: 3478

ClinVar

ClinVar submissions

Significance: Benign

Revision: criteria provided, single submitter

Pathogenic	VUS	Benign	Condition
-	-	1	not provided (1)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.1
CADD	Benign	0.11
DANN	Benign	0.28
PhyloP100		-2.3
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: rs198368; hg19: chr1-11906913;