1-11806707-C-A

Variant names:

• chr1-11806707-C-A
• NM_001286.5:c.87+358C>A

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_001286.5(CLCN6):​c.87+358C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. 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: not found (cov: 33)
  • Exomes 𝑓: 0.0 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: CLCN6 NM_001286.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0790
• Publications: 0 publications found

Genes affected

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]

CLCN6 Gene-Disease associations (from GenCC):

• neurodegeneration, childhood-onset, with hypotonia, respiratory insufficiency, and brain imaging abnormalities

  Inheritance: AD Classification: STRONG, LIMITED Submitted by: Labcorp Genetics (formerly Invitae), G2P, Ambry Genetics

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.76).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CLCN6	NM_001286.5	c.87+358C>A		intron_variant	Intron 1 of 22	ENST00000346436.11	NP_001277.2
CLCN6	NM_001256959.2	c.87+358C>A		intron_variant	Intron 1 of 21		NP_001243888.2
CLCN6	NR_046428.2	n.159+358C>A		intron_variant	Intron 1 of 22

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CLCN6	ENST00000346436.11	c.87+358C>A		intron_variant	Intron 1 of 22	1	NM_001286.5	ENSP00000234488.9

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0 AN: 201632 Hom.: 0 Cov.: 0 AF XY: 0.00 AC XY: 0 AN XY: 103926

African (AFR) AF: 0.00 AC: 0 AN: 5642

American (AMR) AF: 0.00 AC: 0 AN: 5646

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 7466

East Asian (EAS) AF: 0.00 AC: 0 AN: 14344

South Asian (SAS) AF: 0.00 AC: 0 AN: 12524

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 13560

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 1022

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 128092

Other (OTH) AF: 0.00 AC: 0 AN: 13336

GnomAD4 genome Cov.: 33

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.76
CADD	Benign	8.3
DANN	Benign	0.64
PhyloP100		0.079
PromoterAI		0.021	Neutral

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

hg19: chr1-11866764;