rs871540

chr4-154487878-G-Achr4-154487878-G-Cchr4-154487878-G-T

Variant summary

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

The NM_001358235.2(DCHS2):c.2052+1426C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.697 in 152,150 control chromosomes in the GnomAD database, including 38,032 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 0.70 (38032 hom., cov: 33)
• Consequence: DCHS2 NM_001358235.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.264

Genes affected

DCHS2 (HGNC:23111): (dachsous cadherin-related 2) This gene encodes a large protein that contains many cadherin domains and likely functions in cell adhesion. Genome-wide association studies suggest that this gene may be important in Alzheimer's disease, compressive strength index, and appendicular lean mass. [provided by RefSeq, May 2017]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.966 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
DCHS2	NM_001358235.2	c.2052+1426C>T		intron_variant		ENST00000357232.10
DCHS2	NM_001142552.2	c.2052+1426C>T		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
DCHS2	ENST00000357232.10	c.2052+1426C>T		intron_variant		1	NM_001358235.2	P1
DCHS2	ENST00000339452.2	c.2052+1426C>T		intron_variant		1
DCHS2	ENST00000456341.2	n.2032-1358C>T		intron_variant, non_coding_transcript_variant		1

Frequencies

GnomAD3 genomes AF: 0.697 AC: 105935 AN: 152032 Hom.: 38016 Cov.: 33

Gnomad AFR AF: 0.526

Gnomad AMI AF: 0.791

Gnomad AMR AF: 0.784

Gnomad ASJ AF: 0.766

Gnomad EAS AF: 0.989

Gnomad SAS AF: 0.785

Gnomad FIN AF: 0.832

Gnomad MID AF: 0.703

Gnomad NFE AF: 0.727

Gnomad OTH AF: 0.682

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

GnomAD4 genome AF: 0.697 AC: 105998 AN: 152150 Hom.: 38032 Cov.: 33 AF XY: 0.706 AC XY: 52547 AN XY: 74396

Gnomad4 AFR AF: 0.526

Gnomad4 AMR AF: 0.784

Gnomad4 ASJ AF: 0.766

Gnomad4 EAS AF: 0.989

Gnomad4 SAS AF: 0.786

Gnomad4 FIN AF: 0.832

Gnomad4 NFE AF: 0.727

Gnomad4 OTH AF: 0.681

Alfa AF: 0.723 Hom.: 19542

Bravo AF: 0.684

Asia WGS AF: 0.858 AC: 2984 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
Cadd	Benign	1.7
Dann	Benign	0.49

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs871540; hg19: chr4-155409030;