chr13-71844162-T-C

Position:

• chr13-71844162-T-C

Variant summary

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

The NM_080759.6(DACH1):​c.848+21760A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0637 in 152,280 control chromosomes in the GnomAD database, including 340 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 0.064 (340 hom., cov: 32)
• Consequence: DACH1 NM_080759.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.934

Genes affected

DACH1 (HGNC:2663): (dachshund family transcription factor 1) This gene encodes a chromatin-associated protein that associates with other DNA-binding transcription factors to regulate gene expression and cell fate determination during development. The protein contains a Ski domain that is highly conserved from Drosophila to human. Expression of this gene is lost in some forms of metastatic cancer, and is correlated with poor prognosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]

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 = 0.0981 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
DACH1	NM_080759.6	c.848+21760A>G		intron_variant		ENST00000613252.5	NP_542937.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
DACH1	ENST00000613252.5	c.848+21760A>G		intron_variant		1	NM_080759.6	ENSP00000482245	P2
DACH1	ENST00000619232.2	c.848+21760A>G		intron_variant		5		ENSP00000482797	A2
DACH1	ENST00000706274.1	c.391+21760A>G		intron_variant				ENSP00000516320

Frequencies

GnomAD3 genomes AF: 0.0636 AC: 9685 AN: 152162 Hom.: 338 Cov.: 32

Gnomad AFR AF: 0.0842

Gnomad AMI AF: 0.0484

Gnomad AMR AF: 0.0520

Gnomad ASJ AF: 0.0680

Gnomad EAS AF: 0.106

Gnomad SAS AF: 0.0676

Gnomad FIN AF: 0.0380

Gnomad MID AF: 0.0380

Gnomad NFE AF: 0.0543

Gnomad OTH AF: 0.0649

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

GnomAD4 genome AF: 0.0637 AC: 9700 AN: 152280 Hom.: 340 Cov.: 32 AF XY: 0.0638 AC XY: 4751 AN XY: 74460

Gnomad4 AFR AF: 0.0843

Gnomad4 AMR AF: 0.0520

Gnomad4 ASJ AF: 0.0680

Gnomad4 EAS AF: 0.105

Gnomad4 SAS AF: 0.0679

Gnomad4 FIN AF: 0.0380

Gnomad4 NFE AF: 0.0544

Gnomad4 OTH AF: 0.0662

Alfa AF: 0.0575 Hom.: 106

Bravo AF: 0.0661

Asia WGS AF: 0.0880 AC: 305 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	0.11
DANN	Benign	0.70

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: rs10492537; hg19: chr13-72418294;