Variant chr10-86666837-G-T details in Genebe, Genetics Data Aggregator

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_StrongBP6_ModerateBS1BS2

The NM_001368064.1(LDB3):c.-35G>T variant causes a 5 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000694 in 469,870 control chromosomes in the GnomAD database, including 2 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★).

Frequency

Genomes: 𝑓 0.0018 ( 2 hom., cov: 33)

Exomes 𝑓: 0.00017 ( 0 hom. )

Consequence

LDB3
NM_001368064.1 5_prime_UTR

Scores

Clinical Significance

Likely benign criteria provided, single submitter B:1

Conservation

PhyloP100: 0.143

Variant links:

Genes affected

LDB3 (HGNC:15710): (LIM domain binding 3) This gene encodes a PDZ domain-containing protein. PDZ motifs are modular protein-protein interaction domains consisting of 80-120 amino acid residues. PDZ domain-containing proteins interact with each other in cytoskeletal assembly or with other proteins involved in targeting and clustering of membrane proteins. The protein encoded by this gene interacts with alpha-actinin-2 through its N-terminal PDZ domain and with protein kinase C via its C-terminal LIM domains. The LIM domain is a cysteine-rich motif defined by 50-60 amino acids containing two zinc-binding modules. This protein also interacts with all three members of the myozenin family. Mutations in this gene have been associated with myofibrillar myopathy and dilated cardiomyopathy. Alternatively spliced transcript variants encoding different isoforms have been identified; all isoforms have N-terminal PDZ domains while only longer isoforms (1, 2 and 5) have C-terminal LIM domains. [provided by RefSeq, Jan 2010]

LDB3 links:

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -14 ACMG points.

BP4

Computational evidence support a benign effect (MetaRNN=0.0030962229).

BP6

Variant 10-86666837-G-T is Benign according to our data. Variant chr10-86666837-G-T is described in ClinVar as [Likely_benign]. Clinvar id is 2640653.Status of the report is criteria_provided_single_submitter, 1 stars.

BS1

Variant frequency is greater than expected in population afr. gnomad4 allele frequency = 0.0018 (273/151374) while in subpopulation AFR AF= 0.00642 (265/41284). AF 95% confidence interval is 0.00578. There are 2 homozygotes in gnomad4. There are 132 alleles in male gnomad4 subpopulation. Median coverage is 33. This position pass quality control queck.

BS2

High AC in GnomAd4 at 273 AD gene.

Transcripts

RefSeq

Gene	Transcript	HGVSc	Effect	#exon/exons
LDB3	NM_001368063.1 linkuse as main transcript	c.-35G>T	5_prime_UTR_variant	1/8
LDB3	NM_001368064.1 linkuse as main transcript	c.-35G>T	5_prime_UTR_variant	1/13
LDB3	NM_001368068.1 linkuse as main transcript	c.-35G>T	5_prime_UTR_variant	1/9

Ensembl

Gene	Transcript	HGVSc	Effect	#exon/exons	Appris
LDB3	ENST00000688001.1 linkuse as main transcript	c.-35G>T	5_prime_UTR_variant	1/13	A2
LDB3	ENST00000688785.1 linkuse as main transcript	c.-35G>T	5_prime_UTR_variant	1/8
LDB3	ENST00000691462.1 linkuse as main transcript	c.-35G>T	5_prime_UTR_variant	1/8
LDB3	ENST00000687856.1 linkuse as main transcript	c.-35G>T	5_prime_UTR_variant, NMD_transcript_variant	1/6

Frequencies

GnomAD3 genomes

AF:

0.00180

AC:

273

AN:

151252

Hom.:

Cov.:

show subpopulations

Gnomad AFR

AF:

0.00644

Gnomad AMI

AF:

0.00

Gnomad AMR

AF:

0.000397

Gnomad ASJ

AF:

0.00

Gnomad EAS

AF:

0.00

Gnomad SAS

AF:

0.00

Gnomad FIN

AF:

0.00

Gnomad MID

AF:

0.00

Gnomad NFE

AF:

0.00

Gnomad OTH

AF:

0.000963

GnomAD3 exomes

AF:

0.000305

AC:

AN:

147742

Hom.:

AF XY:

0.000239

AC XY:

AN XY:

79616

show subpopulations

Gnomad AFR exome

AF:

0.00586

Gnomad AMR exome

AF:

0.0000816

Gnomad ASJ exome

AF:

0.00

Gnomad EAS exome

AF:

0.00

Gnomad SAS exome

AF:

0.00

Gnomad FIN exome

AF:

0.00

Gnomad NFE exome

AF:

0.0000365

Gnomad OTH exome

AF:

0.000233

GnomAD4 exome

AF:

0.000166

AC:

AN:

318496

Hom.:

Cov.:

AF XY:

0.000117

AC XY:

AN XY:

179986

show subpopulations

Gnomad4 AFR exome

AF:

0.00487

Gnomad4 AMR exome

AF:

0.0000733

Gnomad4 ASJ exome

AF:

0.00

Gnomad4 EAS exome

AF:

0.00

Gnomad4 SAS exome

AF:

0.0000335

Gnomad4 FIN exome

AF:

0.0000373

Gnomad4 NFE exome

AF:

0.0000126

Gnomad4 OTH exome

AF:

0.000140

GnomAD4 genome

AF:

0.00180

AC:

273

AN:

151374

Hom.:

Cov.:

AF XY:

0.00179

AC XY:

132

AN XY:

73924

show subpopulations

Gnomad4 AFR

AF:

0.00642

Gnomad4 AMR

AF:

0.000397

Gnomad4 ASJ

AF:

0.00

Gnomad4 EAS

AF:

0.00

Gnomad4 SAS

AF:

0.00

Gnomad4 FIN

AF:

0.00

Gnomad4 NFE

AF:

0.00

Gnomad4 OTH

AF:

0.000952

Alfa

AF:

0.000820

Hom.:

Bravo

AF:

0.00233

ExAC

AF:

0.000284

AC:

ClinVar

Significance: Likely benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

LINK: link

Submissions by phenotype

not provided

Benign:1

Likely benign, criteria provided, single submitter

clinical testing

CeGaT Center for Human Genetics Tuebingen

Sep 01, 2023

LDB3: BS1 -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_addAF

Benign

-0.46

BayesDel_noAF

Benign

-0.43

CADD

Benign

DANN

Uncertain

0.98

Eigen

Benign

-0.94

Eigen_PC

Benign

-0.96

FATHMM_MKL

Benign

0.036

LIST_S2

Benign

0.45

MetaRNN

Benign

0.0031

MetaSVM

Benign

-1.0

MutationTaster

Benign

1.0

PROVEAN

Benign

0.60

REVEL

Benign

0.071

Sift

Benign

0.19

Sift4G

Benign

0.17

Polyphen

0.0

MVP

0.19

ClinPred

0.0080

GERP RS

1.6

Splicing

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

Publications

LitVar

Below is the list of publications found by LitVar. It may be empty.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

LitVar

Other links and lift over