Variant 16-15036083-C-T details in Genebe, Genetics Data Aggregator

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_StrongBP6BP7BA1

The NM_015027.4(PDXDC1):c.2175C>T(p.His725=) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.363 in 1,613,794 control chromosomes in the GnomAD database, including 115,870 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (no stars).

Frequency

Genomes: 𝑓 0.28 ( 7872 hom., cov: 32)

Exomes 𝑓: 0.37 ( 107998 hom. )

Consequence

PDXDC1
NM_015027.4 synonymous

Scores

Clinical Significance

Benign no assertion criteria provided B:1

Conservation

PhyloP100: -0.0700

Variant links:

Genes affected

PDXDC1 (HGNC:28995): (pyridoxal dependent decarboxylase domain containing 1) Enables cadherin binding activity. Predicted to be involved in carboxylic acid metabolic process. Located in Golgi apparatus. [provided by Alliance of Genome Resources, Apr 2022]

PDXDC1 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 (BayesDel_noAF=-0.62).

BP6

Variant 16-15036083-C-T is Benign according to our data. Variant chr16-15036083-C-T is described in ClinVar as [Benign]. Clinvar id is 3060524.Status of the report is no_assertion_criteria_provided, 0 stars.

BP7

Synonymous conserved (PhyloP=-0.07 with no splicing effect.

BA1

GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.404 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
PDXDC1	NM_015027.4 linkuse as main transcript	c.2175C>T	p.His725=	synonymous_variant	23/23	ENST00000396410.9	NP_055842.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
PDXDC1	ENST00000396410.9 linkuse as main transcript	c.2175C>T	p.His725=	synonymous_variant	23/23	1	NM_015027.4	ENSP00000379691	P1	Q6P996-1

Frequencies

GnomAD3 genomes

AF:

0.282

AC:

42853

AN:

152004

Hom.:

7874

Cov.:

show subpopulations

Gnomad AFR

AF:

0.0753

Gnomad AMI

AF:

0.552

Gnomad AMR

AF:

0.255

Gnomad ASJ

AF:

0.391

Gnomad EAS

AF:

0.00347

Gnomad SAS

AF:

0.250

Gnomad FIN

AF:

0.400

Gnomad MID

AF:

0.418

Gnomad NFE

AF:

0.408

Gnomad OTH

AF:

0.311

GnomAD3 exomes

AF:

0.307

AC:

77081

AN:

251280

Hom.:

14382

AF XY:

0.320

AC XY:

43431

AN XY:

135826

show subpopulations

Gnomad AFR exome

AF:

0.0684

Gnomad AMR exome

AF:

0.183

Gnomad ASJ exome

AF:

0.386

Gnomad EAS exome

AF:

0.00228

Gnomad SAS exome

AF:

0.260

Gnomad FIN exome

AF:

0.394

Gnomad NFE exome

AF:

0.414

Gnomad OTH exome

AF:

0.358

GnomAD4 exome

AF:

0.371

AC:

542601

AN:

1461672

Hom.:

107998

Cov.:

AF XY:

0.370

AC XY:

269110

AN XY:

727148

show subpopulations

Gnomad4 AFR exome

AF:

0.0658

Gnomad4 AMR exome

AF:

0.191

Gnomad4 ASJ exome

AF:

0.381

Gnomad4 EAS exome

AF:

0.00209

Gnomad4 SAS exome

AF:

0.265

Gnomad4 FIN exome

AF:

0.404

Gnomad4 NFE exome

AF:

0.408

Gnomad4 OTH exome

AF:

0.351

GnomAD4 genome

AF:

0.282

AC:

42838

AN:

152122

Hom.:

7872

Cov.:

AF XY:

0.278

AC XY:

20699

AN XY:

74366

show subpopulations

Gnomad4 AFR

AF:

0.0750

Gnomad4 AMR

AF:

0.254

Gnomad4 ASJ

AF:

0.391

Gnomad4 EAS

AF:

0.00348

Gnomad4 SAS

AF:

0.250

Gnomad4 FIN

AF:

0.400

Gnomad4 NFE

AF:

0.408

Gnomad4 OTH

AF:

0.308

Alfa

AF:

0.374

Hom.:

19629

Bravo

AF:

0.260

Asia WGS

AF:

0.108

AC:

380

AN:

3478

EpiCase

AF:

0.413

EpiControl

AF:

0.426

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: no assertion criteria provided

LINK: link

Submissions by phenotype

PDXDC1-related disorder

Benign:1

Benign, no assertion criteria provided

clinical testing

PreventionGenetics, part of Exact Sciences

Oct 16, 2019

This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.62

CADD

Benign

8.6

DANN

Benign

0.80

RBP_binding_hub_radar

0.0

RBP_regulation_power_radar

1.1

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

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