rs73118372

Positions:

• chr3-9943989-T-C
• chr3-9943989-T-G

Variant summary

Our verdict is Benign. Variant got -20 ACMG points: 0P and 20B. BP4_Strong BP6_Very_Strong BA1

The NM_001374317.1(CRELD1):​c.1148T>C​(p.Met383Thr) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.021 in 1,036,400 control chromosomes in the GnomAD database, including 1,683 homozygotes. In-silico tool predicts a benign outcome for this variant. 13/17 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

• Frequency:
  • Genomes: 𝑓 0.065 (939 hom., cov: 32)
  • Exomes 𝑓: 0.013 (744 hom.)
• Consequence: CRELD1 NM_001374317.1 missense
• Clinical Significance: Benign criteria provided, multiple submitters, no conflicts B:3
• Conservation: PhyloP100: -0.304

Genes affected

CRELD1 (HGNC:14630): (cysteine rich with EGF like domains 1) This gene encodes a member of a subfamily of epidermal growth factor-related proteins. The encoded protein is characterized by a cysteine-rich with epidermal growth factor-like domain. This protein may function as a cell adhesion molecule. Mutations in this gene are the cause of atrioventricular septal defect. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2010]

ENSG00000288550 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -20 ACMG points.

• BP4: Computational evidence support a benign effect (MetaRNN=0.0027036965).
• BP6: Variant 3-9943989-T-C is Benign according to our data. Variant chr3-9943989-T-C is described in ClinVar as [Benign]. Clinvar id is 137031.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.212 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
CRELD1	NM_001077415.3	c.1049-376T>C		intron_variant		ENST00000452070.6	NP_001070883.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
CRELD1	ENST00000452070.6	c.1049-376T>C		intron_variant		2	NM_001077415.3	ENSP00000393643.2
ENSG00000288550	ENST00000683484.1	n.*697-376T>C		intron_variant				ENSP00000507040.1

Frequencies

GnomAD3 genomes AF: 0.0650 AC: 9880 AN: 152004 Hom.: 933 Cov.: 32

Gnomad AFR AF: 0.215

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.0291

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.0241

Gnomad SAS AF: 0.0484

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.0316

Gnomad NFE AF: 0.000912

Gnomad OTH AF: 0.0512

GnomAD3 exomes AF: 0.0264 AC: 6568 AN: 249054 Hom.: 439 AF XY: 0.0229 AC XY: 3094 AN XY: 134818

Gnomad AFR exome AF: 0.224

Gnomad AMR exome AF: 0.0303

Gnomad ASJ exome AF: 0.00

Gnomad EAS exome AF: 0.0253

Gnomad SAS exome AF: 0.0403

Gnomad FIN exome AF: 0.000139

Gnomad NFE exome AF: 0.000925

Gnomad OTH exome AF: 0.0121

GnomAD4 exome AF: 0.0134 AC: 11835 AN: 884278 Hom.: 744 Cov.: 13 AF XY: 0.0133 AC XY: 6162 AN XY: 463528

Gnomad4 AFR exome AF: 0.229

Gnomad4 AMR exome AF: 0.0312

Gnomad4 ASJ exome AF: 0.0000444

Gnomad4 EAS exome AF: 0.0208

Gnomad4 SAS exome AF: 0.0406

Gnomad4 FIN exome AF: 0.000207

Gnomad4 NFE exome AF: 0.000625

Gnomad4 OTH exome AF: 0.0224

GnomAD4 genome AF: 0.0652 AC: 9917 AN: 152122 Hom.: 939 Cov.: 32 AF XY: 0.0631 AC XY: 4689 AN XY: 74356

Gnomad4 AFR AF: 0.215

Gnomad4 AMR AF: 0.0293

Gnomad4 ASJ AF: 0.00

Gnomad4 EAS AF: 0.0241

Gnomad4 SAS AF: 0.0479

Gnomad4 FIN AF: 0.00

Gnomad4 NFE AF: 0.000912

Gnomad4 OTH AF: 0.0526

Alfa AF: 0.00947 Hom.: 191

Bravo AF: 0.0748

TwinsUK AF: 0.000270 AC: 1

ALSPAC AF: 0.000778 AC: 3

ESP6500AA AF: 0.210 AC: 927

ESP6500EA AF: 0.00105 AC: 9

ExAC AF: 0.0297 AC: 3608

Asia WGS AF: 0.0350 AC: 123 AN: 3478

EpiCase AF: 0.00131

EpiControl AF: 0.000771

ClinVar

Significance: Benign

Submissions summary: Benign:3

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

not specified Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Oct 01, 2013

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. -

Atrioventricular septal defect, susceptibility to, 2 Benign:1

Benign, criteria provided, single submitter

clinical testing

Labcorp Genetics (formerly Invitae), Labcorp

Jan 29, 2024

- -

not provided Benign:1

Benign, criteria provided, single submitter

not provided

Breakthrough Genomics, Breakthrough Genomics

-

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_addAF	Benign	-0.75	T
BayesDel_noAF	Benign	-0.71
CADD	Benign	2.7
DANN	Benign	0.53
Eigen	Benign	-1.2
Eigen_PC	Benign	-1.3
FATHMM_MKL	Benign	0.0019	N
LIST_S2	Benign	0.18	T
MetaRNN	Benign	0.0027	T
MetaSVM	Benign	-1.0	T
PrimateAI	Benign	0.29	T
PROVEAN	Benign	1.2	N
REVEL	Benign	0.051
Sift	Benign	1.0	T
Sift4G	Benign	0.75	T
Polyphen		0.0	B
Vest4		0.027
MPC		0.18
ClinPred		0.000023	T
GERP RS		1.7
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.0
gMVP		0.49

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs73118372; hg19: chr3-9985673;