1-24322926-C-T

Position:

• chr1-24322926-C-T

Variant summary

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

The NM_198173.3(GRHL3):​c.17+3358C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.116 in 624,322 control chromosomes in the GnomAD database, including 4,821 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

• Frequency:
  • Genomes: 𝑓 0.14 (1746 hom., cov: 32)
  • Exomes 𝑓: 0.11 (3075 hom.)
• Consequence: GRHL3 NM_198173.3 intron
• Clinical Significance: Benign criteria provided, multiple submitters, no conflicts B:2
• Conservation: PhyloP100: -0.827

Genes affected

GRHL3 (HGNC:25839): (grainyhead like transcription factor 3) This gene encodes a member of the grainyhead family of transcription factors. The encoded protein may function as a transcription factor during development, and has been shown to stimulate migration of endothelial cells. Multiple transcript variants encoding distinct isoforms have been identified for this gene.[provided by RefSeq, Aug 2010]

ACMG classification

Verdict is Benign. Variant got -20 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BP6: Variant 1-24322926-C-T is Benign according to our data. Variant chr1-24322926-C-T is described in ClinVar as [Benign]. Clinvar id is 1243060.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.221 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
GRHL3	NM_198173.3	c.17+3358C>T		intron_variant		ENST00000361548.9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
GRHL3	ENST00000361548.9	c.17+3358C>T		intron_variant		1	NM_198173.3	P1

Frequencies

GnomAD3 genomes AF: 0.139 AC: 21195 AN: 152056 Hom.: 1740 Cov.: 32

Gnomad AFR AF: 0.225

Gnomad AMI AF: 0.0987

Gnomad AMR AF: 0.0999

Gnomad ASJ AF: 0.0421

Gnomad EAS AF: 0.159

Gnomad SAS AF: 0.108

Gnomad FIN AF: 0.112

Gnomad MID AF: 0.0253

Gnomad NFE AF: 0.108

Gnomad OTH AF: 0.116

GnomAD4 exome AF: 0.109 AC: 51269 AN: 472148 Hom.: 3075 AF XY: 0.108 AC XY: 27113 AN XY: 249902

Gnomad4 AFR exome AF: 0.217

Gnomad4 AMR exome AF: 0.0962

Gnomad4 ASJ exome AF: 0.0429

Gnomad4 EAS exome AF: 0.127

Gnomad4 SAS exome AF: 0.103

Gnomad4 FIN exome AF: 0.113

Gnomad4 NFE exome AF: 0.106

Gnomad4 OTH exome AF: 0.114

GnomAD4 genome AF: 0.139 AC: 21207 AN: 152174 Hom.: 1746 Cov.: 32 AF XY: 0.136 AC XY: 10142 AN XY: 74390

Gnomad4 AFR AF: 0.224

Gnomad4 AMR AF: 0.100

Gnomad4 ASJ AF: 0.0421

Gnomad4 EAS AF: 0.159

Gnomad4 SAS AF: 0.108

Gnomad4 FIN AF: 0.112

Gnomad4 NFE AF: 0.108

Gnomad4 OTH AF: 0.114

Alfa AF: 0.121 Hom.: 572

Bravo AF: 0.144

Asia WGS AF: 0.136 AC: 472 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:2

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

not provided Benign:2

Benign, criteria provided, single submitter	clinical testing	GeneDx	May 12, 2021	- -
Benign, criteria provided, single submitter	not provided	Breakthrough Genomics, Breakthrough Genomics	-	- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	2.3
DANN	Benign	0.69

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: rs1324663; hg19: chr1-24649416; COSMIC: COSV52565504; COSMIC: COSV52565504;