rs1374952

chr4-132986110-G-Achr4-132986110-G-T

Variant summary

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

The ENST00000511916.2(ENSG00000249513):n.251-302C>T variant causes a intron, non coding transcript change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0333 in 152,044 control chromosomes in the GnomAD database, including 198 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 0.033 (198 hom., cov: 32)
• Consequence: ENST00000511916.2 intron, non_coding_transcript
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.61

Genes affected

(HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.81).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.0932 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
	ENST00000511916.2	n.251-302C>T		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes AF: 0.0332 AC: 5042 AN: 151944 Hom.: 198 Cov.: 32

Gnomad AFR AF: 0.0954

Gnomad AMI AF: 0.00219

Gnomad AMR AF: 0.0170

Gnomad ASJ AF: 0.0257

Gnomad EAS AF: 0.0264

Gnomad SAS AF: 0.0106

Gnomad FIN AF: 0.00189

Gnomad MID AF: 0.0253

Gnomad NFE AF: 0.00697

Gnomad OTH AF: 0.0282

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

GnomAD4 genome AF: 0.0333 AC: 5057 AN: 152044 Hom.: 198 Cov.: 32 AF XY: 0.0314 AC XY: 2337 AN XY: 74320

Gnomad4 AFR AF: 0.0956

Gnomad4 AMR AF: 0.0169

Gnomad4 ASJ AF: 0.0257

Gnomad4 EAS AF: 0.0264

Gnomad4 SAS AF: 0.00997

Gnomad4 FIN AF: 0.00189

Gnomad4 NFE AF: 0.00697

Gnomad4 OTH AF: 0.0279

Alfa AF: 0.00259 Hom.: 1

Bravo AF: 0.0377

Asia WGS AF: 0.0420 AC: 147 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.81
Cadd	Benign	8.3
Dann	Benign	0.52

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs1374952; hg19: chr4-133907265;