ENST00000505200.1:n.213-4415A>G

Variant names:

• chr5-74992038-T-C
• rs7707833
• ENST00000505200.1:n.213-4415A>G

Variant summary

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

The ENST00000505200.1(ENSG00000249856):​n.213-4415A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.501 in 151,954 control chromosomes in the GnomAD database, including 20,860 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 0.50 (20860 hom., cov: 31)
• Consequence: ENSG00000249856 ENST00000505200.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.655

Genes affected

ENSG00000249856 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.746 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ENSG00000249856	ENST00000505200.1	n.213-4415A>G		intron_variant	Intron 2 of 4	3

Frequencies

GnomAD3 genomes AF: 0.500 AC: 75945 AN: 151836 Hom.: 20814 Cov.: 31

Gnomad AFR AF: 0.753

Gnomad AMI AF: 0.485

Gnomad AMR AF: 0.426

Gnomad ASJ AF: 0.404

Gnomad EAS AF: 0.379

Gnomad SAS AF: 0.375

Gnomad FIN AF: 0.420

Gnomad MID AF: 0.443

Gnomad NFE AF: 0.400

Gnomad OTH AF: 0.458

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

GnomAD4 genome AF: 0.501 AC: 76055 AN: 151954 Hom.: 20860 Cov.: 31 AF XY: 0.497 AC XY: 36940 AN XY: 74276

Gnomad4 AFR AF: 0.753

Gnomad4 AMR AF: 0.425

Gnomad4 ASJ AF: 0.404

Gnomad4 EAS AF: 0.380

Gnomad4 SAS AF: 0.375

Gnomad4 FIN AF: 0.420

Gnomad4 NFE AF: 0.401

Gnomad4 OTH AF: 0.460

Alfa AF: 0.450 Hom.: 3453

Bravo AF: 0.515

Asia WGS AF: 0.410 AC: 1426 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	0.52
DANN	Benign	0.59

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs7707833; hg19: chr5-74287863;