rs7112844

Variant names:

• chr11-5230954-T-A
• rs7112844
• ENST00000759072.1:n.265+5226T>A

Your query was ambiguous. Multiple possible variants found:

• chr11-5230954-T-A
• chr11-5230954-T-C

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The ENST00000759072.1(ENSG00000298932):​n.265+5226T>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0972 in 152,030 control chromosomes in the GnomAD database, including 2,216 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 0.097 (2216 hom., cov: 31)
• Consequence: ENSG00000298932 ENST00000759072.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.13
• Publications: 2 publications found

Genes affected

ENSG00000298932 (HGNC:):

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.321 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
ENSG00000298932	ENST00000759072.1	n.265+5226T>A		intron_variant	Intron 1 of 1

Frequencies

GnomAD3 genomes AF: 0.0970 AC: 14736 AN: 151914 Hom.: 2206 Cov.: 31

Gnomad AFR AF: 0.326

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.0417

Gnomad ASJ AF: 0.00173

Gnomad EAS AF: 0.000386

Gnomad SAS AF: 0.00394

Gnomad FIN AF: 0.00339

Gnomad MID AF: 0.0253

Gnomad NFE AF: 0.00616

Gnomad OTH AF: 0.0789

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

GnomAD4 genome AF: 0.0972 AC: 14781 AN: 152030 Hom.: 2216 Cov.: 31 AF XY: 0.0934 AC XY: 6947 AN XY: 74354

African (AFR) AF: 0.326 AC: 13491 AN: 41382

American (AMR) AF: 0.0416 AC: 636 AN: 15274

Ashkenazi Jewish (ASJ) AF: 0.00173 AC: 6 AN: 3468

East Asian (EAS) AF: 0.000387 AC: 2 AN: 5174

South Asian (SAS) AF: 0.00373 AC: 18 AN: 4822

European-Finnish (FIN) AF: 0.00339 AC: 36 AN: 10608

Middle Eastern (MID) AF: 0.0272 AC: 8 AN: 294

European-Non Finnish (NFE) AF: 0.00616 AC: 419 AN: 67984

Other (OTH) AF: 0.0781 AC: 165 AN: 2112

Alfa AF: 0.00393 Hom.: 7

Bravo AF: 0.107

Asia WGS AF: 0.0220 AC: 78 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	1.5
DANN	Benign	0.68
PhyloP100		-1.1

Splicing

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

Other links and lift over

dbSNP: rs7112844; hg19: chr11-5252184;