rs4999939

Variant names:

• chr11-81231337-A-C
• rs4999939
• ENST00000671134.1:n.324-43539A>C

Your query was ambiguous. Multiple possible variants found:

• chr11-81231337-A-C
• chr11-81231337-A-G
• chr11-81231337-A-T

Variant summary

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

The ENST00000671134.1(ENSG00000287912):​n.324-43539A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.53 in 151,806 control chromosomes in the GnomAD database, including 23,485 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 0.53 (23485 hom., cov: 32)
• Consequence: ENSG00000287912 ENST00000671134.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.655
• Publications: 1 publications found

Genes affected

ENSG00000287912 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.95).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.915 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000671134.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
There are no transcript annotations for this variant.

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ENSG00000287912	ENST00000671134.1		n.324-43539A>C		intron	N/A
	ENSG00000287912	ENST00000671210.1		n.310-43539A>C		intron	N/A
	ENSG00000287912	ENST00000701193.2		n.196-43539A>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.529 AC: 80295 AN: 151688 Hom.: 23428 Cov.: 32

Gnomad AFR AF: 0.735

Gnomad AMI AF: 0.262

Gnomad AMR AF: 0.589

Gnomad ASJ AF: 0.442

Gnomad EAS AF: 0.937

Gnomad SAS AF: 0.489

Gnomad FIN AF: 0.363

Gnomad MID AF: 0.465

Gnomad NFE AF: 0.397

Gnomad OTH AF: 0.544

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

GnomAD4 genome AF: 0.530 AC: 80408 AN: 151806 Hom.: 23485 Cov.: 32 AF XY: 0.531 AC XY: 39370 AN XY: 74196

African (AFR) AF: 0.735 AC: 30443 AN: 41408

American (AMR) AF: 0.589 AC: 8957 AN: 15204

Ashkenazi Jewish (ASJ) AF: 0.442 AC: 1534 AN: 3468

East Asian (EAS) AF: 0.937 AC: 4816 AN: 5138

South Asian (SAS) AF: 0.487 AC: 2348 AN: 4824

European-Finnish (FIN) AF: 0.363 AC: 3824 AN: 10546

Middle Eastern (MID) AF: 0.463 AC: 136 AN: 294

European-Non Finnish (NFE) AF: 0.397 AC: 26955 AN: 67904

Other (OTH) AF: 0.548 AC: 1156 AN: 2108

Alfa AF: 0.444 Hom.: 26550

Bravo AF: 0.559

Asia WGS AF: 0.742 AC: 2578 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.95
CADD	Benign	2.5
DANN	Benign	0.81
PhyloP100		-0.66

Splicing

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

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

Other links and lift over

dbSNP: rs4999939;

hg19: chr11-80942380;