rs6830890

Variant names:

• chr4-111597970-G-A
• rs6830890
• ENST00000681880.1:n.171-20535G>A

Variant summary

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

The ENST00000681880.1(ENSG00000248656):​n.171-20535G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.117 in 151,728 control chromosomes in the GnomAD database, including 1,275 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 0.12 (1275 hom., cov: 31)
• Consequence: ENSG00000248656 ENST00000681880.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.19
• Publications: 3 publications found

Genes affected

ENSG00000248656 (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 (EAS) allele frequency at 95% confidence interval = 0.194 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000681880.1. 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
	ENSG00000248656	ENST00000681880.1		n.171-20535G>A		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.117 AC: 17767 AN: 151610 Hom.: 1268 Cov.: 31

Gnomad AFR AF: 0.0442

Gnomad AMI AF: 0.264

Gnomad AMR AF: 0.168

Gnomad ASJ AF: 0.0761

Gnomad EAS AF: 0.205

Gnomad SAS AF: 0.202

Gnomad FIN AF: 0.202

Gnomad MID AF: 0.0538

Gnomad NFE AF: 0.125

Gnomad OTH AF: 0.101

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

GnomAD4 genome AF: 0.117 AC: 17786 AN: 151728 Hom.: 1275 Cov.: 31 AF XY: 0.124 AC XY: 9212 AN XY: 74104

African (AFR) AF: 0.0442 AC: 1832 AN: 41416

American (AMR) AF: 0.169 AC: 2577 AN: 15242

Ashkenazi Jewish (ASJ) AF: 0.0761 AC: 264 AN: 3470

East Asian (EAS) AF: 0.205 AC: 1046 AN: 5112

South Asian (SAS) AF: 0.202 AC: 972 AN: 4814

European-Finnish (FIN) AF: 0.202 AC: 2111 AN: 10434

Middle Eastern (MID) AF: 0.0510 AC: 15 AN: 294

European-Non Finnish (NFE) AF: 0.125 AC: 8519 AN: 67932

Other (OTH) AF: 0.0997 AC: 210 AN: 2106

Alfa AF: 0.120 Hom.: 1786

Bravo AF: 0.110

Asia WGS AF: 0.164 AC: 569 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	5.4
DANN	Benign	0.77
PhyloP100		1.2

Splicing

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

Other links and lift over

dbSNP: rs6830890; hg19: chr4-112519126;