ENST00000667782.1:n.82+59773C>A

Variant names:

• chr2-78230615-G-T
• rs6547194
• ENST00000667782.1:n.82+59773C>A

Variant summary

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

The ENST00000667782.1(ENSG00000227088):​n.82+59773C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.141 in 151,812 control chromosomes in the GnomAD database, including 3,565 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 0.14 (3565 hom., cov: 32)
• Consequence: ENSG00000227088 ENST00000667782.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0570
• Publications: 2 publications found

Genes affected

ENSG00000227088 (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 (AFR) allele frequency at 95% confidence interval = 0.401 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000667782.1. 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
	LOC101927967	NR_110288.1		n.344+59773C>A		intron	N/A

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ENSG00000227088	ENST00000667782.1		n.82+59773C>A		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.141 AC: 21401 AN: 151696 Hom.: 3556 Cov.: 32

Gnomad AFR AF: 0.407

Gnomad AMI AF: 0.0471

Gnomad AMR AF: 0.0833

Gnomad ASJ AF: 0.0665

Gnomad EAS AF: 0.00116

Gnomad SAS AF: 0.0265

Gnomad FIN AF: 0.0154

Gnomad MID AF: 0.130

Gnomad NFE AF: 0.0370

Gnomad OTH AF: 0.110

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

GnomAD4 genome AF: 0.141 AC: 21435 AN: 151812 Hom.: 3565 Cov.: 32 AF XY: 0.135 AC XY: 10019 AN XY: 74204

African (AFR) AF: 0.406 AC: 16818 AN: 41382

American (AMR) AF: 0.0831 AC: 1263 AN: 15202

Ashkenazi Jewish (ASJ) AF: 0.0665 AC: 230 AN: 3460

East Asian (EAS) AF: 0.000971 AC: 5 AN: 5150

South Asian (SAS) AF: 0.0268 AC: 129 AN: 4818

European-Finnish (FIN) AF: 0.0154 AC: 163 AN: 10596

Middle Eastern (MID) AF: 0.136 AC: 40 AN: 294

European-Non Finnish (NFE) AF: 0.0370 AC: 2513 AN: 67892

Other (OTH) AF: 0.110 AC: 231 AN: 2106

Alfa AF: 0.0593 Hom.: 1116

Bravo AF: 0.158

Asia WGS AF: 0.0440 AC: 152 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	0.28
DANN	Benign	0.26
PhyloP100		0.057

Splicing

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

Other links and lift over

dbSNP: rs6547194; hg19: chr2-78457741;