chr1-162378327-G-C

Variant names:

• chr1-162378327-G-C
• rs164041
• ENST00000420220.1:c.-11-3564G>C

Variant summary

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

The ENST00000420220.1(ENSG00000254706):​c.-11-3564G>C 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 152,208 control chromosomes in the GnomAD database, including 1,792 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 (1792 hom., cov: 32)
• Consequence: ENSG00000254706 ENST00000420220.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.309
• Publications: 5 publications found

Genes affected

ENSG00000254706 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.181 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000420220.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ENSG00000254706	ENST00000420220.1	TSL:5	c.-11-3564G>C		intron	N/A	ENSP00000398035.1
	ENSG00000254706	ENST00000431696.1	TSL:4	c.227-3564G>C		intron	N/A	ENSP00000405676.2
	ENSG00000254706	ENST00000367932.3	TSL:4	n.153-3564G>C		intron	N/A	ENSP00000356909.3

Frequencies

GnomAD3 genomes AF: 0.141 AC: 21419 AN: 152090 Hom.: 1790 Cov.: 32

Gnomad AFR AF: 0.0564

Gnomad AMI AF: 0.140

Gnomad AMR AF: 0.136

Gnomad ASJ AF: 0.273

Gnomad EAS AF: 0.0648

Gnomad SAS AF: 0.154

Gnomad FIN AF: 0.177

Gnomad MID AF: 0.304

Gnomad NFE AF: 0.184

Gnomad OTH AF: 0.182

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

GnomAD4 genome AF: 0.141 AC: 21425 AN: 152208 Hom.: 1792 Cov.: 32 AF XY: 0.140 AC XY: 10445 AN XY: 74422

African (AFR) AF: 0.0562 AC: 2336 AN: 41546

American (AMR) AF: 0.136 AC: 2080 AN: 15296

Ashkenazi Jewish (ASJ) AF: 0.273 AC: 948 AN: 3470

East Asian (EAS) AF: 0.0645 AC: 335 AN: 5192

South Asian (SAS) AF: 0.155 AC: 750 AN: 4824

European-Finnish (FIN) AF: 0.177 AC: 1870 AN: 10572

Middle Eastern (MID) AF: 0.313 AC: 92 AN: 294

European-Non Finnish (NFE) AF: 0.184 AC: 12498 AN: 67990

Other (OTH) AF: 0.184 AC: 388 AN: 2112

Alfa AF: 0.174 Hom.: 335

Bravo AF: 0.133

Asia WGS AF: 0.126 AC: 437 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	6.1
DANN	Benign	0.63
PhyloP100		-0.31

Splicing

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

Other links and lift over

dbSNP: rs164041; hg19: chr1-162348117;