rs11208184

Variant names:

• chr1-63308530-G-A
• rs11208184
• ENST00000436475.3:n.314-3784C>T

Your query was ambiguous. Multiple possible variants found:

• chr1-63308530-G-A
• chr1-63308530-G-T

Variant summary

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

The ENST00000436475.3(LINC00466):​n.314-3784C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.079 in 152,130 control chromosomes in the GnomAD database, including 564 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 0.079 (564 hom., cov: 32)
• Consequence: LINC00466 ENST00000436475.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0130
• Publications: 0 publications found

Genes affected

LINC00466 (HGNC:27294): (long intergenic non-protein coding RNA 466)

ENSG00000293613 (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 (EAS) allele frequency at 95% confidence interval = 0.17 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
LINC00466	NR_038252.3	n.340-3784C>T		intron_variant	Intron 2 of 11

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
LINC00466	ENST00000436475.3	n.314-3784C>T		intron_variant	Intron 2 of 6	5
LINC00466	ENST00000447183.3	n.39-3784C>T		intron_variant	Intron 1 of 6	5
LINC00466	ENST00000455304.6	n.140-3784C>T		intron_variant	Intron 1 of 4	5

Frequencies

GnomAD3 genomes AF: 0.0790 AC: 12014 AN: 152012 Hom.: 563 Cov.: 32

Gnomad AFR AF: 0.0509

Gnomad AMI AF: 0.0495

Gnomad AMR AF: 0.133

Gnomad ASJ AF: 0.0605

Gnomad EAS AF: 0.180

Gnomad SAS AF: 0.106

Gnomad FIN AF: 0.0746

Gnomad MID AF: 0.101

Gnomad NFE AF: 0.0762

Gnomad OTH AF: 0.0876

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

GnomAD4 genome AF: 0.0790 AC: 12015 AN: 152130 Hom.: 564 Cov.: 32 AF XY: 0.0814 AC XY: 6053 AN XY: 74350

African (AFR) AF: 0.0508 AC: 2111 AN: 41526

American (AMR) AF: 0.133 AC: 2031 AN: 15276

Ashkenazi Jewish (ASJ) AF: 0.0605 AC: 210 AN: 3470

East Asian (EAS) AF: 0.180 AC: 929 AN: 5162

South Asian (SAS) AF: 0.106 AC: 512 AN: 4814

European-Finnish (FIN) AF: 0.0746 AC: 790 AN: 10594

Middle Eastern (MID) AF: 0.0952 AC: 28 AN: 294

European-Non Finnish (NFE) AF: 0.0761 AC: 5176 AN: 67974

Other (OTH) AF: 0.0867 AC: 183 AN: 2110

Alfa AF: 0.0764 Hom.: 1365

Bravo AF: 0.0834

Asia WGS AF: 0.118 AC: 409 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	1.8
DANN	Benign	0.69
PhyloP100		0.013

Splicing

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

Other links and lift over

dbSNP: rs11208184; hg19: chr1-63774201;