chr2-149833000-C-T

Variant names:

• chr2-149833000-C-T
• rs4132253
• ENST00000295052.3:n.1302+24451G>A

Variant summary

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

The ENST00000295052.3(LINC01931):​n.1302+24451G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.15 in 151,944 control chromosomes in the GnomAD database, including 2,176 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 0.15 (2176 hom., cov: 32)
• Consequence: LINC01931 ENST00000295052.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0700
• Publications: 2 publications found

Genes affected

LINC01931 (HGNC:52743): (long intergenic non-protein coding RNA 1931)

MMADHC-DT (HGNC:41087): (MMADHC divergent transcript)

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 = 0.441 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000295052.3. 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
	MMADHC-DT	NR_110240.1		n.536-14909C>T		intron	N/A
	LINC01931	NR_145421.1		n.1302+24451G>A		intron	N/A

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LINC01931	ENST00000295052.3	TSL:2	n.1302+24451G>A		intron	N/A
	LINC01931	ENST00000433174.1	TSL:2	n.236-16216G>A		intron	N/A
	MMADHC-DT	ENST00000449714.3	TSL:2	n.611-14909C>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.150 AC: 22805 AN: 151826 Hom.: 2172 Cov.: 32

Gnomad AFR AF: 0.0671

Gnomad AMI AF: 0.0725

Gnomad AMR AF: 0.205

Gnomad ASJ AF: 0.195

Gnomad EAS AF: 0.457

Gnomad SAS AF: 0.166

Gnomad FIN AF: 0.157

Gnomad MID AF: 0.165

Gnomad NFE AF: 0.162

Gnomad OTH AF: 0.161

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

GnomAD4 genome AF: 0.150 AC: 22808 AN: 151944 Hom.: 2176 Cov.: 32 AF XY: 0.152 AC XY: 11274 AN XY: 74248

African (AFR) AF: 0.0671 AC: 2784 AN: 41466

American (AMR) AF: 0.205 AC: 3116 AN: 15234

Ashkenazi Jewish (ASJ) AF: 0.195 AC: 677 AN: 3466

East Asian (EAS) AF: 0.457 AC: 2342 AN: 5126

South Asian (SAS) AF: 0.165 AC: 795 AN: 4814

European-Finnish (FIN) AF: 0.157 AC: 1655 AN: 10572

Middle Eastern (MID) AF: 0.163 AC: 48 AN: 294

European-Non Finnish (NFE) AF: 0.162 AC: 10983 AN: 67954

Other (OTH) AF: 0.162 AC: 342 AN: 2108

Alfa AF: 0.0972 Hom.: 247

Bravo AF: 0.153

Asia WGS AF: 0.316 AC: 1095 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	2.6
DANN	Benign	0.49
PhyloP100		-0.070

Splicing

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

Other links and lift over

dbSNP: rs4132253; hg19: chr2-150689514;