chr11-131824982-A-C

Variant names:

• chr11-131824982-A-C
• rs576825
• NM_001352005.2:c.83-86582A>C

Variant summary

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

The NM_001352005.2(NTM):​c.83-86582A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.366 in 152,072 control chromosomes in the GnomAD database, including 10,607 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 0.37 (10607 hom., cov: 32)
• Consequence: NTM NM_001352005.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.13
• Publications: 1 publications found

Genes affected

NTM (HGNC:17941): (neurotrimin) This gene encodes a member of the IgLON (LAMP, OBCAM, Ntm) family of immunoglobulin (Ig) domain-containing glycosylphosphatidylinositol (GPI)-anchored cell adhesion molecules. The encoded protein may promote neurite outgrowth and adhesion via a homophilic mechanism. This gene is closely linked to a related family member, opioid binding protein/cell adhesion molecule-like (OPCML), on chromosome 11. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2009]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.456 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001352005.2. 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
	NTM	NM_001352005.2	MANE Select	c.83-86582A>C		intron	N/A	NP_001338934.1	B7Z1Z5
	NTM	NM_001352001.2		c.83-86582A>C		intron	N/A	NP_001338930.1
	NTM	NM_001352003.2		c.83-86582A>C		intron	N/A	NP_001338932.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	NTM	ENST00000683400.1	MANE Select	c.83-86582A>C		intron	N/A	ENSP00000507313.1	B7Z1Z5
	NTM	ENST00000374791.7	TSL:1	c.83-86582A>C		intron	N/A	ENSP00000363923.3	Q9P121-2
	NTM	ENST00000550167.5	TSL:5	c.56-86582A>C		intron	N/A	ENSP00000448104.1	F8VTR5

Frequencies

GnomAD3 genomes AF: 0.366 AC: 55563 AN: 151954 Hom.: 10598 Cov.: 32

Gnomad AFR AF: 0.460

Gnomad AMI AF: 0.410

Gnomad AMR AF: 0.347

Gnomad ASJ AF: 0.372

Gnomad EAS AF: 0.144

Gnomad SAS AF: 0.472

Gnomad FIN AF: 0.322

Gnomad MID AF: 0.361

Gnomad NFE AF: 0.328

Gnomad OTH AF: 0.359

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

GnomAD4 genome AF: 0.366 AC: 55603 AN: 152072 Hom.: 10607 Cov.: 32 AF XY: 0.367 AC XY: 27275 AN XY: 74332

African (AFR) AF: 0.459 AC: 19045 AN: 41474

American (AMR) AF: 0.347 AC: 5294 AN: 15270

Ashkenazi Jewish (ASJ) AF: 0.372 AC: 1292 AN: 3472

East Asian (EAS) AF: 0.144 AC: 742 AN: 5164

South Asian (SAS) AF: 0.472 AC: 2274 AN: 4814

European-Finnish (FIN) AF: 0.322 AC: 3415 AN: 10590

Middle Eastern (MID) AF: 0.371 AC: 109 AN: 294

European-Non Finnish (NFE) AF: 0.328 AC: 22300 AN: 67970

Other (OTH) AF: 0.359 AC: 760 AN: 2116

Alfa AF: 0.340 Hom.: 38716

Bravo AF: 0.365

Asia WGS AF: 0.328 AC: 1145 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	1.8
DANN	Benign	0.33
PhyloP100		-1.1
Mutation Taster		=100/0	polymorphism (auto)

Splicing

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

Other links and lift over

dbSNP: rs576825; hg19: chr11-131694876;