chr9-127452135-C-T

Position:

• chr9-127452135-C-T

Variant summary

Our verdict is Benign. Variant got -20 ACMG points: 0P and 20B. BP4_Strong BP6_Very_Strong BA1

The NM_001005373.4(LRSAM1):​c.-33+51C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.105 in 152,300 control chromosomes in the GnomAD database, including 1,342 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

• Frequency:
  • Genomes: 𝑓 0.10 (1342 hom., cov: 32)
  • Exomes 𝑓: 0.034 (0 hom.)
• Consequence: LRSAM1 NM_001005373.4 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -3.31

Genes affected

LRSAM1 (HGNC:25135): (leucine rich repeat and sterile alpha motif containing 1) This gene encodes a ring finger protein involved in a variety of functions, including regulation of signaling pathways and cell adhesion, mediation of self-ubiquitylation, and involvement in cargo sorting during receptor endocytosis. Mutations in this gene have been associated with Charcot-Marie-Tooth disease. Multiple transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jan 2012]

ACMG classification

Verdict is Benign. Variant got -20 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BP6: Variant 9-127452135-C-T is Benign according to our data. Variant chr9-127452135-C-T is described in ClinVar as [Benign]. Clinvar id is 674025.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.267 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
LRSAM1	NM_001005373.4	c.-33+51C>T		intron_variant		ENST00000300417.11

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
LRSAM1	ENST00000300417.11	c.-33+51C>T		intron_variant		1	NM_001005373.4	P1

Frequencies

GnomAD3 genomes AF: 0.105 AC: 15952 AN: 152124 Hom.: 1333 Cov.: 32

Gnomad AFR AF: 0.0375

Gnomad AMI AF: 0.112

Gnomad AMR AF: 0.274

Gnomad ASJ AF: 0.127

Gnomad EAS AF: 0.204

Gnomad SAS AF: 0.147

Gnomad FIN AF: 0.0938

Gnomad MID AF: 0.111

Gnomad NFE AF: 0.0974

Gnomad OTH AF: 0.125

GnomAD4 exome AF: 0.0345 AC: 2 AN: 58 Hom.: 0 Cov.: 0 AF XY: 0.0227 AC XY: 1 AN XY: 44

Gnomad4 SAS exome AF: 0.00

Gnomad4 FIN exome AF: 0.0833

Gnomad4 NFE exome AF: 0.0250

Gnomad4 OTH exome AF: 0.00

GnomAD4 genome AF: 0.105 AC: 15973 AN: 152242 Hom.: 1342 Cov.: 32 AF XY: 0.109 AC XY: 8139 AN XY: 74436

Gnomad4 AFR AF: 0.0375

Gnomad4 AMR AF: 0.274

Gnomad4 ASJ AF: 0.127

Gnomad4 EAS AF: 0.205

Gnomad4 SAS AF: 0.147

Gnomad4 FIN AF: 0.0938

Gnomad4 NFE AF: 0.0974

Gnomad4 OTH AF: 0.123

Alfa AF: 0.0487 Hom.: 49

Bravo AF: 0.122

Asia WGS AF: 0.149 AC: 518 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Jun 20, 2018

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	6.2
DANN	Benign	0.82
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.1

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

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

Publications

LitVar

Other links and lift over

dbSNP: rs3808831; hg19: chr9-130214414;