NM_020911.2:c.3874+1736C>T

Variant names:

• chr7-132177951-G-A
• rs3734991
• NM_020911.2:c.3874+1736C>T

Variant summary

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

The NM_020911.2(PLXNA4):​c.3874+1736C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.287 in 151,946 control chromosomes in the GnomAD database, including 6,630 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 0.29 (6630 hom., cov: 32)
• Consequence: PLXNA4 NM_020911.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.122
• Publications: 4 publications found

Genes affected

PLXNA4 (HGNC:9102): (plexin A4) Predicted to enable semaphorin receptor activity. Predicted to be involved in several processes, including axon guidance; positive regulation of axonogenesis; and regulation of GTPase activity. Predicted to act upstream of or within several processes, including nervous system development; regulation of axon extension involved in axon guidance; and regulation of negative chemotaxis. Predicted to be located in plasma membrane. Predicted to be part of semaphorin receptor complex. Predicted to be integral component of plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.76).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.36 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_020911.2. 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
	PLXNA4	NM_020911.2	MANE Select	c.3874+1736C>T		intron	N/A	NP_065962.1
	PLXNA4	NM_001393897.1		c.3874+1736C>T		intron	N/A	NP_001380826.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PLXNA4	ENST00000321063.9	TSL:5 MANE Select	c.3874+1736C>T		intron	N/A	ENSP00000323194.4
	PLXNA4	ENST00000359827.7	TSL:5	c.3874+1736C>T		intron	N/A	ENSP00000352882.3

Frequencies

GnomAD3 genomes AF: 0.287 AC: 43565 AN: 151828 Hom.: 6617 Cov.: 32

Gnomad AFR AF: 0.364

Gnomad AMI AF: 0.0901

Gnomad AMR AF: 0.351

Gnomad ASJ AF: 0.229

Gnomad EAS AF: 0.269

Gnomad SAS AF: 0.372

Gnomad FIN AF: 0.206

Gnomad MID AF: 0.329

Gnomad NFE AF: 0.238

Gnomad OTH AF: 0.309

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

GnomAD4 genome AF: 0.287 AC: 43611 AN: 151946 Hom.: 6630 Cov.: 32 AF XY: 0.289 AC XY: 21484 AN XY: 74248

African (AFR) AF: 0.364 AC: 15068 AN: 41418

American (AMR) AF: 0.352 AC: 5370 AN: 15272

Ashkenazi Jewish (ASJ) AF: 0.229 AC: 793 AN: 3468

East Asian (EAS) AF: 0.269 AC: 1386 AN: 5148

South Asian (SAS) AF: 0.374 AC: 1793 AN: 4792

European-Finnish (FIN) AF: 0.206 AC: 2181 AN: 10580

Middle Eastern (MID) AF: 0.323 AC: 95 AN: 294

European-Non Finnish (NFE) AF: 0.238 AC: 16191 AN: 67954

Other (OTH) AF: 0.309 AC: 652 AN: 2110

Alfa AF: 0.259 Hom.: 4136

Bravo AF: 0.298

Asia WGS AF: 0.343 AC: 1191 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.76
CADD	Benign	4.5
DANN	Benign	0.77
PhyloP100		-0.12
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs3734991; hg19: chr7-131862710;