chr2-107987811-A-G

Position:

• chr2-107987811-A-G

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_Strong BP6_Moderate BA1

The NM_021815.5(SLC5A7):​c.-51-294A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.042 in 152,294 control chromosomes in the GnomAD database, including 166 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency: Genomes: 𝑓 0.042 (166 hom., cov: 33)
• Consequence: SLC5A7 NM_021815.5 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: 0.179

Genes affected

SLC5A7 (HGNC:14025): (solute carrier family 5 member 7) This gene encodes a sodium ion- and chloride ion-dependent high-affinity transporter that mediates choline uptake for acetylcholine synthesis in cholinergic neurons. The protein transports choline from the extracellular space into presynaptic terminals for synthesis into acetylcholine. Increased choline uptake results from increased density of this protein in synaptosomal plasma membranes in response to depolarization of cholinergic terminals. Dysfunction of cholinergic signaling has been implicated in various disorders including depression, attention-deficit disorder, and schizophrenia. An allelic variant of this gene is associated with autosomal dominant distal hereditary motor neuronopathy type VIIA. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]

ACMG classification

Verdict is Benign. Variant got -14 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BP6: Variant 2-107987811-A-G is Benign according to our data. Variant chr2-107987811-A-G is described in ClinVar as [Benign]. Clinvar id is 1227315.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.108 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
SLC5A7	NM_021815.5	c.-51-294A>G		intron_variant		ENST00000264047.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
SLC5A7	ENST00000264047.3	c.-51-294A>G		intron_variant		1	NM_021815.5	P1
SLC5A7	ENST00000409059.5	c.-48-297A>G		intron_variant		1		P1

Frequencies

GnomAD3 genomes AF: 0.0421 AC: 6400 AN: 152176 Hom.: 166 Cov.: 33

Gnomad AFR AF: 0.0362

Gnomad AMI AF: 0.0987

Gnomad AMR AF: 0.0417

Gnomad ASJ AF: 0.0461

Gnomad EAS AF: 0.0327

Gnomad SAS AF: 0.117

Gnomad FIN AF: 0.0527

Gnomad MID AF: 0.0506

Gnomad NFE AF: 0.0383

Gnomad OTH AF: 0.0473

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

GnomAD4 genome AF: 0.0420 AC: 6389 AN: 152294 Hom.: 166 Cov.: 33 AF XY: 0.0443 AC XY: 3295 AN XY: 74460

Gnomad4 AFR AF: 0.0361

Gnomad4 AMR AF: 0.0416

Gnomad4 ASJ AF: 0.0461

Gnomad4 EAS AF: 0.0324

Gnomad4 SAS AF: 0.116

Gnomad4 FIN AF: 0.0527

Gnomad4 NFE AF: 0.0383

Gnomad4 OTH AF: 0.0478

Alfa AF: 0.0411 Hom.: 33

Bravo AF: 0.0373

Asia WGS AF: 0.0820 AC: 283 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

Oct 17, 2018

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
CADD	Benign	14
DANN	Benign	0.37

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.12		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: rs17036563; hg19: chr2-108604267;