rs2270637

chr8-20179316-C-G

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_003053.4(SLC18A1):c.293G>C(p.Ser98Thr) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.197 in 1,613,998 control chromosomes in the GnomAD database, including 32,335 homozygotes. In-silico tool predicts a benign outcome for this variant. 14/20 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another nucleotide change resulting in same amino acid change has been previously reported as Likely benignin UniProt.

• Frequency:
  • Genomes: 𝑓 0.21 (3378 hom., cov: 33)
  • Exomes 𝑓: 0.20 (28957 hom.)
• Consequence: SLC18A1 NM_003053.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.888

Genes affected

SLC18A1 (HGNC:10934): (solute carrier family 18 member A1) The vesicular monoamine transporter acts to accumulate cytosolic monoamines into vesicles, using the proton gradient maintained across the vesicular membrane. Its proper function is essential to the correct activity of the monoaminergic systems that have been implicated in several human neuropsychiatric disorders. The transporter is a site of action of important drugs, including reserpine and tetrabenazine (Peter et al., 1993 [PubMed 7905859]). See also SLC18A2 (MIM 193001).[supplied by OMIM, Mar 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (MetaRNN=0.0053890646).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.229 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
SLC18A1	NM_003053.4	c.293G>C	p.Ser98Thr	missense_variant	3/16	ENST00000276373.10

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
SLC18A1	ENST00000276373.10	c.293G>C	p.Ser98Thr	missense_variant	3/16	1	NM_003053.4	P1

Frequencies

GnomAD3 genomes AF: 0.205 AC: 31233 AN: 152034 Hom.: 3377 Cov.: 33

Gnomad AFR AF: 0.233

Gnomad AMI AF: 0.174

Gnomad AMR AF: 0.166

Gnomad ASJ AF: 0.155

Gnomad EAS AF: 0.157

Gnomad SAS AF: 0.224

Gnomad FIN AF: 0.279

Gnomad MID AF: 0.130

Gnomad NFE AF: 0.192

Gnomad OTH AF: 0.190

GnomAD3 exomes AF: 0.195 AC: 49121 AN: 251384 Hom.: 5072 AF XY: 0.196 AC XY: 26647 AN XY: 135856

Gnomad AFR exome AF: 0.229

Gnomad AMR exome AF: 0.166

Gnomad ASJ exome AF: 0.162

Gnomad EAS exome AF: 0.136

Gnomad SAS exome AF: 0.219

Gnomad FIN exome AF: 0.278

Gnomad NFE exome AF: 0.190

Gnomad OTH exome AF: 0.189

GnomAD4 exome AF: 0.196 AC: 287216 AN: 1461846 Hom.: 28957 Cov.: 58 AF XY: 0.196 AC XY: 142607 AN XY: 727224

Gnomad4 AFR exome AF: 0.235

Gnomad4 AMR exome AF: 0.165

Gnomad4 ASJ exome AF: 0.158

Gnomad4 EAS exome AF: 0.198

Gnomad4 SAS exome AF: 0.221

Gnomad4 FIN exome AF: 0.274

Gnomad4 NFE exome AF: 0.192

Gnomad4 OTH exome AF: 0.190

GnomAD4 genome AF: 0.205 AC: 31250 AN: 152152 Hom.: 3378 Cov.: 33 AF XY: 0.207 AC XY: 15373 AN XY: 74374

Gnomad4 AFR AF: 0.233

Gnomad4 AMR AF: 0.167

Gnomad4 ASJ AF: 0.155

Gnomad4 EAS AF: 0.157

Gnomad4 SAS AF: 0.224

Gnomad4 FIN AF: 0.279

Gnomad4 NFE AF: 0.192

Gnomad4 OTH AF: 0.188

Alfa AF: 0.190 Hom.: 2151

Bravo AF: 0.194

TwinsUK AF: 0.188 AC: 697

ALSPAC AF: 0.181 AC: 697

ESP6500AA AF: 0.222 AC: 978

ESP6500EA AF: 0.191 AC: 1640

ExAC AF: 0.197 AC: 23951

Asia WGS AF: 0.192 AC: 670 AN: 3478

EpiCase AF: 0.182

EpiControl AF: 0.172

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.071
BayesDel_addAF	Benign	-0.81	T
BayesDel_noAF	Benign	-0.79
Cadd	Benign	0.10
Dann	Benign	0.29
Eigen	Benign	-1.6
Eigen_PC	Benign	-1.6
FATHMM_MKL	Benign	0.12	N
MetaRNN	Benign	0.0054	T;T;T;T;T;T;T
MetaSVM	Benign	-0.92	T
MutationAssessor	Benign	0.13	N;N;N;N;N;N;.
MutationTaster	Benign	1.0	P;P;P;P;P;P
PrimateAI	Benign	0.21	T
PROVEAN	Benign	-0.41	N;N;N;N;N;N;N
REVEL	Benign	0.010
Sift	Benign	0.50	T;T;T;T;T;T;T
Sift4G	Benign	0.60	T;T;T;T;T;T;T
Polyphen		0.033	.;B;B;.;.;.;.
Vest4		0.12
MPC		0.0025
ClinPred		0.0020	T
GERP RS		-5.8
Varity_R		0.044
gMVP		0.49

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs2270637; hg19: chr8-20036827; COSMIC: COSV52347806; COSMIC: COSV52347806;