rs7133522

Variant names:

• chr12-46208090-G-A
• rs7133522
• NM_030674.4:c.389-469C>T

Variant summary

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

The NM_030674.4(SLC38A1):​c.389-469C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.228 in 152,036 control chromosomes in the GnomAD database, including 5,246 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 0.23 (5246 hom., cov: 32)
• Consequence: SLC38A1 NM_030674.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0270
• Publications: 2 publications found

Genes affected

SLC38A1 (HGNC:13447): (solute carrier family 38 member 1) Amino acid transporters play essential roles in the uptake of nutrients, production of energy, chemical metabolism, detoxification, and neurotransmitter cycling. SLC38A1 is an important transporter of glutamine, an intermediate in the detoxification of ammonia and the production of urea. Glutamine serves as a precursor for the synaptic transmitter, glutamate (Gu et al., 2001 [PubMed 11325958]).[supplied by OMIM, Mar 2008]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.77).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.429 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_030674.4. 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
	SLC38A1	NM_030674.4	MANE Select	c.389-469C>T		intron	N/A	NP_109599.3
	SLC38A1	NM_001278390.1		c.389-469C>T		intron	N/A	NP_001265319.1	F8VX04
	SLC38A1	NM_001077484.2		c.389-469C>T		intron	N/A	NP_001070952.1	Q9H2H9

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SLC38A1	ENST00000398637.10	TSL:1 MANE Select	c.389-469C>T		intron	N/A	ENSP00000381634.4	Q9H2H9
	SLC38A1	ENST00000552197.5	TSL:1	c.389-469C>T		intron	N/A	ENSP00000449756.1	F8VX04
	SLC38A1	ENST00000439706.5	TSL:1	c.389-469C>T		intron	N/A	ENSP00000398142.1	Q9H2H9

Frequencies

GnomAD3 genomes AF: 0.228 AC: 34617 AN: 151918 Hom.: 5224 Cov.: 32

Gnomad AFR AF: 0.433

Gnomad AMI AF: 0.127

Gnomad AMR AF: 0.162

Gnomad ASJ AF: 0.164

Gnomad EAS AF: 0.0750

Gnomad SAS AF: 0.160

Gnomad FIN AF: 0.119

Gnomad MID AF: 0.272

Gnomad NFE AF: 0.156

Gnomad OTH AF: 0.222

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

GnomAD4 genome AF: 0.228 AC: 34691 AN: 152036 Hom.: 5246 Cov.: 32 AF XY: 0.223 AC XY: 16595 AN XY: 74318

African (AFR) AF: 0.434 AC: 17981 AN: 41432

American (AMR) AF: 0.162 AC: 2471 AN: 15278

Ashkenazi Jewish (ASJ) AF: 0.164 AC: 570 AN: 3470

East Asian (EAS) AF: 0.0750 AC: 388 AN: 5174

South Asian (SAS) AF: 0.159 AC: 764 AN: 4814

European-Finnish (FIN) AF: 0.119 AC: 1261 AN: 10564

Middle Eastern (MID) AF: 0.265 AC: 78 AN: 294

European-Non Finnish (NFE) AF: 0.156 AC: 10588 AN: 67986

Other (OTH) AF: 0.224 AC: 474 AN: 2112

Alfa AF: 0.194 Hom.: 596

Bravo AF: 0.239

Asia WGS AF: 0.136 AC: 474 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.77
CADD	Benign	3.9
DANN	Benign	0.79
PhyloP100		-0.027
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: rs7133522; hg19: chr12-46601873;