rs1332018

Variant names:

• chr1-109740350-G-T
• rs1332018
• NM_000849.5:c.-63C>A

Your query was ambiguous. Multiple possible variants found:

• chr1-109740350-G-T
• chr1-109740350-G-A

Variant summary

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

The NM_000849.5(GSTM3):​c.-63C>A variant causes a 5 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.6 in 1,456,204 control chromosomes in the GnomAD database, including 267,128 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as (no stars).

• Frequency:
  • Genomes: 𝑓 0.66 (34123 hom., cov: 33)
  • Exomes 𝑓: 0.59 (233005 hom.)
• Consequence: GSTM3 NM_000849.5 5_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.907
• Publications: 73 publications found

Genes affected

GSTM3 (HGNC:4635): (glutathione S-transferase mu 3) Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S-transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S-transferase that belongs to the mu class. The mu class of enzymes functions in the detoxification of electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins and products of oxidative stress, by conjugation with glutathione. The genes encoding the mu class of enzymes are organized in a gene cluster on chromosome 1p13.3 and are known to be highly polymorphic. These genetic variations can change an individual's susceptibility to carcinogens and toxins as well as affect the toxicity and efficacy of certain drugs. Mutations of this class mu gene have been linked with a slight increase in a number of cancers, likely due to exposure with environmental toxins. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]

GSTM5 (HGNC:4637): (glutathione S-transferase mu 5) Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S-transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S-transferase that belongs to the mu class. The mu class of enzymes functions in the detoxification of electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins and products of oxidative stress, by conjugation with glutathione. The genes encoding the mu class of enzymes are organized in a gene cluster on chromosome 1p13.3 and are known to be highly polymorphic. These genetic variations can change an individual's susceptibility to carcinogens and toxins as well as affect the toxicity and efficacy of certain drugs. Diversification of these genes has occurred in regions encoding substrate-binding domains, as well as in tissue expression patterns, to accommodate an increasing number of foreign compounds. [provided by RefSeq, Jul 2008]

ENSG00000241720 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.67).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.821 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_000849.5. 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
	GSTM3	NM_000849.5	MANE Select	c.-63C>A		5_prime_UTR	Exon 2 of 9	NP_000840.2
	GSTM3	NR_024537.2		n.248C>A		non_coding_transcript_exon	Exon 2 of 8

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GSTM3	ENST00000361066.7	TSL:1 MANE Select	c.-63C>A		5_prime_UTR	Exon 2 of 9	ENSP00000354357.2	P21266
	GSTM3	ENST00000256594.7	TSL:1	c.-63C>A		5_prime_UTR	Exon 1 of 8	ENSP00000256594.3	P21266
	GSTM5	ENST00000429410.2	TSL:2	n.82+28002G>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.659 AC: 100187 AN: 151988 Hom.: 34076 Cov.: 33

Gnomad AFR AF: 0.828

Gnomad AMI AF: 0.645

Gnomad AMR AF: 0.626

Gnomad ASJ AF: 0.532

Gnomad EAS AF: 0.843

Gnomad SAS AF: 0.699

Gnomad FIN AF: 0.551

Gnomad MID AF: 0.589

Gnomad NFE AF: 0.572

Gnomad OTH AF: 0.620

GnomAD2 exomes AF: 0.635 AC: 132193 AN: 208154 AF XY: 0.631

Gnomad AFR exome AF: 0.837

Gnomad AMR exome AF: 0.664

Gnomad ASJ exome AF: 0.535

Gnomad EAS exome AF: 0.849

Gnomad FIN exome AF: 0.549

Gnomad NFE exome AF: 0.571

Gnomad OTH exome AF: 0.583

GnomAD4 exome AF: 0.594 AC: 774086 AN: 1304100 Hom.: 233005 Cov.: 18 AF XY: 0.596 AC XY: 389601 AN XY: 653982

African (AFR) AF: 0.839 AC: 24984 AN: 29772

American (AMR) AF: 0.659 AC: 26534 AN: 40270

Ashkenazi Jewish (ASJ) AF: 0.534 AC: 13057 AN: 24462

East Asian (EAS) AF: 0.832 AC: 31502 AN: 37876

South Asian (SAS) AF: 0.694 AC: 56083 AN: 80830

European-Finnish (FIN) AF: 0.548 AC: 28075 AN: 51276

Middle Eastern (MID) AF: 0.575 AC: 3131 AN: 5444

European-Non Finnish (NFE) AF: 0.569 AC: 557344 AN: 979194

Other (OTH) AF: 0.607 AC: 33376 AN: 54976

GnomAD4 genome AF: 0.659 AC: 100290 AN: 152104 Hom.: 34123 Cov.: 33 AF XY: 0.659 AC XY: 48971 AN XY: 74350

African (AFR) AF: 0.828 AC: 34388 AN: 41534

American (AMR) AF: 0.626 AC: 9573 AN: 15294

Ashkenazi Jewish (ASJ) AF: 0.532 AC: 1846 AN: 3470

East Asian (EAS) AF: 0.842 AC: 4328 AN: 5142

South Asian (SAS) AF: 0.698 AC: 3367 AN: 4824

European-Finnish (FIN) AF: 0.551 AC: 5823 AN: 10564

Middle Eastern (MID) AF: 0.595 AC: 175 AN: 294

European-Non Finnish (NFE) AF: 0.572 AC: 38887 AN: 67960

Other (OTH) AF: 0.623 AC: 1317 AN: 2114

Alfa AF: 0.608 Hom.: 46556

Bravo AF: 0.670

Asia WGS AF: 0.741 AC: 2581 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.67
CADD	Benign	4.1
DANN	Benign	0.91
PhyloP100		-0.91
PromoterAI		-0.13	Neutral
Mutation Taster		=300/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.030		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: rs1332018; hg19: chr1-110282972;