chr1-109689902-A-G

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_StrongBA1

The NM_000561.4(GSTM1):​c.361-369A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. 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 0.088 ( 2516 hom., cov: 12)

Consequence

GSTM1
NM_000561.4 intron

Scores

2

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: 0.596
Variant links:
Genes affected
GSTM1 (HGNC:4632): (glutathione S-transferase mu 1) 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. Null mutations of this class mu gene have been linked with an increase in a number of cancers, likely due to an increased susceptibility to environmental toxins and carcinogens. Multiple protein isoforms are encoded by transcript variants of this gene. [provided by RefSeq, Jul 2008]
GSTM2 (HGNC:4634): (glutathione S-transferase mu 2) 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. [provided by RefSeq, Jul 2008]

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ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -12 ACMG points.

BP4
Computational evidence support a benign effect (BayesDel_noAF=-0.9).
BA1
GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.22 is higher than 0.05.

Transcripts

RefSeq

Gene Transcript HGVSc HGVSp Effect #exon/exons MANE Protein UniProt
GSTM1NM_000561.4 linkuse as main transcriptc.361-369A>G intron_variant ENST00000309851.10 NP_000552.2
GSTM1NM_146421.3 linkuse as main transcriptc.361-369A>G intron_variant NP_666533.1
GSTM1XM_005270782.6 linkuse as main transcriptc.259-369A>G intron_variant XP_005270839.1

Ensembl

Gene Transcript HGVSc HGVSp Effect #exon/exons TSL MANE Protein Appris UniProt
GSTM1ENST00000309851.10 linkuse as main transcriptc.361-369A>G intron_variant 1 NM_000561.4 ENSP00000311469 P1P09488-1

Frequencies

GnomAD3 genomes
AF:
0.0877
AC:
7007
AN:
79942
Hom.:
2507
Cov.:
12
show subpopulations
Gnomad AFR
AF:
0.225
Gnomad AMI
AF:
0.00
Gnomad AMR
AF:
0.0381
Gnomad ASJ
AF:
0.00
Gnomad EAS
AF:
0.00788
Gnomad SAS
AF:
0.106
Gnomad FIN
AF:
0.00
Gnomad MID
AF:
0.0571
Gnomad NFE
AF:
0.00290
Gnomad OTH
AF:
0.0664
We have no GnomAD4 exomes data on this position. Probably position not covered by the project.
GnomAD4 genome
AF:
0.0879
AC:
7034
AN:
80052
Hom.:
2516
Cov.:
12
AF XY:
0.0880
AC XY:
3426
AN XY:
38950
show subpopulations
Gnomad4 AFR
AF:
0.225
Gnomad4 AMR
AF:
0.0380
Gnomad4 ASJ
AF:
0.00
Gnomad4 EAS
AF:
0.00788
Gnomad4 SAS
AF:
0.108
Gnomad4 FIN
AF:
0.00
Gnomad4 NFE
AF:
0.00290
Gnomad4 OTH
AF:
0.0663
Alfa
AF:
0.00707
Hom.:
184
Asia WGS
AF:
0.110
AC:
215
AN:
1912

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name
Calibrated prediction
Score
Prediction
BayesDel_noAF
Benign
-0.90
CADD
Benign
7.1
DANN
Benign
0.67

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

Below is the list of publications found by LitVar. It may be empty.

Other links and lift over

dbSNP: rs4147567; hg19: chr1-110232524; API