rs2221198

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_StrongBA1

The NM_007120.3(UGT1A4):​c.868-17057G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.454 in 151,608 control chromosomes in the GnomAD database, including 16,248 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 0.45 ( 16248 hom., cov: 33)

Consequence

UGT1A4
NM_007120.3 intron

Scores

2

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: 0.352

Publications

12 publications found
Variant links:
Genes affected
UGT1A4 (HGNC:12536): (UDP glucuronosyltransferase family 1 member A4) This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. This enzyme has some glucuronidase activity towards bilirubin, although is is more active on amines, steroids, and sapogenins. [provided by RefSeq, Jul 2008]
UGT1A5 (HGNC:12537): (UDP glucuronosyltransferase family 1 member A5) This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. [provided by RefSeq, Jul 2008]
UGT1A3 (HGNC:12535): (UDP glucuronosyltransferase family 1 member A3) This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. Substrates of this enzyme include estrone, 2-hydroxyestrone, and metabolites of benzo alpha-pyrene. [provided by RefSeq, Jul 2008]
UGT1A6 (HGNC:12538): (UDP glucuronosyltransferase family 1 member A6) This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. The enzyme encoded by this gene is active on phenolic and planar compounds. Alternative splicing in the unique 5' end of this gene results in two transcript variants. [provided by RefSeq, Jul 2008]
UGT1A10 (HGNC:12531): (UDP glucuronosyltransferase family 1 member A10) This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. The enzyme encoded by this gene has glucuronidase activity on mycophenolic acid, coumarins, and quinolines. [provided by RefSeq, Jul 2008]
UGT1A8 (HGNC:12540): (UDP glucuronosyltransferase family 1 member A8) This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. The enzyme encoded by this gene has glucuronidase activity with many substrates including coumarins, phenols, anthraquinones, flavones, and some opioids. [provided by RefSeq, Jul 2008]
UGT1A7 (HGNC:12539): (UDP glucuronosyltransferase family 1 member A7) This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. The enzyme encoded by this gene has moderate glucuronidase activity with phenols. [provided by RefSeq, Jul 2008]
UGT1A9 (HGNC:12541): (UDP glucuronosyltransferase family 1 member A9) This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. The enzyme encoded by this gene is active on phenols. [provided by RefSeq, Jul 2008]

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ACMG classification

Classification was made for transcript

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

BP4
Computational evidence support a benign effect (BayesDel_noAF=-0.91).
BA1
GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.564 is higher than 0.05.

Transcripts

RefSeq

Gene Transcript HGVSc HGVSp Effect Exon rank MANE Protein UniProt
UGT1A4NM_007120.3 linkc.868-17057G>A intron_variant Intron 1 of 4 ENST00000373409.8 NP_009051.1
UGT1A5NM_019078.2 linkc.868-17057G>A intron_variant Intron 1 of 4 ENST00000373414.4 NP_061951.1
UGT1A3NM_019093.4 linkc.868-17057G>A intron_variant Intron 1 of 4 ENST00000482026.6 NP_061966.1
UGT1A6NM_001072.4 linkc.862-17057G>A intron_variant Intron 1 of 4 ENST00000305139.11 NP_001063.2
UGT1A10NM_019075.4 linkc.856-17057G>A intron_variant Intron 1 of 4 ENST00000344644.10 NP_061948.1
UGT1A8NM_019076.5 linkc.856-17057G>A intron_variant Intron 1 of 4 ENST00000373450.5 NP_061949.3
UGT1A7NM_019077.3 linkc.856-17057G>A intron_variant Intron 1 of 4 ENST00000373426.4 NP_061950.2
UGT1A9NM_021027.3 linkc.856-17057G>A intron_variant Intron 1 of 4 ENST00000354728.5 NP_066307.1

Ensembl

Gene Transcript HGVSc HGVSp Effect Exon rank TSL MANE Protein Appris UniProt
UGT1A4ENST00000373409.8 linkc.868-17057G>A intron_variant Intron 1 of 4 1 NM_007120.3 ENSP00000362508.4
UGT1A5ENST00000373414.4 linkc.868-17057G>A intron_variant Intron 1 of 4 1 NM_019078.2 ENSP00000362513.3
UGT1A3ENST00000482026.6 linkc.868-17057G>A intron_variant Intron 1 of 4 1 NM_019093.4 ENSP00000418532.1
UGT1A6ENST00000305139.11 linkc.862-17057G>A intron_variant Intron 1 of 4 1 NM_001072.4 ENSP00000303174.6
UGT1A10ENST00000344644.10 linkc.856-17057G>A intron_variant Intron 1 of 4 1 NM_019075.4 ENSP00000343838.5
UGT1A9ENST00000354728.5 linkc.856-17057G>A intron_variant Intron 1 of 4 1 NM_021027.3 ENSP00000346768.4
UGT1A7ENST00000373426.4 linkc.856-17057G>A intron_variant Intron 1 of 4 1 NM_019077.3 ENSP00000362525.3
UGT1A8ENST00000373450.5 linkc.856-17057G>A intron_variant Intron 1 of 4 1 NM_019076.5 ENSP00000362549.4

Frequencies

GnomAD3 genomes
AF:
0.454
AC:
68742
AN:
151488
Hom.:
16226
Cov.:
33
show subpopulations
Gnomad AFR
AF:
0.534
Gnomad AMI
AF:
0.431
Gnomad AMR
AF:
0.441
Gnomad ASJ
AF:
0.487
Gnomad EAS
AF:
0.321
Gnomad SAS
AF:
0.584
Gnomad FIN
AF:
0.471
Gnomad MID
AF:
0.465
Gnomad NFE
AF:
0.405
Gnomad OTH
AF:
0.438
We have no GnomAD4 exomes data on this position. Probably position not covered by the project.
GnomAD4 genome
AF:
0.454
AC:
68794
AN:
151608
Hom.:
16248
Cov.:
33
AF XY:
0.456
AC XY:
33795
AN XY:
74120
show subpopulations
African (AFR)
AF:
0.535
AC:
21919
AN:
40996
American (AMR)
AF:
0.441
AC:
6736
AN:
15290
Ashkenazi Jewish (ASJ)
AF:
0.487
AC:
1691
AN:
3472
East Asian (EAS)
AF:
0.321
AC:
1662
AN:
5178
South Asian (SAS)
AF:
0.582
AC:
2810
AN:
4828
European-Finnish (FIN)
AF:
0.471
AC:
4975
AN:
10572
Middle Eastern (MID)
AF:
0.455
AC:
133
AN:
292
European-Non Finnish (NFE)
AF:
0.405
AC:
27551
AN:
67968
Other (OTH)
AF:
0.440
AC:
930
AN:
2114
Allele Balance Distribution
Red line indicates average allele balance
Average allele balance: 0.502
Heterozygous variant carriers
0
1898
3796
5695
7593
9491
0.00
0.20
0.40
0.60
0.80
0.95
Allele balance

Age Distribution

Genome Het
Genome Hom
Variant carriers
0
636
1272
1908
2544
3180
<30
30-35
35-40
40-45
45-50
50-55
55-60
60-65
65-70
70-75
75-80
>80
Age
Alfa
AF:
0.440
Hom.:
9225
Bravo
AF:
0.452
Asia WGS
AF:
0.444
AC:
1544
AN:
3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name
Calibrated prediction
Score
Prediction
BayesDel_noAF
Benign
-0.91
CADD
Benign
13
DANN
Benign
0.63
PhyloP100
0.35
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

Publications

Other links and lift over

dbSNP: rs2221198; hg19: chr2-234658623; API