4-69635828-CA-CAAAAAAAAAAAAAAAAA

Variant summary

Our verdict is Uncertain significance. The variant received 0 ACMG points: 0P and 0B.

The NM_001252275.3(UGT2A1):​c.716-22_716-7dupTTTTTTTTTTTTTTTT variant causes a splice region, intron change involving the alteration of a non-conserved nucleotide. It is difficult to determine the true allele frequency of this variant because it is of type INS_BIG, and the frequency of such variant types in population databases may be underestimated and unreliable. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

Frequency

Genomes: 𝑓 0.076 ( 1305 hom., cov: 0)
Exomes 𝑓: 0.0 ( 0 hom. )
Failed GnomAD Quality Control

Consequence

UGT2A1
NM_001252275.3 splice_region, intron

Scores

Not classified

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: 0.249

Publications

0 publications found
Variant links:
Genes affected
UGT2A2 (HGNC:28183): (UDP glucuronosyltransferase family 2 member A2) The protein encoded by this gene belongs to the UDP-glycosyltransferase family. Members of this protein family play a role in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. The encoded enzyme is expressed in the olfactory neuroepithelium, which lines the posterior nasal cavity and is exposed to a wide range of odorants and airborne toxic compounds. Hence, this protein has been suggested to be involved in clearing lipophilic odorant molecules from the sensory epithelium. This gene shares exon structure with the UDP glucuronosyltransferase 2A1 family member, which encodes N-terminally distinct isoforms. Polymorphisms in this gene may be associated with the loss of taste and smell that is reported by some individuals during SARS-CoV-2 infection. [provided by RefSeq, Jan 2022]
UGT2A1 (HGNC:12542): (UDP glucuronosyltransferase family 2 member A1 complex locus) The protein encoded by this gene belongs to the UDP-glycosyltransferase family. Members of this protein family play a role in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. The encoded enzyme is expressed in the olfactory neuroepithelium, which lines the posterior nasal cavity and is exposed to a wide range of odorants and airborne toxic compounds. Hence, this protein has been suggested to be involved in clearing lipophilic odorant molecules from the sensory epithelium. This gene shares exon structure with the UDP glucuronosyltransferase 2A2 family member, which encodes N-terminally distinct isoforms. Polymorphisms in this gene may be associated with the loss of taste and smell that is reported by some individuals during SARS-CoV-2 infection. [provided by RefSeq, Jan 2022]

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ACMG classification

Classification was made for transcript

Our verdict: Uncertain_significance. The variant received 0 ACMG points.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001252275.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.
GeneTranscriptTagsHGVScHGVSpEffectExon RankProteinUniProt
UGT2A2
NM_001105677.2
MANE Select
c.742+3055_742+3070dupTTTTTTTTTTTTTTTT
intron
N/ANP_001099147.2P0DTE5-1
UGT2A1
NM_001252275.3
MANE Select
c.716-22_716-7dupTTTTTTTTTTTTTTTT
splice_region intron
N/ANP_001239204.2P0DTE4-5
UGT2A1
NM_001389565.1
c.1345+3055_1345+3070dupTTTTTTTTTTTTTTTT
intron
N/ANP_001376494.1

Ensembl Transcripts

Sel.
GeneTranscriptTagsHGVScHGVSpEffectExon RankProteinUniProt
UGT2A2
ENST00000604629.6
TSL:1 MANE Select
c.742+3070_742+3071insTTTTTTTTTTTTTTTT
intron
N/AENSP00000475028.2P0DTE5-1
UGT2A1
ENST00000286604.9
TSL:1 MANE Select
c.716-7_716-6insTTTTTTTTTTTTTTTT
splice_region intron
N/AENSP00000286604.4P0DTE4-5
UGT2A1
ENST00000503640.5
TSL:1
c.715+11101_715+11102insTTTTTTTTTTTTTTTT
intron
N/AENSP00000424478.1P0DTE4-1

Frequencies

GnomAD3 genomes
AF:
0.0764
AC:
3736
AN:
48912
Hom.:
1305
Cov.:
0
show subpopulations
Gnomad AFR
AF:
0.0297
Gnomad AMI
AF:
0.0909
Gnomad AMR
AF:
0.158
Gnomad ASJ
AF:
0.0957
Gnomad EAS
AF:
0.201
Gnomad SAS
AF:
0.101
Gnomad FIN
AF:
0.0459
Gnomad MID
AF:
0.0435
Gnomad NFE
AF:
0.0857
Gnomad OTH
AF:
0.0876
GnomAD4 exome
Data not reliable, filtered out with message: AC0;AS_VQSR
AF:
0.00
AC:
0
AN:
2
Hom.:
0
Cov.:
0
AF XY:
0.00
AC XY:
0
AN XY:
2
African (AFR)
AC:
0
AN:
0
American (AMR)
AC:
0
AN:
0
Ashkenazi Jewish (ASJ)
AC:
0
AN:
0
East Asian (EAS)
AC:
0
AN:
0
South Asian (SAS)
AF:
0.00
AC:
0
AN:
2
European-Finnish (FIN)
AC:
0
AN:
0
Middle Eastern (MID)
AC:
0
AN:
0
European-Non Finnish (NFE)
AC:
0
AN:
0
Other (OTH)
AC:
0
AN:
0
GnomAD4 genome
Data not reliable, filtered out with message: AS_VQSR
AF:
0.0764
AC:
3736
AN:
48920
Hom.:
1305
Cov.:
0
AF XY:
0.0744
AC XY:
1609
AN XY:
21624
show subpopulations
African (AFR)
AF:
0.0297
AC:
444
AN:
14972
American (AMR)
AF:
0.158
AC:
489
AN:
3088
Ashkenazi Jewish (ASJ)
AF:
0.0957
AC:
125
AN:
1306
East Asian (EAS)
AF:
0.201
AC:
292
AN:
1450
South Asian (SAS)
AF:
0.0997
AC:
79
AN:
792
European-Finnish (FIN)
AF:
0.0459
AC:
40
AN:
872
Middle Eastern (MID)
AF:
0.0435
AC:
2
AN:
46
European-Non Finnish (NFE)
AF:
0.0857
AC:
2182
AN:
25458
Other (OTH)
AF:
0.0873
AC:
51
AN:
584
Allele Balance Distribution
Red line indicates average allele balance
Average allele balance: 0.602
Heterozygous variant carriers
0
35
69
104
138
173
0.00
0.20
0.40
0.60
0.80
0.95
Allele balance

Age Distribution

Genome Het
Genome Hom
Variant carriers
0
30
60
90
120
150
<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:
0.00
Hom.:
0

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name
Calibrated prediction
Score
Prediction
PhyloP100
0.25
Mutation Taster
=100/0
polymorphism

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

Other links and lift over

dbSNP: rs1191267919; hg19: chr4-70501546; API