5-132673301-G-GAA
Variant names:
Variant summary
Our verdict is Uncertain significance. The variant received 0 ACMG points: 0P and 0B.
No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.
Frequency
Genomes: 𝑓 0.00016 ( 0 hom., cov: 0)
Consequence
Unknown
Scores
Not classified
Clinical Significance
Not reported in ClinVar
Conservation
PhyloP100: 0.885
Publications
1 publications found
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ACMG classification
Our verdict: Uncertain_significance. The variant received 0 ACMG points.
Variant Effect in Transcripts
RefSeq Transcripts
| Sel. | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
There are no transcript annotations for this variant. | |||||||||
Ensembl Transcripts
| Sel. | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
There are no transcript annotations for this variant. | |||||||||
Frequencies
GnomAD3 genomes 0.000154 AC: 21AN: 136112Hom.: 0 Cov.: 0 show subpopulations
GnomAD3 genomes
AF:
AC:
21
AN:
136112
Hom.:
Cov.:
0
Gnomad AFR
AF:
Gnomad AMI
AF:
Gnomad AMR
AF:
Gnomad ASJ
AF:
Gnomad EAS
AF:
Gnomad SAS
AF:
Gnomad FIN
AF:
Gnomad MID
AF:
Gnomad NFE
AF:
Gnomad OTH
AF:
We have no GnomAD4 exomes data on this position. Probably position not covered by the project.
GnomAD4 genome 0.000162 AC: 22AN: 136122Hom.: 0 Cov.: 0 AF XY: 0.000169 AC XY: 11AN XY: 65252 show subpopulations
GnomAD4 genome
AF:
AC:
22
AN:
136122
Hom.:
Cov.:
0
AF XY:
AC XY:
11
AN XY:
65252
show subpopulations
African (AFR)
AF:
AC:
11
AN:
35046
American (AMR)
AF:
AC:
5
AN:
13764
Ashkenazi Jewish (ASJ)
AF:
AC:
0
AN:
3330
East Asian (EAS)
AF:
AC:
0
AN:
4350
South Asian (SAS)
AF:
AC:
1
AN:
4250
European-Finnish (FIN)
AF:
AC:
3
AN:
7980
Middle Eastern (MID)
AF:
AC:
0
AN:
272
European-Non Finnish (NFE)
AF:
AC:
1
AN:
64362
Other (OTH)
AF:
AC:
1
AN:
1890
Allele Balance Distribution
Red line indicates average allele balance
Average allele balance: 0.432
Heterozygous variant carriers
0
1
2
2
3
4
0.00
0.20
0.40
0.60
0.80
0.95
Allele balance
Age Distribution
Genome Het
Variant carriers
0
2
4
6
8
10
<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:
Hom.:
ClinVar
Not reported inComputational scores
Source:
Name
Calibrated prediction
Score
Prediction
PhyloP100
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at
MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.
Publications
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