19-39245644-CATATATATATATATATAT-CATATATATATATATATATATATATATATATAT
Variant names:
Variant summary
Our verdict is Uncertain significance. The variant received 0 ACMG points: 0P and 0B.
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 0.0011 ( 0 hom., cov: 0)
Consequence
Unknown
Scores
Not classified
Clinical Significance
Not reported in ClinVar
Conservation
PhyloP100: 0.240
Publications
1 publications found
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ACMG classification
Our verdict: Uncertain_significance. The variant received 0 ACMG points.
Transcripts
RefSeq
| Gene | Transcript | HGVSc | HGVSp | Effect | Exon rank | MANE | Protein | UniProt |
|---|
Ensembl
| Gene | Transcript | HGVSc | HGVSp | Effect | Exon rank | TSL | MANE | Protein | Appris | UniProt |
|---|
Frequencies
GnomAD3 genomes 0.00108 AC: 148AN: 137570Hom.: 0 Cov.: 0 show subpopulations
GnomAD3 genomes
AF:
AC:
148
AN:
137570
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 0.00108 AC: 148AN: 137622Hom.: 0 Cov.: 0 AF XY: 0.00109 AC XY: 72AN XY: 66032 show subpopulations
GnomAD4 genome
AF:
AC:
148
AN:
137622
Hom.:
Cov.:
0
AF XY:
AC XY:
72
AN XY:
66032
show subpopulations
African (AFR)
AF:
AC:
43
AN:
37270
American (AMR)
AF:
AC:
13
AN:
13346
Ashkenazi Jewish (ASJ)
AF:
AC:
0
AN:
3346
East Asian (EAS)
AF:
AC:
0
AN:
4562
South Asian (SAS)
AF:
AC:
0
AN:
4116
European-Finnish (FIN)
AF:
AC:
1
AN:
7660
Middle Eastern (MID)
AF:
AC:
0
AN:
270
European-Non Finnish (NFE)
AF:
AC:
90
AN:
64284
Other (OTH)
AF:
AC:
1
AN:
1908
Allele Balance Distribution
Red line indicates average allele balance
Average allele balance: 0.418
Heterozygous variant carriers
0
7
14
21
28
35
0.00
0.20
0.40
0.60
0.80
0.95
Allele balance
Age Distribution
Genome Het
Variant carriers
0
4
8
12
16
20
<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
Publications
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