X-71324564-GTTTTTTTTT-GTTTTTT
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 0.00057 ( 1 hom., 1 hem., cov: 0)
Consequence
Unknown
Scores
Not classified
Clinical Significance
Not reported in ClinVar
Conservation
PhyloP100: 0.166
Publications
0 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 0.000573 AC: 44AN: 76816Hom.: 1 Cov.: 0 show subpopulations
GnomAD3 genomes
AF:
AC:
44
AN:
76816
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 0.000573 AC: 44AN: 76792Hom.: 1 Cov.: 0 AF XY: 0.0000686 AC XY: 1AN XY: 14572 show subpopulations
GnomAD4 genome
AF:
AC:
44
AN:
76792
Hom.:
Cov.:
0
AF XY:
AC XY:
1
AN XY:
14572
show subpopulations
African (AFR)
AF:
AC:
39
AN:
20624
American (AMR)
AF:
AC:
3
AN:
5925
Ashkenazi Jewish (ASJ)
AF:
AC:
0
AN:
2136
East Asian (EAS)
AF:
AC:
0
AN:
2447
South Asian (SAS)
AF:
AC:
0
AN:
1542
European-Finnish (FIN)
AF:
AC:
1
AN:
1515
Middle Eastern (MID)
AF:
AC:
0
AN:
100
European-Non Finnish (NFE)
AF:
AC:
1
AN:
41066
Other (OTH)
AF:
AC:
0
AN:
915
Allele Balance Distribution
Red line indicates average allele balance
Average allele balance: 0.521
Heterozygous variant carriers
0
3
5
8
10
13
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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