chr10-70170920-C-CTT
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 0.053 ( 311 hom., cov: 0)
Failed GnomAD Quality Control
Consequence
Unknown
Scores
Not classified
Clinical Significance
Not reported in ClinVar
Conservation
PhyloP100: -0.120
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
| Selected | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|
Ensembl Transcripts
| Selected | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|
Frequencies
GnomAD3 genomes 0.0530 AC: 3870AN: 73044Hom.: 311 Cov.: 0 show subpopulations
GnomAD3 genomes
AF:
AC:
3870
AN:
73044
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 0.0530 AC: 3872AN: 73058Hom.: 311 Cov.: 0 AF XY: 0.0504 AC XY: 1621AN XY: 32162 show subpopulations
GnomAD4 genome
Data not reliable, filtered out with message: AS_VQSR
AF:
AC:
3872
AN:
73058
Hom.:
Cov.:
0
AF XY:
AC XY:
1621
AN XY:
32162
show subpopulations
African (AFR)
AF:
AC:
870
AN:
16528
American (AMR)
AF:
AC:
165
AN:
5502
Ashkenazi Jewish (ASJ)
AF:
AC:
91
AN:
2348
East Asian (EAS)
AF:
AC:
104
AN:
2052
South Asian (SAS)
AF:
AC:
41
AN:
1650
European-Finnish (FIN)
AF:
AC:
26
AN:
926
Middle Eastern (MID)
AF:
AC:
1
AN:
72
European-Non Finnish (NFE)
AF:
AC:
2500
AN:
42474
Other (OTH)
AF:
AC:
37
AN:
926
Allele Balance Distribution
Red line indicates average allele balance
Average allele balance: 0.544
Heterozygous variant carriers
0
111
223
334
446
557
0.00
0.20
0.40
0.60
0.80
0.95
Allele balance
Age Distribution
Genome Het
Genome Hom
Variant carriers
0
38
76
114
152
190
<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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