Home / CDC73 c.237+29_237+32del / gnomAD Canada
gnomAD Canada v1.0 · HostSeq
NM_024529.5:c.237+29_237+32del
NP_078805.3:p.?  ·  CDC73
GRCh38
chr1:193,125,238 TTATC>T
GRCh37
chr1:193094368 TTATC>T
rsID
rs80356645
Type
MIXED · intron variant
Allele type
del · 3 alt
Cohort
HostSeq (10,487 genomes)
Flags
was_split
Allele frequency
7.1793%
1322 / 18,414 alleles
PASS
Allele count
1322
adjusted · raw: 1326
Allele number
18,414
adjusted · raw: 18,422
Allele frequency
7.18e-02
7.1793% MAF
Homozygotes
174
alt hom carriers
grpmax FAF95
4.57e-01
East Asian · AC=652 AN=1,336
FAF95 max
4.57e-01
East Asian
FAF99 max
4.45e-01
East Asian
Cohort size
10,487
whole genomes
Raw vs adjusted allele counts
ACANAFHom
Adjusted
PASS genotypes only
 132218,414 7.18e-02 174
Raw
all genotypes
 1326 18,422 7.20e-02 —
Allele frequency by ancestry
GRCh38 · HostSeq genomes · Canada
Population AC AN AF Hom
African/African American
afr
 7 1,020
0.6863%
 0
Latino/Admixed American
amr
 69 836
8.2536%
 3
Ashkenazi Jewish
asj
 30 832
3.6058%
 1
East Asiangrpmax
eas
 652 1,336
48.8024%
 163
European (Finnish)
fin
 1 8
12.5000%
 0
Middle Eastern
mid
 6 144
4.1667%
 0
European (non-Finnish)
nfe
 379 11,742
3.2277%
 1
Remaining individuals
oth
 93 1,136
8.1866%
 5
South Asian
sas
 85 1,360
6.2500%
 1
Total
 1322 18,414
7.1793%
 174
Population codes are displayed as sourced from gnomAD Canada v1.0 without relabelling. Bar widths scaled relative to the grpmax population (East Asian). Grpmax FAF95 = 4.57e-01.
Filtering allele frequency (FAF)
PopulationFAF 95%FAF 99%
Overall
 6.86e-02 6.73e-02
African/African American
afr
 3.22e-03 2.28e-03
Latino/Admixed American
amr
 6.69e-02 6.12e-02
East Asian
eas
 4.57e-01 4.45e-01
European (non-Finnish)
nfe
 2.96e-02 2.85e-02
South Asian
sas
 5.18e-02 4.78e-02
Sex-stratified allele counts are based on inferred chromosomal sex (XX / XY) from coverage of sex chromosomes in the HostSeq cohort.
XX genotypes
738 / 10,592  ·  6.9675%
PopulationACANAFHom
African/African American
afr
 4 552 0.725% 0
Latino/Admixed American
amr
 31 454 6.828% 0
Ashkenazi Jewish
asj
 14 420 3.333% 1
East Asian
eas
 372 744 50.000% 94
European (Finnish)
fin
 1 8 12.500% 0
Middle Eastern
mid
 2 68 2.941% 0
European (non-Finnish)
nfe
 219 7,110 3.080% 1
Remaining individuals
oth
 52 610 8.525% 4
South Asian
sas
 43 626 6.869% 1
XY genotypes
584 / 7,822  ·  7.4661%
PopulationACANAFHom
African/African American
afr
 3 468 0.641% 0
Latino/Admixed American
amr
 38 382 9.948% 3
Ashkenazi Jewish
asj
 16 412 3.883% 0
East Asian
eas
 280 592 47.297% 69
European (Finnish)
fin
 0 — — 0
Middle Eastern
mid
 4 76 5.263% 0
European (non-Finnish)
nfe
 160 4,632 3.454% 0
Remaining individuals
oth
 41 526 7.795% 1
South Asian
sas
 42 734 5.722% 0
Variant quality scores
MQ
Mapping quality
249.6562
FS
Fisher strand bias · lower = better
0.0
MQRankSum
MQ rank sum test
0.0
SOR
Strand odds ratio
0.6697
ReadPosRankSum
Read position rank sum
-0.032
AS_pab_max
Max posterior allele balance
1.0
RF
Random forest score
0.9503
InbreedingCoeff
Inbreeding coefficient
0.2085
Region flags
LCR (low complexity region) segdup (segmental duplication) monoallelic
Allele balance · alt carriers
Allele balance distribution for alt carriers.
Expected heterozygous AB ≈ 0.5. Values near 0 or 1 may indicate homozygosity or data quality issues.
Read depth distribution (all genotypes)
Read depth distribution across all genotypes.
Genotype quality distribution
Genotype quality distribution across all genotypes.
Strand bias table (SB)
ForwardReverse
Reference
 12711 11192
Alternate
 16041 14464
Genotype quality · alt carriers only
GQ distribution for alt allele carriers.
Alt-carrier GQ distribution. High GQ (≥20) indicates confident heterozygous calls.
Read depth · alt carriers only
Depth distribution for alt allele carriers.
Applied filters
PASS singleton was_split
Age at recruitment for heterozygous carriers observed in the HostSeq cohort. Age data is available only for a subset of participants.
Age distribution · heterozygous carriers
Age distribution for heterozygous carriers.
Carriers below age 30: 210 Carriers above age 80: 28
Age distribution · homozygous carriers
Age distribution for homozygous carriers.
Dataset information
Dataset name
gnomAD Canada v1.0
Cohort
HostSeq
Data type
Whole genome sequencing
Reference genome
GRCh38
Total genomes
10,487
Alleles (this variant)
18,414
Alt allele count
1322
Homozygotes
174
Cross-reference links
gnomAD v4.1 (global) gnomad.broadinstitute.org
gnomAD v2.1 (exome) gnomad.broadinstitute.org
ClinVar — NM_024529.5:c.237+29_237+32del ncbi.nlm.nih.gov
Variant interpretation (LYFE Sciences) Back to full report
Acknowledgements & data use
Required attribution · gnomAD Canada v1.0
About this display
LYFE Sciences is an independent, unfunded variant interpretation tool. This page displays population frequency data from gnomAD Canada v1.0; I did not generate, fund, or contribute to this dataset. All data belongs to the gnomAD Canada project and the HostSeq cohort. I am presenting it in a convenient format alongside variant interpretation.
Data source
All population frequency data on this page originates from gnomAD Canada v1.0, produced from the HostSeq whole-genome sequencing cohort and made publicly available by the BC Genome Sciences Centre (BCGSC). The official gnomAD Canada browser is at gnomad.ca and the BCGSC instance at bcgsc.ca/gnomad. Please cite the original resource if you use this data in research.
Population labels
Population ancestry labels are reproduced exactly as provided by gnomAD Canada and the HostSeq cohort. These labels reflect ancestry inference using gnomAD v4 reference population PCA and are governed by the Indigenous data sovereignty principles of the Silent Genomes Project and the Indigenous Background Variant Library (IBVL).
Key references
1
Yoo S et al. HostSeq: a Canadian whole genome sequencing and clinical data resource. BMC Genom Data. 2023. doi:10.1186/s12863-023-01128-3
2
Chen S*, Francioli LC* et al. A genomic mutational constraint map using variation in 76,156 human genomes. Nature. 625, 92–100 (2024). doi:10.1038/s41586-023-06045-0