chr22:28699893:C>T Detail (hg38) (CHEK2)

Information

Genome

Assembly Position
hg19 chr22:29,095,881-29,095,881 View the variant detail on this assembly version.
hg38 chr22:28,699,893-28,699,893

HGVS

Type Transcript Protein
RefSeq NM_001257387.1:c.953G>A NP_001244316.1:p.Arg318His
NM_145862.2:c.953G>A NP_665861.1:p.Arg318His
NM_001005735.1:c.1082G>A NP_001005735.1:p.Arg361His
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:[No Data.]
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:<0.001

Prediction

ClinVar

Clinical Significance Uncertain significance
Review star
Show details
Links
Type Database ID Link
Gene MIM 604373 OMIM
HGNC 16627 HGNC
Ensembl ENSG00000183765 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Uncertain significance 2020-08-07 criteria provided, single submitter not specified germline Detail
Uncertain significance 2023-05-05 criteria provided, multiple submitters, no conflicts Hereditary cancer-predisposing syndrome germline Detail
Uncertain significance 2024-01-20 criteria provided, multiple submitters, no conflicts Familial cancer of breast germline unknown Detail
Uncertain significance 2023-08-29 criteria provided, multiple submitters, no conflicts not provided germline Detail
Uncertain significance 2021-07-14 criteria provided, single submitter colorectal cancer,Familial cancer of breast,Malignant tumor of prostate,bone osteosarcoma,Li-Fraumeni syndrome 2 unknown Detail
Uncertain significance 2021-07-14 criteria provided, single submitter colorectal cancer,Familial cancer of breast,Malignant tumor of prostate,bone osteosarcoma,Li-Fraumeni syndrome 2 unknown Detail
Uncertain significance 2021-07-14 criteria provided, single submitter colorectal cancer,Familial cancer of breast,Malignant tumor of prostate,bone osteosarcoma,Li-Fraumeni syndrome 2 unknown Detail
Uncertain significance 2021-07-14 criteria provided, single submitter colorectal cancer,Familial cancer of breast,Malignant tumor of prostate,bone osteosarcoma,Li-Fraumeni syndrome 2 unknown Detail
Uncertain significance 2021-07-14 criteria provided, single submitter colorectal cancer,Familial cancer of breast,Malignant tumor of prostate,bone osteosarcoma,Li-Fraumeni syndrome 2 unknown Detail
Uncertain significance 2022-05-30 criteria provided, single submitter Breast and/or ovarian cancer germline Detail
Uncertain significance 2024-01-30 criteria provided, single submitter CHEK2-related disorder germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.138 Malignant neoplasm of prostate Mutations in CHEK2 associated with prostate cancer risk. UNIPROT 12533788 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_007194.4(CHEK2):c.953G>A (p.Arg318His) AND not specified ClinVar Detail
NM_007194.4(CHEK2):c.953G>A (p.Arg318His) AND Hereditary cancer-predisposing syndrome ClinVar Detail
NM_007194.4(CHEK2):c.953G>A (p.Arg318His) AND Familial cancer of breast ClinVar Detail
NM_007194.4(CHEK2):c.953G>A (p.Arg318His) AND not provided ClinVar Detail
NM_007194.4(CHEK2):c.953G>A (p.Arg318His) AND multiple conditions ClinVar Detail
NM_007194.4(CHEK2):c.953G>A (p.Arg318His) AND multiple conditions ClinVar Detail
NM_007194.4(CHEK2):c.953G>A (p.Arg318His) AND multiple conditions ClinVar Detail
NM_007194.4(CHEK2):c.953G>A (p.Arg318His) AND multiple conditions ClinVar Detail
NM_007194.4(CHEK2):c.953G>A (p.Arg318His) AND multiple conditions ClinVar Detail
NM_007194.4(CHEK2):c.953G>A (p.Arg318His) AND Breast and/or ovarian cancer ClinVar Detail
NM_007194.4(CHEK2):c.953G>A (p.Arg318His) AND CHEK2-related disorder ClinVar Detail
Mutations in CHEK2 associated with prostate cancer risk. DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs143611747 dbSNP
Genome
hg38
Position
chr22:28,699,893-28,699,893
Variant Type
snv
Reference Allele
C
Alternative Allele
T
East Asian Chromosome Counts (ExAC)
8654
East Asian Allele Counts (ExAC)
1
East Asian Heterozygous Counts (ExAC)
1
East Asian Homozygous Counts (ExAC)
0
East Asian Allele Frequency (ExAC)
1.1555350127108852E-4
Chromosome Counts in All Race (ExAC)
121400
Allele Counts in All Race (ExAC)
7
Heterozygous Counts in All Race (ExAC)
7
Homozygous Counts in All Race (ExAC)
0
Allele Frequency in All Race (ExAC)
5.766062602965403E-5
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