U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 1 to 100 of 4050

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHEK2
Deletion
Familial cancer of breast
GLikely pathogenic
CHEK2
Deletion
Familial cancer of breast
GPathogenic
CHEK2
Duplication
Familial cancer of breast
GUncertain significance
CHEK2
Duplication
(3 prime UTR variant)
Hereditary breast ovarian cancer syndrome
GUncertain significance
CHEK2
Single nucleotide variant
(3 prime UTR variant)
CHEK2-related cancer predisposition
GUncertain significance
CHEK2
Single nucleotide variant
(3 prime UTR variant)
CHEK2-related cancer predisposition
GUncertain significance
CHEK2
Single nucleotide variant
(3 prime UTR variant)
CHEK2-related cancer predisposition
GUncertain significance
CHEK2
Single nucleotide variant
(3 prime UTR variant)
not specified
GLikely benign
CHEK2
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
+5 more
GConflicting classifications of pathogenicity
CHEK2
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
CHEK2
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
CHEK2
Deletion
Familial cancer of breast
GPathogenic
CHEK2
Deletion
Familial cancer of breast
GPathogenic
CHEK2
Duplication
Familial cancer of breast
GUncertain significance
CHEK2
Deletion
Familial cancer of breast
GPathogenic
CHEK2
Deletion
Familial cancer of breast
GPathogenic
CHEK2
Deletion
Familial cancer of breast
GLikely pathogenic
CHEK2
Duplication
Familial cancer of breast
GUncertain significance
CHEK2
Duplication
Familial cancer of breast
GUncertain significance
CHEK2
Single nucleotide variant
(3 prime UTR variant)
not specified
+2 more
GConflicting classifications of pathogenicity
CHEK2
Duplication
Familial cancer of breast
GUncertain significance
CHEK2
Deletion
Familial cancer of breast
GPathogenic
CHEK2
Deletion
Familial cancer of breast
GPathogenic
CHEK2
Deletion
Familial cancer of breast
GPathogenic
CHEK2
Deletion
Familial cancer of breast
GLikely pathogenic
CHEK2
Single nucleotide variant
(3 prime UTR variant)
not specified
+1 more
GLikely benign
CHEK2
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
CHEK2
Duplication
(3 prime UTR variant)
not provided
+2 more
GConflicting classifications of pathogenicity
CHEK2
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
GLikely benign
CHEK2
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
CHEK2
Duplication
Familial cancer of breast
GUncertain significance
CHEK2
Single nucleotide variant
(stop lost)
Familial cancer of breast
GUncertain significance
CHEK2
Single nucleotide variant
(stop lost)
Familial cancer of breast
+1 more
GUncertain significance
CHEK2
Single nucleotide variant
(stop lost)
Familial cancer of breast
GUncertain significance
CHEK2
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
GLikely benign
CHEK2
(L476* +4 more)
Single nucleotide variant
(nonsense)
Familial cancer of breast
GUncertain significance
CHEK2
(L586S +4 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
CHEK2
Duplication
(inframe_insertion)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CHEK2
(L322V +4 more)
Single nucleotide variant
(missense variant)
Familial cancer of breast
GUncertain significance
CHEK2
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
GLikely benign
CHEK2
(V321A +4 more)
Single nucleotide variant
(missense variant)
Familial cancer of breast
GUncertain significance
CHEK2
(V321M +4 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CHEK2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
CHEK2
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+2 more
GLikely benign
CHEK2
(A512V +4 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
CHEK2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
GLikely benign
CHEK2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
CHEK2
(A540V +4 more)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+1 more
GUncertain significance
CHEK2
(A319S +4 more)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+2 more
GUncertain significance
CHEK2
(A540T +4 more)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+1 more
GUncertain significance
CHEK2
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
GLikely benign
CHEK2
(C539F +4 more)
Single nucleotide variant
(missense variant)
Familial cancer of breast
GUncertain significance
CHEK2
(C539Y +4 more)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+1 more
GUncertain significance
CHEK2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
GLikely benign
CHEK2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
GLikely benign
CHEK2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
CHEK2
(V471L +4 more)
Single nucleotide variant
(missense variant)
Familial cancer of breast
GUncertain significance
CHEK2
(V538M +4 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
CHEK2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
CHEK2
(A470fs +4 more)
Deletion
(frameshift variant)
Familial cancer of breast
GUncertain significance
CHEK2
(A470D +4 more)
Single nucleotide variant
(missense variant)
Familial cancer of breast
GUncertain significance
CHEK2
(A537V +4 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
CHEK2
(A537T +4 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CHEK2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
GLikely benign
CHEK2
(P507L +4 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
CHEK2
(P536R +4 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
CHEK2
(P315fs +4 more)
Deletion
(frameshift variant)
Familial cancer of breast
GUncertain significance
CHEK2
(P507S +4 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
CHEK2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
GLikely benign
CHEK2
(R535H +4 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
CHEK2
(P536fs +4 more)
Duplication
(frameshift variant)
Familial cancer of breast
GUncertain significance
CHEK2
(R535C +4 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
CHEK2
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+1 more
GLikely benign
CHEK2
(K313fs +4 more)
Deletion
(frameshift variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
CHEK2
(K313Q +4 more)
Single nucleotide variant
(missense variant)
Familial cancer of breast
GUncertain significance
CHEK2
(K534E +4 more)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+1 more
GUncertain significance
CHEK2
(T312I +4 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CHEK2
(T466fs +4 more)
Deletion
(frameshift variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
CHEK2
(T533R +4 more)
Single nucleotide variant
(missense variant)
Familial cancer of breast
GUncertain significance
CHEK2
(T533S +4 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
CHEK2
(T533A +4 more)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+4 more
GConflicting classifications of pathogenicity
CHEK2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
GLikely benign
CHEK2
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
GLikely benign
CHEK2
(T312fs +4 more)
Deletion
(frameshift variant)
Familial cancer of breast
+2 more
GUncertain significance
CHEK2
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+4 more
GConflicting classifications of pathogenicity
CHEK2
(E531G +4 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CHEK2
(E531K +4 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
CHEK2
(E531* +4 more)
Single nucleotide variant
(nonsense)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
CHEK2
(E531Q +4 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
CHEK2
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
GLikely benign
CHEK2
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GLikely benign
CHEK2
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GBenign/Likely benign
CHEK2
(A309fs +4 more)
Insertion
(frameshift variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
CHEK2
(A573V +4 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
CHEK2
(A530T +4 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
CHEK2
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
GLikely benign
CHEK2
(E305fs +4 more)
Deletion
(frameshift variant)
Familial cancer of breast
GUncertain significance
CHEK2
(G529D +4 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
CHEK2
(G308S +4 more)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+1 more
GUncertain significance
CHEK2
Duplication
(inframe_insertion)
Hereditary cancer-predisposing syndrome
GUncertain significance
Format
Items per page
Sort by
Choose Destination