U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 14

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATM, C11orf65
Single nucleotide variant
(intron variant)
Familial cancer of breast
+6 more
GBenign
ATM, C11orf65
(V2079I)
Single nucleotide variant
(missense variant +1 more)
not specified
+6 more
GBenign/Likely benign
ATM, C11orf65
Deletion
(intron variant)
Ataxia-telangiectasia syndrome
+2 more
GBenign/Likely benign
ATM, C11orf65
(Q2177*)
Single nucleotide variant
(nonsense +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GPathogenic/Likely pathogenic
ATM, C11orf65
Single nucleotide variant
(intron variant)
Ataxia-telangiectasia syndrome
+6 more
GBenign
ATM, C11orf65
(L2307F)
Single nucleotide variant
(missense variant +1 more)
not specified
+4 more
GConflicting classifications of pathogenicity
ATM, C11orf65
(L2330V)
Single nucleotide variant
(missense variant +1 more)
not specified
+6 more
GConflicting classifications of pathogenicity
C11orf65, ATM
Single nucleotide variant
(intron variant)
Ataxia-telangiectasia syndrome
+4 more
GConflicting classifications of pathogenicity
ATM, C11orf65
Single nucleotide variant
(intron variant)
not specified
+3 more
GConflicting classifications of pathogenicity
ATM, C11orf65
Single nucleotide variant
(intron variant)
not specified
+4 more
GBenign/Likely benign
ATM, C11orf65
Single nucleotide variant
(intron variant)
Breast and/or ovarian cancer
+5 more
GBenign/Likely benign
C11orf65, ATM
Single nucleotide variant
(synonymous variant +1 more)
Ataxia-telangiectasia syndrome
+4 more
GBenign/Likely benign
C11orf65, ATM
Single nucleotide variant
(intron variant)
not provided
+5 more
GBenign/Likely benign
ATM, C11orf65
Single nucleotide variant
(splice acceptor variant +1 more)
Ataxia-telangiectasia syndrome
+3 more
GPathogenic/Likely pathogenic
Format
Items per page
Sort by
Choose Destination