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Links from Gene

Items: 1 to 100 of 761

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FANCL, VRK2
(S320G +2 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
FANCL, VRK2
(E458A +2 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
FANCL, VRK2
(T355I +2 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
FANCL, VRK2
(I441V +2 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
FANCL, VRK2
(K325Q +2 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
FANCL
(D296N +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FANCL
(A6V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FANCL
Single nucleotide variant
(splice acceptor variant)
Neoplasm
OLikely oncogenic
FANCL, VRK2
Duplication
Fanconi anemia
GUncertain significance
FANCL, VRK2
Deletion
Fanconi anemia
GLikely pathogenic
FANCL
Deletion
Fanconi anemia
GPathogenic
FANCL, VRK2
Deletion
Fanconi anemia
GPathogenic
FANCL
Deletion
Fanconi anemia
GPathogenic
FANCL
Deletion
Fanconi anemia
GPathogenic
FANCL
Deletion
Fanconi anemia
GPathogenic
FANCL
Deletion
Fanconi anemia
GPathogenic
FANCL
(F356fs +3 more)
Duplication
(frameshift variant)
Fanconi anemia complementation group L
GLikely pathogenic
FANCL
Single nucleotide variant
(splice donor variant)
Fanconi anemia complementation group L
GLikely pathogenic
FANCL
(L114fs)
Duplication
(frameshift variant)
Fanconi anemia complementation group L
GLikely pathogenic
FANCL
(H148fs)
Deletion
(frameshift variant)
Fanconi anemia complementation group L
GLikely pathogenic
FANCL
(E340fs +3 more)
Insertion
(frameshift variant)
Fanconi anemia complementation group L
GLikely pathogenic
FANCL, VRK2
(L482F +2 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
FANCL, VRK2
(E382V +2 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
FANCL
(Q342E +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FANCL
(Q302E +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FANCL
(R10S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FANCL
Copy number loss
not specified
GUncertain significance
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
(L16R)
Single nucleotide variant
(missense variant)
Fanconi anemia
GUncertain significance
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
(E221* +3 more)
Single nucleotide variant
(nonsense)
Fanconi anemia
GPathogenic
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
(E5fs)
Deletion
(frameshift variant)
Fanconi anemia
+1 more
GPathogenic/Likely pathogenic
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
Duplication
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GUncertain significance
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
(K213N +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
FANCL
(T246A +3 more)
Single nucleotide variant
(missense variant)
Fanconi anemia
GUncertain significance
FANCL
(L46V)
Single nucleotide variant
(missense variant)
Fanconi anemia
GUncertain significance
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
Duplication
(intron variant)
Fanconi anemia
GBenign
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(splice donor variant)
Fanconi anemia
GLikely pathogenic
FANCL
(Q11*)
Single nucleotide variant
(nonsense)
Fanconi anemia
GPathogenic
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
(M224I +3 more)
Single nucleotide variant
(missense variant)
Fanconi anemia
GUncertain significance
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GUncertain significance
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
(V127fs)
Deletion
(frameshift variant)
Fanconi anemia complementation group L
+1 more
GPathogenic/Likely pathogenic
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
(D340V +3 more)
Single nucleotide variant
(missense variant)
Fanconi anemia
GUncertain significance
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GUncertain significance
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
(S21*)
Single nucleotide variant
(nonsense)
Fanconi anemia
GPathogenic
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(splice donor variant)
Fanconi anemia
GLikely pathogenic
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
(Q109*)
Single nucleotide variant
(nonsense)
Fanconi anemia
GPathogenic
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(splice donor variant)
Fanconi anemia
GLikely pathogenic
FANCL
Single nucleotide variant
(intron variant +1 more)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(intron variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
FANCL
Single nucleotide variant
(splice donor variant)
Fanconi anemia
GLikely pathogenic
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia
GLikely benign
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