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Items: 1 to 100 of 108

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC27A5
Single nucleotide variant
(3 prime UTR variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
SLC27A5-related condition
+1 more
GConflicting classifications of pathogenicity
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
SLC27A5
(M679V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(R673W +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
SLC27A5
(A669G +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
SLC27A5
(V659F +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(R647L +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
SLC27A5
(R647Q +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(V637L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(P626S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(A618T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(K611N +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(E610D +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
SLC27A5-related condition
+1 more
GConflicting classifications of pathogenicity
SLC27A5
(G595fs +1 more)
Deletion
(frameshift variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
SLC27A5
(E566K +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(intron variant)
SLC27A5-related condition
+1 more
GConflicting classifications of pathogenicity
SLC27A5
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
SLC27A5
(R548C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(M539I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(M539T +1 more)
Single nucleotide variant
(missense variant)
SLC27A5-related condition
+2 more
GLikely benign
SLC27A5
(A538T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(R512L +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
SLC27A5
(P504T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(V500L +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
LOC130065230, SLC27A5
(G493E +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
Deletion
(splice donor variant)
not provided
GUncertain significance
SLC27A5
(G490R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
SLC27A5
(L466R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(intron variant)
SLC27A5-related condition
+1 more
GConflicting classifications of pathogenicity
SLC27A5
(G449R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(R447C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
SLC27A5-related condition
+1 more
GConflicting classifications of pathogenicity
SLC27A5
(M439V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(R422H +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SLC27A5
(R412P +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(G410E +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
SLC27A5
(R404C +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SLC27A5
(R399Q +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(intron variant)
SLC27A5-related condition
+1 more
GConflicting classifications of pathogenicity
SLC27A5
(P393S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(R387Q +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
SLC27A5
(G299fs +1 more)
Deletion
(frameshift variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
SLC27A5
(R372W +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(V344I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(T325A +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
SLC27A5
(M315I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC27A5
(V312I +1 more)
Single nucleotide variant
(missense variant)
SLC27A5-related condition
+1 more
GConflicting classifications of pathogenicity
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(intron variant)
SLC27A5-related condition
+1 more
GConflicting classifications of pathogenicity
SLC27A5
(R281H +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
SLC27A5
(H274Y +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC27A5
(L268V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
SLC27A5
(H254Y +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(R248H +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
SLC27A5
(R232Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
SLC27A5
(A214V)
Single nucleotide variant
(missense variant +1 more)
SLC27A5-related condition
+2 more
GBenign/Likely benign
SLC27A5
(R209Q)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
SLC27A5
(L197M)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
SLC27A5
(V185I)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
SLC27A5
(T175I)
Single nucleotide variant
(missense variant +1 more)
SLC27A5-related condition
+2 more
GConflicting classifications of pathogenicity
SLC27A5
Single nucleotide variant
(synonymous variant +1 more)
SLC27A5-related condition
+1 more
GConflicting classifications of pathogenicity
SLC27A5
(A155V)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
SLC27A5
(R151W)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
SLC27A5
(G141S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
SLC27A5
(A126V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(R123Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
SLC27A5
(A119D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(T115A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign
SLC27A5
(P112L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
SLC27A5
(I92F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
SLC27A5
(P88L)
Single nucleotide variant
(missense variant)
not specified
+2 more
GLikely benign
SLC27A5
(R85H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
SLC27A5
(A72T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
SLC27A5
(G57S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC27A5
(R53Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
SLC27A5
(R53W)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign
SLC27A5
(M50T)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign
SLC27A5
(L37R)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign
SLC27A5
(L36F)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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