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Links from Gene

Items: 30

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGF21, LOC109279247
(S191L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(R154W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(L128I)
Single nucleotide variant
(missense variant)
Neoplasm
OUncertain significance
FGF21, LOC109279247
(P158A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(Y132H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(R105Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(L49I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(R47W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(R45W)
Single nucleotide variant
(missense variant)
Congenital fibrosis of extraocular muscles
GUncertain significance
FGF21, LOC109279247
(P171H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(E62A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(R203Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(F101L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(P88L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(L142V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(L170V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(R124Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(I93V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(D66N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(D155V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC109279247, FGF21
(A182V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(S195N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(A173P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(R163C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(S113W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
(A72T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FGF21, LOC109279247
Single nucleotide variant
(synonymous variant)
not provided
GBenign
FGF21, LOC109279247
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FGF21, LOC109279247
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FGF21, LOC109279247
Single nucleotide variant
(synonymous variant)
not provided
GBenign
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