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Links from Gene

Items: 19

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129933607, ZFP36L2
Single nucleotide variant
(synonymous variant)
ZFP36L2-related disorder
GLikely benign
LOC129933608, ZFP36L2
(C299W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129933607, ZFP36L2
(P375S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129933607, ZFP36L2
(T337N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129933607, ZFP36L2
(A329V)
Single nucleotide variant
(missense variant)
ZFP36L2-related disorder
GBenign
LOC129933607, ZFP36L2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LOC129933607, ZFP36L2
(G402V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129933607, ZFP36L2
(A330V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129933607, ZFP36L2
(R393C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129933607, ZFP36L2
(A387V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129933607, ZFP36L2
(A356V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129933607, ZFP36L2
(A329T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129933607, ZFP36L2
(A348D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129933607, ZFP36L2
(Q396H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129933607, ZFP36L2
(A351S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129933607, ZFP36L2
(A364V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129933607, ZFP36L2
(A377P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129933607, ZFP36L2
(A364T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZFP36L2, LOC129933606
(S476fs)
Duplication
(frameshift variant)
not provided
Gnot provided
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