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Links from Gene

Items: 21

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GSS
Deletion
Glutathione synthetase deficiency with 5-oxoprolinuria
GPathogenic
GSS
(D458G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GSS
(R215S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GSS
(Y66N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GSS
(L56P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GSS
(M271L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GSS
(A161D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GSS
(E402G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GSS
(H447R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GSS
(R273C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GSS
(Q385R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GSS
(R158Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GSS
(G136V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GSS
Insertion
(intron variant)
Schizophrenia
GUncertain significance
GSS
Single nucleotide variant
(intron variant)
not provided
GLikely benign
GSS, LOC130065740
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GLikely benign
GSS
(K306E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GSS
(E281G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GSS
(P358R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GSS
(Y199C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GSS
(A463V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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