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Links from Gene

Items: 21

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130064661, RELB
(P10T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130064661, RELB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LOC130064661, RELB
(P19R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC130064661, RELB
(A28V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC130064661, RELB
(R16P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130064661, RELB
(R16W)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC130064661, RELB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LOC130064661, RELB
(L35F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC130064661, RELB
(G5E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC130064661, RELB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LOC130064661, RELB
(M1V)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC130064661, RELB
(P19A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC130064661, RELB
(G36R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
LOC130064661, RELB
(P26L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
LOC130064661, RELB
(P27R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC130064661, RELB
(G9E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC130064661, RELB
(P30R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
RELB, LOC130064661
(T14P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC130064661, RELB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LOC130064661, RELB
(P13L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
RELB
(R307*)
Single nucleotide variant
(nonsense)
Immunodeficiency 53
GLikely pathogenic
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