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Links from Gene

Items: 17

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC28A3, SLC28A3-AS1
(A559T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC28A3, SLC28A3-AS1
(G439E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC28A3, SLC28A3-AS1
(A588T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126860659, SLC28A3
(W170G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126860659, SLC28A3
(M148K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC28A3, SLC28A3-AS1
(R551H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC28A3, SLC28A3-AS1
(S386P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC28A3, SLC28A3-AS1
(N518S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC28A3, SLC28A3-AS1
(G543R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC28A3, SLC28A3-AS1
(A467P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126860659, SLC28A3
(L147P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC28A3, SLC28A3-AS1
(V600M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC28A3, SLC28A3-AS1
(R585C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC28A3, SLC28A3-AS1
(C486R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC28A3
Copy number gain
not provided
GLikely benign
SLC28A3, SLC28A3-AS1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
SLC28A3, SLC28A3-AS1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
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