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Links from Gene

Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC30A10
(S46Y)
Single nucleotide variant
(5 prime UTR variant +2 more)
Hypermanganesemia with dystonia, polycythemia, and cirrhosis
GUncertain significance
SLC30A10
(T85I)
Single nucleotide variant
(missense variant)
Hypermanganesemia with dystonia, polycythemia, and cirrhosis
GUncertain significance
LOC121725074, SLC30A10
Single nucleotide variant
(intron variant)
not provided
GLikely benign
LOC121725074, SLC30A10
Single nucleotide variant
(intron variant)
not provided
GLikely benign
SLC30A10
Copy number gain
See cases
GLikely benign
SLC30A10
(Q308* +1 more)
Single nucleotide variant
(nonsense +1 more)
Hypermanganesemia with dystonia, polycythemia, and cirrhosis
Gnot provided
SLC30A10
(V193del)
Deletion
(inframe_deletion +1 more)
Hypermanganesemia with dystonia, polycythemia, and cirrhosis
Gnot provided
SLC30A10
(F167S)
Single nucleotide variant
(missense variant +2 more)
Hypermanganesemia with dystonia, polycythemia, and cirrhosis
Gnot provided
SLC30A10
Deletion
(inframe_deletion +2 more)
Hypermanganesemia with dystonia, polycythemia, and cirrhosis
Gnot provided
SLC30A10
(L349P +1 more)
Single nucleotide variant
(missense variant +1 more)
Hypermanganesemia with dystonia, polycythemia, and cirrhosis
Gnot provided
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