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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COLEC10, LOC101927513
+1 more
(V17L)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
COLEC10, LOC101927513
+1 more
(S25G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
COLEC10, LOC101927513
+1 more
(A36T)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
COLEC10, LOC101927513
+1 more
(E37A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
COLEC10, LOC101927513
+1 more
(T41A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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