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Links from Gene

Items: 21

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RNF31
Deletion
not provided
GUncertain significance
LOC121468009, RNF31
(S19N)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC121468009, RNF31
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
LOC121468009, RNF31
(A18T)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC121468009, RNF31
(A20V)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC121468009, RNF31
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
LOC121468009, RNF31
(G3E)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
RNF31
(A235T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC121468009, RNF31
(E7K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC121468009, RNF31
(E15K)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC121468009, RNF31
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
LOC121468009, RNF31
(P2S)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC121468009, RNF31
(R8P)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC121468009, RNF31
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
LOC121468009, RNF31
(A20S)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC121468009, RNF31
(P2L)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
RNF31, LOC121468009
(V12M)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC121468009, RNF31
(E15A)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC121468009, RNF31
(E6K)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC121468009, RNF31
(A20T)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
RNF31
(Y778C +1 more)
Single nucleotide variant
(missense variant)
Short stature
GLikely pathogenic
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