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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGFR3
(S84L)
Single nucleotide variant
(missense variant +1 more)
Achondroplasia
+9 more
GPathogenic/Likely pathogenic
FGFR3
(R248C)
Single nucleotide variant
(missense variant +1 more)
Epidermal nevus
+31 more
GPathogenic
FGFR3
(S249C)
Single nucleotide variant
(missense variant +1 more)
Connective tissue disorder
+17 more
GPathogenic
OOncogenic
FGFR3
(P250R)
Single nucleotide variant
(missense variant +1 more)
Achondroplasia
+26 more
GPathogenic/Likely pathogenic
FGFR3
(Y373C +1 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+1 more
GPathogenic
FGFR3
(G380R +1 more)
Single nucleotide variant
(missense variant +2 more)
Connective tissue disorder
+18 more
GPathogenic/Likely pathogenic
FGFR3
(N540K +3 more)
Single nucleotide variant
(missense variant +1 more)
Achondroplasia
+18 more
GPathogenic/Likely pathogenic
FGFR3
(K650E +3 more)
Single nucleotide variant
(missense variant +1 more)
Thanatophoric dysplasia type 1
+3 more
GPathogenic
FGFR3
(V784G)
Single nucleotide variant
(stop lost +2 more)
not provided
GPathogenic
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