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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MAP2K2
(N126D)
Single nucleotide variant
(missense variant)
RASopathy
+1 more
GPathogenic/Likely pathogenic
MAP2K2
(C125S)
Single nucleotide variant
(missense variant)
Melanoma
GLikely pathogenic
MAP2K2
(Q60P)
Single nucleotide variant
(missense variant)
Melanoma
GLikely pathogenic
MAP2K2
(F57L)
Single nucleotide variant
(missense variant)
Pancreatic adenocarcinoma
+3 more
GLikely pathogenic
MAP2K2
(F57V)
Single nucleotide variant
(missense variant)
Cardio-facio-cutaneous syndrome
GPathogenic
MAP2K2
(L46F)
Single nucleotide variant
(missense variant)
Melanoma
GLikely pathogenic
MAP2K2
(V35M)
Single nucleotide variant
(missense variant)
Melanoma
GLikely pathogenic
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