U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 33

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXN2
(D10H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FOXN2
(I21F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FOXN2
(A22V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FOXN2
(P42R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FOXN2
(I81V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FOXN2
(S83R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FOXN2
(L85W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FOXN2
(L120P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FOXN2
(N130D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FOXN2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
FOXN2
(N181T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FOXN2
(P191L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FOXN2
(N196S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FOXN2
(Q229R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FOXN2
(R231Q)
Single nucleotide variant
(missense variant +2 more)
not specified
GLikely benign
FOXN2
(M244I)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
FOXN2
(M245I)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
FOXN2
(S250T)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
FOXN2
(A267T)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
FOXN2
(L268S)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
FOXN2
(H279R)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
FOXN2
(L286S)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
FOXN2
(D297G)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
FOXN2
Single nucleotide variant
(synonymous variant +2 more)
not provided
GBenign
FOXN2
(L323V)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
FOXN2
(P334R)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
FOXN2
(V339M)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
FOXN2
(S365G)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
FOXN2
(Q370L)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
FOXN2
(K398R)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
FOXN2
(R411C)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
FOXN2
(R429Q)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
FOXN2
Copy number loss
not provided
GUncertain significance
Format
Items per page
Sort by
Choose Destination