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Items: 65

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KIFC2
(P105L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(V120M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(L141P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(P152S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(P152L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(S158F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(P165S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(P172L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(G182E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(R193K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(Q200H)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
KIFC2
(I202F)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
KIFC2
(G263R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(A275S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(E291V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(T318M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(R324H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(S364L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(P389L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(G391R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(G394R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(G398A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(I410T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KIFC2
(T420R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(S421F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(S426R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(S426N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(G441E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(R447H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(A456V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(I480V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KIFC2
(P498A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(A507V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(S510L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(R513W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(R522W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(P543T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(E545Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(G552V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(P553A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(R586W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(A587S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(T607M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(R615G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(R615H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(A620T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(V626M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(R635L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(Q657H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(G668S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(H676Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(P678A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(P678R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KIFC2
(R718W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIFC2
(R723P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIFC2
(L774R)
Single nucleotide variant
(synonymous variant +1 more)
not specified
GUncertain significance
KIFC2
(P786S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(A788E +1 more)
Single nucleotide variant
(nonsense +1 more)
not specified
GUncertain significance
KIFC2
(A788V)
Single nucleotide variant
(synonymous variant +1 more)
not specified
GUncertain significance
KIFC2
(A815T +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
KIFC2
(P790L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIFC2
(P820S)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
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