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Items: 52

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NCOA7, NCOA7-AS1
(D2N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA7, NCOA7-AS1
(K11R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA7
(T65S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA7
(H98P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA7
(M105V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA7
(H7R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(V178D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(A199S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(L153V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(A188G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(D300N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA7
(N214K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(P348S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(R367W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(P279L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(T397N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(S283P +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(E401K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(K422E +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(R447Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(N340K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(A481T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(S387L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(I502V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(H503R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(D516N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(E527A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(K427I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(L430I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(K549R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(A452G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(A567V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(D464G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(K580N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(P590L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(S596F +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(D500E +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(G683S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(R582W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(E583Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(D713N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(V637I +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(S648T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(E655K +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(V52I +3 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
NCOA7
(A781V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(A677G +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(R75T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(R99W +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(F786S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(D808N +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA7
(V215L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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