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Links from Gene

Items: 92

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HDAC7
(P1002S +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(P821S +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(G612S +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(A394G +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(Q733K +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R327H +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R106W +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(S979L +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HDAC7
(P33A +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R299W +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(P311L +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R241W +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R226Q +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(T21I)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
HDAC7
(P13L)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
HDAC7
(R99Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(P770A +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R661H +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R633W +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R618H +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(E597G +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R563W +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(G538S +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(T542K +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R526G +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(A492V +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R477Q +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ABCD2, ADAMTS20
+34 more
Copy number gain
not specified
GPathogenic
HDAC7
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HDAC7
(L216F +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R939H +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(S540N +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R106G +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(L828V +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(E195A +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(T379A +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(P310H +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(E299K +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R403Q +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(P325R +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(T323I +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(K226N +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(P433L +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(L606V +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(G624R +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R46H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
HDAC7
(R211W +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(N658S +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(P166L +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R270C +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(M72T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(N266S +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(P807R +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R49C +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(H239Q +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(G5R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(S548W +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(D236E +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(V608M +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(N669K +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(E872D +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(P416R +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(T325S +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(G348R +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(E34Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(P54L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(P67H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(R512W +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(P888S +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(E960V +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(A249V +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
HDAC7
(T487A +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(M68L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(M151V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(P821H +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HDAC7
(P20L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
AMIGO2, ANO6
+27 more
Copy number loss
not provided
GPathogenic
ABCD2, ADAMTS20
+72 more
Copy number gain
not specified
GPathogenic
PPHLN1, PRICKLE1
+66 more
Copy number gain
See cases
GLikely pathogenic
HDAC7
(A513G +3 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
HDAC7
(T161M +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
HDAC7
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
HDAC7
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign/Likely benign
HDAC7
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign/Likely benign
HDAC7
Single nucleotide variant
(intron variant)
not provided
GBenign
BICD1, HDAC7
+212 more
Inversion
not specified
GUncertain significance
SLC15A5, SLC16A7
+1006 more
Copy number gain
See cases
GPathogenic
A2M, A2ML1
+1006 more
Copy number gain
See cases
GPathogenic
GALNT8, H2AJ
+1007 more
Copy number gain
See cases
GPathogenic
ABCD2, ADAMTS20
+92 more
Copy number gain
See cases
GPathogenic
ACAD10, ACADS
+4836 more
Copy number gain
See cases
GPathogenic
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