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Links from Gene

Items: 73

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZNF681
(K283R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(I221V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(K569R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(R30K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(Q25R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(H216R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(N196S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(H188Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(N158K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(F151L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(P135L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(D8Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(H608Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(K588R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(E59K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(V554E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(I53T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(I492V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(A346V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(H388L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(H472Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(N310S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(I274T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(Q461H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(C20W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(K146N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(R166G)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ZNF681
(G159R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(I53F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(A542T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(T466A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(C371Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(K171N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(T389A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(H580Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(C203R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(T361S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(C231Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(G209V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(H328R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(T382I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(K339T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF681
(R306G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF675, ZNF681
+2 more
Copy number gain
not provided
GUncertain significance
ACP7, ACTMAP
+255 more
Copy number gain
Specific learning disability
GPathogenic
ZNF99, ZNF492
+7 more
Copy number gain
See cases
GUncertain significance
ZNF254, ZNF675
+2 more
Copy number gain
not provided
GUncertain significance
ZNF254, ZNF492
+7 more
Copy number gain
not provided
GLikely benign
ZNF675, ZNF681
+2 more
Copy number gain
not provided
GLikely benign
LOC125371498, LOC130064105
+5 more
Deletion
Primary amenorrhea
GLikely benign
PGLYRP1, PGLYRP2
+1364 more
Copy number gain
See cases
GPathogenic
TMC4, TMED1
+1364 more
Copy number gain
See cases
GPathogenic
ZNF675, ZNF681
+1 more
Copy number gain
See cases
GUncertain significance
ZNF254, ZNF681
+1 more
Copy number gain
See cases
GUncertain significance
ZNF675, ZNF681
Copy number loss
See cases
GLikely benign
ATP13A1, BORCS8
+49 more
Complex
Breast ductal adenocarcinoma
GUncertain significance
LOC125371498, LOC130064105
+5 more
Copy number loss
See cases
GUncertain significance
LINC03085, LOC100505851
+14 more
Copy number gain
See cases
GUncertain significance
LOC100505851, LOC125371498
+15 more
Copy number loss
See cases
GBenign
LINC03085, LOC100505851
+15 more
Copy number gain
See cases
GUncertain significance
LINC03085, LOC100505851
+14 more
Copy number gain
See cases
GUncertain significance
LINC03085, LOC100505851
+15 more
Copy number gain
See cases
GUncertain significance
LOC100505851, LOC125371498
+7 more
Copy number gain
See cases
GUncertain significance
LINC03085, LOC100505851
+14 more
Copy number gain
See cases
Gconflicting data from submitters
LOC125371498, LOC130064105
+5 more
Copy number loss
See cases
Gconflicting data from submitters
ABHD8, AKAP8
+574 more
Copy number gain
See cases
GPathogenic
LINC03085, LOC100505851
+14 more
Copy number gain
See cases
GUncertain significance
LOC100505851, LOC125371498
+7 more
Copy number gain
See cases
GLikely benign
LINC03085, LOC100505851
+14 more
Copy number gain
See cases
GUncertain significance
LOC125371498, LOC130064105
+5 more
Copy number loss
See cases
GBenign/Likely benign
ABHD8, ACP5
+2135 more
Copy number gain
See cases
GPathogenic
ABHD8, ADGRE2
+695 more
Copy number gain
See cases
GPathogenic
LOC130064154, LOC130064155
+625 more
Copy number gain
See cases
GPathogenic
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