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Links from Gene

Items: 54

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZNF547
(K163R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(T86S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(R140K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(Y324C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(P141L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(G320R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(L255H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(Y212F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(S134P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(T116M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
ZNF547
(S391F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(Q371P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TRAPPC2B, ZNF547
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ZNF547
(P77S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(M151V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(C298F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(H314R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(A61V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(L222F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(R308K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(A119V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(N200D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(H150R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(K224E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(C223Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(H124Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(R101H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(G107R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(R130T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(V16M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(L248F)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ZNF547
(T91P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(G190A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(I191V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF547
(R37H)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ZNF548, ZNF549
+157 more
Copy number gain
not provided
GPathogenic
VN1R1, AURKC
+14 more
Copy number loss
not provided
GUncertain significance
ZNF805, ZNF17
+11 more
Duplication
not provided
GUncertain significance
PGLYRP1, PGLYRP2
+1364 more
Copy number gain
See cases
GPathogenic
TMC4, TMED1
+1364 more
Copy number gain
See cases
GPathogenic
A1BG, AURKC
+64 more
Copy number gain
See cases
GUncertain significance
A1BG, ACP4
+280 more
Copy number gain
See cases
GPathogenic
A1BG, A1BG-AS1
+547 more
Copy number gain
See cases
GPathogenic
A1BG, A1BG-AS1
+179 more
Copy number gain
See cases
GUncertain significance
OSCAR, PEG3
+782 more
Copy number gain
See cases
GPathogenic
SSC5D, SYT5
+553 more
Copy number gain
See cases
GPathogenic
TMC4, TMEM150B
+537 more
Copy number gain
See cases
GPathogenic
A1BG, A1BG-AS1
+215 more
Copy number gain
See cases
GPathogenic
A1BG, A1BG-AS1
+647 more
Copy number gain
See cases
GPathogenic
LOC130065082, LOC130065083
+806 more
Copy number gain
See cases
GPathogenic
LOC130064903, LOC130064904
+1093 more
Copy number gain
See cases
GPathogenic
LOC130064925, LOC130064926
+1081 more
Copy number gain
See cases
GPathogenic
LOC130065034, LOC130065035
+761 more
Copy number gain
See cases
GPathogenic
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