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Links from Gene

Items: 45

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CIPC
(S249G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(S248R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(N319S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AHSA1, ANGEL1
+20 more
Duplication
not provided
GUncertain significance
CIPC
(V322L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(R301H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(P292A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(S283T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(S247C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(G230S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(L109R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(D62G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(P6R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(S42T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(H396D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCNK, MIR376A1
+353 more
Copy number gain
not provided
GPathogenic
CIPC
(L172P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(L172R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(K186R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(R310W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(E61K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(P397S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(P381A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(P381R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(K101R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(L197F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(H325R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(H314R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(F393L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(D395N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CIPC
(A373S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AREL1, ARF6
+447 more
Copy number gain
See cases
GPathogenic
ADCK1, AHSA1
+35 more
Copy number loss
not provided
GPathogenic
GTF2A1, GZMB
+624 more
Copy number gain
See cases
GPathogenic
ABCD4, ACOT1
+261 more
Copy number gain
See cases
GPathogenic
ADCK1, AHSA1
+27 more
Copy number loss
See cases
GUncertain significance
ABCD4, ABHD12B
+635 more
Copy number gain
See cases
GPathogenic
ACOT6, ACYP1
+59 more
Deletion
Multiple skeletal anomalies
+3 more
GLikely pathogenic
LOC126862060, LOC126862061
+3282 more
Copy number gain
See cases
GPathogenic
ABCD4, ACOT1
+299 more
Copy number loss
See cases
GLikely pathogenic
LOC125048449, LOC125048450
+3277 more
Copy number gain
See cases
GPathogenic
SAMD15, SEL1L
+503 more
Copy number loss
See cases
GPathogenic
LOC130056651, LOC130056652
+1423 more
Copy number gain
See cases
GPathogenic
ADCK1, AHSA1
+155 more
Copy number loss
See cases
GPathogenic
ABCD4, ACYP1
+227 more
Copy number loss
See cases
GPathogenic
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