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Items: 41

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PDIA5, PHLDB2
+1344 more
Copy number gain
See cases
GPathogenic
ABHD10, ABI3BP
+431 more
Copy number loss
See cases
GPathogenic
TRAT1, TRMT10C
+638 more
Copy number loss
See cases
GPathogenic
CCDC54-AS1, LOC123002328
+682 more
Copy number loss
Chromosome 3q13.31 deletion syndrome
GPathogenic
ABHD10, ABI3BP
+398 more
Copy number loss
See cases
GPathogenic
LOC115995524, LOC115995525
+2647 more
Copy number gain
See cases
GPathogenic
LOC132088858, LOC132088860
+248 more
Copy number gain
See cases
GPathogenic
ABHD10, ATG3
+186 more
Copy number loss
See cases
GPathogenic
LOC129937247, LOC129937248
+127 more
Copy number loss
See cases
GPathogenic
ATG3, ATP6V1A
+106 more
Copy number loss
See cases
GPathogenic
GAP43, GRAMD1C
+105 more
Copy number loss
See cases
GPathogenic
LOC129937275, LOC129937276
+105 more
Copy number loss
See cases
GLikely pathogenic
ATG3, ATP6V1A
+105 more
Copy number loss
See cases
GPathogenic
ADPRH, ARHGAP31
+191 more
Copy number loss
See cases
GPathogenic
ATG3
(E279A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATG3
(E268D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATG3
(P257A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATG3
(E170K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATG3
(D101E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATG3
(A96T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATG3
(E95G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATG3
(R84W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATG3
(Y66H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATG3
(A65T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATG3
(W53R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATG3, BTLA
+9 more
Copy number gain
not provided
GUncertain significance
ABHD10, ATG3
+31 more
Copy number loss
not provided
GUncertain significance
ABHD10, ATG3
+34 more
Copy number loss
Chromosome 3q13.31 deletion syndrome
GPathogenic
ATG3, BTLA
+4 more
Copy number gain
not provided
GUncertain significance
ABHD10, ATG3
+49 more
Copy number loss
not provided
GPathogenic
ABHD10, ATG3
+51 more
Copy number loss
Chromosome 3q13.31 deletion syndrome
GPathogenic
ATG3, ATP6V1A
+22 more
Copy number loss
not specified
GPathogenic
CD200R1L, CCDC191
+22 more
Copy number gain
not provided
GPathogenic
ATG3, BTLA
+8 more
Copy number gain
not provided
GUncertain significance
ATG3, BTLA
+8 more
Copy number gain
not provided
GUncertain significance
BOC, CCDC191
+22 more
Copy number loss
not provided
GPathogenic
ATP6V1A, TIGIT
+25 more
Copy number loss
not provided
GPathogenic
ABHD10, ATG3
+34 more
Copy number loss
not provided
GPathogenic
HHLA2, HIGD1A
+1054 more
Copy number gain
See cases
GPathogenic
A4GNT, AADAC
+1054 more
Copy number gain
See cases
GPathogenic
ABHD10, ALCAM
+53 more
Copy number loss
See cases
GPathogenic
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