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Links from Gene

Items: 36

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PLCXD2
(D73N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PLCXD2
(R241L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PLCXD2
(K229N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PLCXD2
(Y218C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PLCXD2
(F217I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PLCXD2
(R200Q)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
PLCXD2
(R179W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PLCXD2
(A77V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PLCXD2
(S61R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ABHD10, ATG3
+31 more
Copy number loss
not provided
GUncertain significance
PLCXD2
(H172R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC54-AS1, LOC123002328
+682 more
Copy number loss
Chromosome 3q13.31 deletion syndrome
GPathogenic
PLCXD2
(R111H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PLCXD2
(R80H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ABHD10, ATG3
+34 more
Copy number loss
Chromosome 3q13.31 deletion syndrome
GPathogenic
PHLDB2, PLCXD2
Single nucleotide variant
(5 prime UTR variant)
not specified
GLikely benign
PLCXD2
(S148T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PLCXD2
(I16T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PLCXD2
(H173Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PLCXD2
(R179Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PLCXD2
(G136C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PLCXD2
(P69A)
Single nucleotide variant
(missense variant)
not specified
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
ABHD10, ALCAM
+29 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
PDIA5, PHLDB2
+1344 more
Copy number gain
See cases
GPathogenic
ABHD10, ABI3BP
+398 more
Copy number loss
See cases
GPathogenic
ABHD10, ABI3BP
+431 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
TRAT1, TRMT10C
+638 more
Copy number loss
See cases
GPathogenic
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