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Links from Gene

Items: 14

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C3orf38
(S279G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C3orf38
(K267E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARL13B, ARL6
+47 more
Copy number gain
not provided
GLikely pathogenic
C3orf38, CGGBP1
+2 more
Copy number loss
not provided
GUncertain significance
ZNF654, HTR1F
+2 more
Copy number loss
not provided
GUncertain significance
C3orf38, CGGBP1
+2 more
Copy number gain
not provided
GUncertain significance
HHLA2, HIGD1A
+1054 more
Copy number gain
See cases
GPathogenic
A4GNT, AADAC
+1054 more
Copy number gain
See cases
GPathogenic
C3orf38, CADM2
+118 more
Copy number loss
See cases
GPathogenic
C3orf38, CADM2
+124 more
Copy number loss
See cases
GPathogenic
HTD2, HTR1F
+482 more
Copy number loss
See cases
GPathogenic
C3orf38, CGGBP1
+11 more
Copy number gain
See cases
GLikely benign
C3orf38, CADM2
+89 more
Copy number loss
See cases
GLikely pathogenic
C3orf38, CADM2
+54 more
Copy number loss
See cases
GPathogenic
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