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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COL4A4
(G414C)
Single nucleotide variant
(missense variant)
Alport syndrome
GLikely pathogenic
COL4A5
Single nucleotide variant
(splice donor variant)
Alport syndrome
GPathogenic
COL4A5
(G1185R)
Single nucleotide variant
(missense variant)
Alport syndrome
GLikely pathogenic
COL4A5
(G1235C)
Single nucleotide variant
(missense variant)
Alport syndrome
GLikely pathogenic
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