U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 24

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PCCA
Microsatellite
(intron variant)
Propionic acidemia
+1 more
GBenign
PCCA
(A75P +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
+2 more
GUncertain significance
PCCA
Microsatellite
(intron variant)
Propionic acidemia
+1 more
GBenign
PCCA
Single nucleotide variant
(splice acceptor variant)
not provided
+1 more
GPathogenic/Likely pathogenic
PCCA
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
PCCA
Single nucleotide variant
(synonymous variant +2 more)
Propionic acidemia
+2 more
GBenign
PCCA
(M229K +1 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
PCCA
(L233fs +1 more)
Deletion
(frameshift variant +2 more)
not provided
+1 more
GPathogenic/Likely pathogenic
PCCA
(R268C +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
+2 more
GConflicting classifications of pathogenicity
PCCA
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
PCCA
(R313* +1 more)
Single nucleotide variant
(nonsense +2 more)
not provided
+1 more
GPathogenic
PCCA
(M316R +2 more)
Single nucleotide variant
(missense variant +2 more)
Propionic acidemia
+1 more
GConflicting classifications of pathogenicity
PCCA
(K316* +2 more)
Duplication
(nonsense +1 more)
Propionic acidemia
+1 more
GPathogenic
PCCA
(G379V +2 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
PCCA
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign/Likely benign
PCCA
(I475V +5 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GBenign/Likely benign
PCCA
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign/Likely benign
PCCA
Indel
(nonsense +1 more)
not provided
GPathogenic
PCCA
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
PCCA
Single nucleotide variant
(intron variant)
not provided
GLikely pathogenic
PCCA
(W596* +5 more)
Single nucleotide variant
(nonsense +1 more)
not provided
+1 more
GPathogenic/Likely pathogenic
PCCA
Deletion
(splice donor variant +1 more)
not provided
+1 more
GPathogenic/Likely pathogenic
PCCA
Single nucleotide variant
(splice donor variant)
not provided
GLikely pathogenic
PCCA
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign/Likely benign
Format
Items per page
Sort by
Choose Destination