U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AMPD3
Single nucleotide variant
(intron variant)
not specified
GBenign
AMPD3
(R194W +3 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign/Likely benign
AMPD3
Single nucleotide variant
(synonymous variant)
AMPD3-related condition
+2 more
GBenign
AMPD3
(V311L +3 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
AMPD3
(T348M +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
AMPD3
Single nucleotide variant
(intron variant)
not provided
+1 more
GUncertain significance
AMPD3
(S491L +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
AMPD3
Single nucleotide variant
(synonymous variant)
not specified
GBenign
AMPD3
Single nucleotide variant
(synonymous variant)
AMPD3-related condition
+2 more
GBenign
AMPD3
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GUncertain significance
Format
Items per page
Sort by
Choose Destination