U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Links from Gene

Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AGPAT2
(G53fs)
Deletion
(frameshift variant)
Congenital generalized lipodystrophy type 1
GLikely pathogenic
AGPAT2
(R51C)
Single nucleotide variant
(missense variant)
Congenital generalized lipodystrophy type 1
GUncertain significance
AGPAT2
(P231R +1 more)
Single nucleotide variant
(missense variant)
Congenital generalized lipodystrophy type 1
GUncertain significance
AGPAT2
(A8T)
Single nucleotide variant
(missense variant)
Congenital generalized lipodystrophy type 1
GUncertain significance
AGPAT2
(K186T)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
AGPAT2
(M252T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AGPAT2
Microsatellite
(inframe_insertion)
not provided
GUncertain significance
AGPAT2
Deletion
Congenital generalized lipodystrophy type 1
GPathogenic
AGPAT2
Single nucleotide variant
(3 prime UTR variant)
not specified
GLikely benign
AGPAT2
(P83fs)
Deletion
(frameshift variant)
Malignant tumor of prostate
GUncertain significance
Format
Items per page
Sort by
Choose Destination