U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATF3
(S12P)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
ATF3
(V20I)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
ATF3
(S24C)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
ATF3
(P26S)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
ATF3
(K42E)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
ATF3
Single nucleotide variant
(synonymous variant +1 more)
Inborn genetic diseases
GLikely benign
ATF3
(L25F +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ATF3
(A53V +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ATF3
(Q115E +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ATF3
(N168I +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ATF3
(I171T +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
Format
Items per page
Sort by
Choose Destination