U.S. flag

An official website of the United States government

Display optionsSort by LocationDownload
Format
Items per page
Sort by
Choose Destination

Search results

Items: 29

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AGMAT
(A335V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT
(L327P)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
AGMAT
(P324Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT
(L318P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT
(G315D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT
(G268R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT
(R243W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT
(R225Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT
(R218H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT
(R207Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT
(L199I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT
(K198Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT
(D192N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT
(T188M)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
AGMAT
(D136N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT
(L114P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT
(I97T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT
(R95H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT
(G93R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT, LOC129929491
(A74S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT, LOC129929491
(Q65H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT, LOC129929491
(M59V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT, LOC129929491
(S46N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT, LOC129929491
(Q35H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT, LOC129929491
(R34C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT, LOC129929491
(R31C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT, LOC129929491
(P28A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT, LOC129929491
(A10S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGMAT, LOC129929491
(L4R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
Display optionsSort by LocationDownload
Format
Items per page
Sort by
Choose Destination