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: 93

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAM8
(A820V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(A820T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(A818P +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(G709S +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
ADAM8
(A728G +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(R724P +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(R724H +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
ADAM8
(T778M)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ADAM8
(R768Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
ADAM8
(S758R +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ADAM8
(H699Y)
Single nucleotide variant
(synonymous variant +1 more)
not specified
GLikely benign
ADAM8
(P683L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(G687S)
Single nucleotide variant
(synonymous variant +1 more)
not specified
GLikely benign
ADAM8
(L685F)
Single nucleotide variant
(synonymous variant +1 more)
not specified
GLikely benign
ADAM8
(A679V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(A716V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(R644C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(R698H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(P692H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(R614H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(V591I +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(A650V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(A641V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(P637L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(A633T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(Q562E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(H625Y +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
ADAM8
(V607I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(R601H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(R601C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(W598C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(R551Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(V585M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(Y582C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(A581V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(G579V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(I528V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(I526V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(V512I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(R543W +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ADAM8
(E527K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(A468T +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ADAM8
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ADAM8
(A451T +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
ADAM8
(C418Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(G451S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(A410V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(R433H +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ADAM8
(R394C +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
ADAM8
(R431W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(P387S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(C411Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(G369S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(A360T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(P391L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(R390Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ADAM8
(D339V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(R374G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(M364T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(R322H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(G360S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ADAM8
(R356H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(M293V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(C291R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ADAM8
(A308V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(V249I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(R242Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ADAM8
(N231S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(P225R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(N241H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(V194G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(V233M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(E173K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(V169M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(R161H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(T143M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(D133N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(V130I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(V115M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(R112W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(R84C)
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
ADAM8
(A67S)
Single nucleotide variant
(synonymous variant +1 more)
not specified
GLikely benign
ADAM8
(T96M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(R59*)
Single nucleotide variant
(synonymous variant +1 more)
not specified
GLikely benign
ADAM8
(V60I +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ADAM8
(S58G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM8
(P40L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAM8
(R36H)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
ADAM8
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ADAM8
(A18V)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
ADAM8
(G10R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
Display optionsSort by LocationDownload
Format
Items per page
Sort by
Choose Destination