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Links from Gene

Items: 1 to 100 of 361

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AK7
Duplication
not provided
GUncertain significance
AK7
(A204V)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
AK7
(S153P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AK7
(S83C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AK7
(R617L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AK7
(C473Y +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
AK7
(E310D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AK7
(Y97H)
Single nucleotide variant
(missense variant)
Spermatogenic failure 27
GUncertain significance
AK7
(Q692H)
Single nucleotide variant
(missense variant +1 more)
AK7-related disorder
GLikely benign
AK7
Single nucleotide variant
(intron variant)
not provided
GLikely benign
AK7
(P555L +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(T96R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(N674K +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
AK7
(A93T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(intron variant)
not provided
GLikely benign
AK7
(S183F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(G393R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
AK7
(V325F +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(T96M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(H583R +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
AK7
(Y687H +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(A93V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(A600E +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(E310D +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(C319* +1 more)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
AK7
Single nucleotide variant
(intron variant)
not provided
GLikely benign
AK7, LOC130056398
(A9P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(splice donor variant)
not provided
GUncertain significance
AK7
(R306T)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
AK7
Single nucleotide variant
(intron variant)
not provided
GLikely benign
AK7
Single nucleotide variant
(intron variant)
not provided
GLikely benign
AK7
(E567D +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(E598* +3 more)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
AK7
(V434M +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
AK7
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
AK7
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
AK7
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
AK7
(R495W +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(intron variant)
not provided
GLikely benign
AK7
(G321V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(V308M +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
AK7
Single nucleotide variant
(intron variant)
not provided
GLikely benign
AK7
Microsatellite
(intron variant)
not provided
GLikely benign
AK7
(R486Q +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
AK7
(R606G +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
AK7
(E663G +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
AK7
(R482G +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
AK7
(Y28N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(G223D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(R557Q +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
AK7
Duplication
(splice donor variant)
not provided
GUncertain significance
AK7
(P88fs)
Insertion
(frameshift variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
AK7, LOC130056398
(E3K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(E476del +1 more)
Microsatellite
(inframe_deletion +1 more)
not provided
GUncertain significance
AK7
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
AK7
(R557W +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(M224V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(L531P +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(E236K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(R436S +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
AK7
Single nucleotide variant
(intron variant)
not provided
GLikely benign
AK7
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
AK7
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
AK7
(V392I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(splice donor variant +1 more)
not provided
GUncertain significance
AK7
Single nucleotide variant
(intron variant)
not provided
GLikely benign
AK7
Single nucleotide variant
(intron variant)
not provided
GLikely benign
AK7
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
AK7
(A608V +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(splice donor variant)
not provided
GUncertain significance
AK7
Duplication
(intron variant)
not provided
GBenign
AK7
(V479F +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
AK7
Deletion
(intron variant)
not provided
GUncertain significance
AK7
(C112G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(intron variant)
not provided
GLikely benign
AK7
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
AK7
(V289G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(intron variant)
not provided
GLikely benign
AK7
(M329T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(D318N +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(E467V +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
(R146*)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
AK7
(M126R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
AK7
(R563W +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AK7
Single nucleotide variant
(intron variant)
not provided
GLikely benign
AK7
Single nucleotide variant
(intron variant)
not provided
GLikely benign
AK7
(V425F +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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