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Links from Gene

Items: 69

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADH6, LOC100507053
(L273P)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
ADH6, LOC100507053
(A20T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH6, LOC100507053
(E361K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH6, LOC100507053
(I78T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1A, LOC100507053
+1 more
(T82I)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ADH1A, LOC100507053
+1 more
(S55G)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ADH6, LOC100507053
(N272H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH6, LOC100507053
(I156V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH6, LOC100507053
(D89N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH6, LOC100507053
(V7F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH6, LOC100507053
(V360A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH6, LOC100507053
(A359G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC100507053, ADH4
(P32R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(R318L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(R318C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(V209L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(C201Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(A207V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(A15T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(F146L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(K151T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(V86A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(V67I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(R375Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(F358S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1A, LOC100507053
(P297H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1A, LOC100507053
(V185L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1A, LOC100507053
(N156S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1A, LOC100507053
(R38H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1A, LOC100507053
(P107L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(A72V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH6, LOC100507053
(N352Y)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH1A, LOC100507053
+1 more
(D50E)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ADH4, LOC100507053
(A241T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(L230P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH6, LOC100507053
(R313C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH4, LOC100507053
(H88R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(F235L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(I111T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1A, LOC100507053
(G174R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1A, LOC100507053
(K136T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH6, LOC100507053
(Q234K)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
ADH6, LOC100507053
(H328Y)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH4, LOC100507053
(A62P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH6, LOC100507053
(A281T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH4, LOC100507053
(I298T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(N231S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1A, LOC100507053
(S266T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(V85I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1A, LOC100507053
(M337T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1A, LOC100507053
(T123N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH6, LOC100507053
(A217T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH6, LOC100507053
(I92T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH6, LOC100507053
(F22L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH4, LOC100507053
(L367V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1A, LOC100507053
(V295L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH6, LOC100507053
(G110S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH1A, LOC100507053
(D298G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH6, LOC100507053
(G73R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1A, LOC100507053
(L308P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(K52E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(P21A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(P32L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH6, LOC100507053
(M337T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH4, LOC100507053
(P106R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1A, LOC100507053
+1 more
(G72S)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ADH4, LOC100507053
(E28K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH4, LOC100507053
(A18fs +1 more)
Duplication
(frameshift variant)
CIC-rearranged sarcoma
Gnot provided
ADH1A, LOC100507053
Single nucleotide variant
(intron variant)
not provided
GBenign
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