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Links from Gene

Items: 1 to 100 of 1746

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
BUB1B
(E307G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(E305K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(P301A)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(M300V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
BUB1B
(E286D)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(D280N)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(D276V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(S270R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(G257R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(N255K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(G246A)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(R244P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(A240T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
BUB1B
(F217V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
BUB1B
(E212G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(Q197E)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(S191P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(R188S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(E166Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(E166K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(S16Y)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
BUB1B
(V149I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
BUB1B
(P135S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(N133D)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(G111R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B, BUB1B-PAK6
(G1045E)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
BUB1B, BUB1B-PAK6
(S1043C)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
BUB1B, BUB1B-PAK6
(T1042I)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GLikely benign
BUB1B, BUB1B-PAK6
Single nucleotide variant
(synonymous variant +1 more)
Inborn genetic diseases
GLikely benign
BUB1B, BUB1B-PAK6
(G1039E)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
BUB1B, BUB1B-PAK6
(V1009G)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
BUB1B, BUB1B-PAK6
(D1005N)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
BUB1B, BUB1B-PAK6
Single nucleotide variant
(synonymous variant +1 more)
Inborn genetic diseases
GLikely benign
BUB1B, BUB1B-PAK6
(A1003T)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
BUB1B, BUB1B-PAK6
(N983D)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
BUB1B
(M98V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B, BUB1B-PAK6
Single nucleotide variant
(synonymous variant +1 more)
Inborn genetic diseases
GLikely benign
BUB1B, BUB1B-PAK6
Single nucleotide variant
(synonymous variant +1 more)
Inborn genetic diseases
GLikely benign
BUB1B, BUB1B-PAK6
(K966N)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
BUB1B, BUB1B-PAK6
(L959S)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
BUB1B, BUB1B-PAK6
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
GLikely benign
BUB1B, BUB1B-PAK6
(L927F)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
GUncertain significance
BUB1B, BUB1B-PAK6
(D899G)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
GUncertain significance
BUB1B, BUB1B-PAK6
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
GLikely benign
BUB1B, BUB1B-PAK6
(P897R)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
GUncertain significance
BUB1B, BUB1B-PAK6
(I894M)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
GUncertain significance
BUB1B
(S884G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
BUB1B
(H880Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(E877D)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(L873P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B, LOC130056830
(G9S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(Y864C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(S83R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(C832Y)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
BUB1B
(F822L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
BUB1B
(H821D)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(F819L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(K812M)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
BUB1B
(D804G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(W803C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(V801I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(S797F)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(R786S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B, LOC130056830
(G8R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(K732Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(T710I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(L709F)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(I703T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
BUB1B
(S694N)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(S691P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(G687R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(S683F)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(D675Y)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
BUB1B
(T658P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
BUB1B
(V646G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(D645E)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(P632L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(E624K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(A61V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(C609W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
(A61T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
BUB1B
(P603S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
BUB1B
(A559T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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