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Links from Gene

Items: 1 to 100 of 483

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VAV1
(Q480H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
VAV1
(V214F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
VAV1
(P130S)
Single nucleotide variant
(missense variant)
Neoplasm
OUncertain significance
VAV1
Duplication
not provided
GUncertain significance
VAV1
Duplication
not provided
GUncertain significance
VAV1
Deletion
not provided
GUncertain significance
ACER1, ACSBG2
+65 more
Duplication
not provided
GUncertain significance
VAV1
(D690N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
VAV1
(G565S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
VAV1
(M438V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
VAV1
(R516Q +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
(V237I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
(E559K +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
(T24I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
(S651G +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
(G286R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
VAV1
(V699L +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
VAV1
(N687S +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
(L307I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
(R758H +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
(P186T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
(P609T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
(W831C +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
(L619F +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
(N613H +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
VAV1
(R226W +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
(D151N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
VAV1
(Q217K)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
VAV1
(F673L +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
(A641S +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
(P610A +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
(P577L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
(G787S +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
(P223A +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
(F491S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
(I696V +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
VAV1
(T707fs +2 more)
Deletion
(frameshift variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
(K564fs +1 more)
Deletion
(frameshift variant)
not provided
GUncertain significance
VAV1
(E139K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
Deletion
(intron variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
VAV1
(E201K)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
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