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: 52

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DIS3
Single nucleotide variant
(stop lost)
not specified
GLikely benign
DIS3
(L956F +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(D817G +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(V898A +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(V900A +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(G709E +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(Y821C +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(I683V +3 more)
Single nucleotide variant
(missense variant)
not specified
GBenign
DIS3
(I633T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(I749F +3 more)
Single nucleotide variant
(missense variant)
Multiple myeloma
GLikely pathogenic
DIS3
(Q627R +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(R623S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(R746C +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
Single nucleotide variant
(synonymous variant)
not specified
GUncertain significance
DIS3
(A563V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(N498D +3 more)
Single nucleotide variant
(missense variant)
DIS3-related disorder
GLikely benign
DIS3
(R476Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(S471P +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(M602I +3 more)
Single nucleotide variant
(missense variant)
Perlman syndrome
GUncertain significance
DIS3
(S425F +3 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
DIS3
(M404V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(A356T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(V340A +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
Single nucleotide variant
(intron variant)
not specified
GBenign
DIS3
(K303R +3 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign/Likely benign
DIS3
(R410G +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(G374D +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(I372V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(A239V +3 more)
Single nucleotide variant
(missense variant)
not specified
GBenign
DIS3
(A228P +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(R354L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(D347N +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(R208K +3 more)
Single nucleotide variant
(missense variant)
DIS3-related disorder
GLikely benign
DIS3
Single nucleotide variant
(synonymous variant)
EBV-positive nodal T- and NK-cell lymphoma
GLikely benign
DIS3
(P193L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(K160R +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(A142T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(W102R +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(A130T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(L217F +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(G214A +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(H69Y +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(I103V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DIS3
(I89T)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
DIS3
Single nucleotide variant
(intron variant)
not specified
GUncertain significance
DIS3
(L67M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DIS3
(P55A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DIS3
(P46Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DIS3
(G41R)
Single nucleotide variant
(missense variant +1 more)
DIS3-related disorder
GLikely benign
DIS3
(G40V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DIS3
(K5R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DIS3
(L2R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
Display optionsSort by LocationDownload
Format
Items per page
Sort by
Choose Destination