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: 62

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SNX13
(Q845P +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(M736I +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(N850D +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(R824C +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(G914S +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(F809L +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(I802T +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(R656Q +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(I655F +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(D776N +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(T648A +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(I758T +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(S611N +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(V605F +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(N713T +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(A458V +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
Duplication
(intron variant)
not specified
GBenign
SNX13
(T550A +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(R498C +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(R486C +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(H383L +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(D493E +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(I441M +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(S527F +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(R431C +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(R385K +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(I383V +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(N393S +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(T268I +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(T268S +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(D381G +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(R321H +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
SNX13
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
SNX13
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
SNX13
(C370G +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(F163L +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(A161P +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(N197D +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(I91M +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(I200T +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(L158F +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(L157I +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(R154G +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(R167Q +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(K138R +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SNX13
(D103G +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SNX13
(D183N +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SNX13
(E101K +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SNX13
(A95T +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SNX13
(R170G +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SNX13
Single nucleotide variant
(intron variant)
not provided
GBenign
SNX13
(E79D)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SNX13
(G73E)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SNX13
(S55T)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SNX13
(T53R)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SNX13
(I22V)
Single nucleotide variant
(missense variant +2 more)
not specified
GLikely benign
SNX13
Copy number loss
not provided
GUncertain significance
SNX13
Copy number loss
not provided
GUncertain significance
SNX13
Copy number gain
not provided
GUncertain significance
SNX13
Copy number gain
not provided
GUncertain significance
SNX13
Copy number loss
See cases
GLikely benign
Display optionsSort by LocationDownload
Format
Items per page
Sort by
Choose Destination