U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 41

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FCRL6
(T52I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(S43P +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(A80P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(T69I +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(V82M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(R85H +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
FCRL6
(C83G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(S84T +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
FCRL6
(L115Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(R138G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
Single nucleotide variant
(synonymous variant)
not provided
GBenign
FCRL6
(R159K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(I167S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FCRL6
(G183W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(V189M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
Single nucleotide variant
(intron variant)
not provided
GLikely benign
FCRL6
(R206H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(L211P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(G214R +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(G221W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(G216E +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(M218T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(S241F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(L262I +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(L262P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(E268G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(N287S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(S293P +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign
FCRL6
(A325V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(R341G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(A336G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(P351S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(P345S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(H375R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(S381N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FCRL6
(V397A +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
FCRL6
(S395C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FCRL6
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
FCRL6
(D428N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FCRL6
(E431D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
Format
Items per page
Sort by
Choose Destination