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Items: 54

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LRRCC1
(A4V)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
LOC130000685, LRRCC1
(C23S)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
LRRCC1
(A47S)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
LRRCC1
(I64V)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GLikely benign
LRRCC1
(G82E)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
LRRCC1
(N84K)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
LRRCC1
(L86V)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
LRRCC1
(L86P)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
LRRCC1
(S95C)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
LRRCC1
(P129L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LRRCC1
(H38R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LRRCC1
(H50Y +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LRRCC1
(I147V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LRRCC1
(D15Y +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LRRCC1
(D80Y +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LRRCC1
(V186F +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LRRCC1
(L188I +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LRRCC1
(L191S +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LRRCC1
(L165S +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LRRCC1
(V269M +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LRRCC1
(T271M +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LRRCC1
(S137Y +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LRRCC1
(D23G +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LRRCC1
(K2R +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(K265N +4 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
LRRCC1
(I411N +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(D150H +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(E163Q +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(A375V +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(L170V +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(A211P +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(K132N +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(A242T +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(I181V +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(L268F +4 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
LRRCC1
(H189R +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(A275V +4 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
LRRCC1
(H476Q +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(R345H +4 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
LRRCC1
(G361A +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(A678V +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(V653I +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(A374E +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(E377G +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(F618L +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(H678Q +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(A681S +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(Q834R +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(E707K +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(V489I +4 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
LRRCC1
(D816E +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
LRRCC1
(T920I +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRCC1
(K926T +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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