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Links from Gene

Items: 27

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARHGEF11, LRRC71
(D1435N +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(F1467S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(T1492M +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(T1473I +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(T1428N +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(P1450L +3 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ARHGEF11, LRRC71
(P1275T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(Q1137H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(G1291V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(R1450G +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(V1352I +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(P1523L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(R1274W +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(Q1427P +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(S1255N +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(A1485T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(P1319H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(M1464V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(G1454R +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(E1261K +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(W1298C +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(P1275A +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(R1446C +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC71, ARHGEF11
(G1443C +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
(V1243I +3 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ARHGEF11, LRRC71
(R1412H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARHGEF11, LRRC71
Single nucleotide variant
(intron variant)
not provided
GLikely benign
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