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Links from Gene

Items: 1 to 100 of 261

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COL22A1
(E872V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(L691S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(G1527A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(G684D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(G1054R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
COL22A1
(M567R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(K307N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(Y37H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(E959D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P1158S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(Q1170E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P797T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(S1615C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(C382G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(R306W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(T749M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P1197L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(D607H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P1443Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(R568W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(N338D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(G169D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(G723A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P456R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(G1040S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(R232C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(L1480F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(Q1448H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(G3S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(E799K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(G1123V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(R887H)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
COL22A1
(R1272Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(R951H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(K1328N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MROH1, MROH5
+173 more
Copy number gain
not provided
GPathogenic
COL22A1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
COL22A1
(A1481S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(A509T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(R695Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(Y269H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(K754N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(L39R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(G23S)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
COL22A1
(E186V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(R1039P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(Q1525K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(R355P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(D1206G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(S477P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(A168S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(G596E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(G1043D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
COL22A1
(R1365H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
COL22A1
(D317E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(G24S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(R167L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P1596L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P1581L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P1504S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(W14C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(H1424Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(R140C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(N1353H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P1338T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(A133D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(K1328R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(L1265V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P1188S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(R1173H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(K1149T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P1118S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(L1101P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(R1079Q)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
COL22A1
(R106Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(A103V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P998R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P998S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(S97L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P900L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(D875N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P869H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P782S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(F739I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(R74S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(G735A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P724L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(G717E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P704S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(D686N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(E683Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(A670S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(R58Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(E555V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(S546N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(P541T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(G441V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
COL22A1
(A430T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance

Items: 1 to 100 of 261

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