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Links from Gene

Items: 1 to 100 of 148

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NCOA6
(A308V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(M1070V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(P232L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(T984S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(Q1285H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(Q980H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(S1295C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(I1656L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(F489S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(N498D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(L1886M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(T368M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(L1980P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(N1716D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(P831A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSS2, ACTL10
+51 more
Deletion
Glutathione synthetase deficiency with 5-oxoprolinuria
GPathogenic
NCOA6
(Q305R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(A986V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(P1966L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(P1931L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(A1929T)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
NCOA6
(P1923T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(M183T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(G1805D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(P1755A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(S1735G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(L1537P)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
NCOA6
(Q1463K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(P1454S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(P1056S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(P996L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(R936H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(S842L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(P831H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(P738L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(Q733H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(N724S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(Q682P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(G564S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(F519L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(M353V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(G351C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(P1744S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(I1606V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(P666R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(M1162V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(P1810L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(T1206I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(Y13H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(M766T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(A51T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(M737V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(Q906R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(G351S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(Q816L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(S1721G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(T1341A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(H241R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(P1005S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(P1543T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(V2007A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(I2006R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(T1321A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(V1050I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(P1896L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(P576L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(T1291S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(P526L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(A524G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(P666L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(Q267R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(M243V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(N1936I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(M797V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(R969Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(V1571L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(A693V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(R1433W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(S39N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(Q645R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(R1022Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(E942A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(H371Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(P1722L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(N910K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(C1427S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(S1329C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(M1129V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(A1946V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(Q332H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(S1913I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(A521S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(H796P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(M766V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(N735I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(Q530K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NCOA6
(S1123T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(P1699S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(Q1032K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCOA6
(M194I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
Display optionsSort by RelevanceDownload
Format
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