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Items: 1 to 100 of 168

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GAPDH, GAU1
+477 more
Deletion
Tumoral calcinosis, hyperphosphatemic, familial, 1
Gnot provided
ACRBP, ADIPOR2
+348 more
Copy number gain
See cases
GPathogenic
ADIPOR2, B4GALNT3
+142 more
Copy number loss
See cases
GPathogenic
ADIPOR2, B4GALNT3
+147 more
Copy number loss
See cases
GPathogenic
TAS2R9, TEAD4
+1258 more
Copy number gain
See cases
GPathogenic
CLEC12A, CLEC12A-AS1
+1258 more
Copy number gain
See cases
GPathogenic
LOC126861410, LOC126861411
+1258 more
Copy number gain
See cases
GPathogenic
ADIPOR2, B4GALNT3
+170 more
Copy number loss
See cases
GPathogenic
ADIPOR2, B4GALNT3
+114 more
Copy number loss
See cases
GPathogenic
A2M, A2M-AS1
+1009 more
Copy number gain
See cases
GPathogenic
ADIPOR2, B4GALNT3
+123 more
Copy number loss
See cases
GPathogenic
LOC130007230, LOC130007231
+1257 more
Copy number gain
See cases
GPathogenic
ADIPOR2, B4GALNT3
+146 more
Copy number loss
See cases
GPathogenic
ACAD10, ACADS
+4836 more
Copy number gain
See cases
GPathogenic
LOC126861494, LOC126861495
+1257 more
Copy number gain
See cases
GPathogenic
ADIPOR2, AKAP3
+218 more
Copy number loss
See cases
GPathogenic
ADIPOR2, B4GALNT3
+126 more
Copy number gain
See cases
GPathogenic
CACNA1C-AS2, CACNA1C-AS4
+1242 more
Copy number gain
See cases
GPathogenic
ADIPOR2, AKAP3
+223 more
Copy number gain
See cases
GPathogenic
A2M, A2M-AS1
+853 more
Copy number gain
See cases
GPathogenic
CACNA1C, CACNA1C-AS1
+42 more
Copy number gain
See cases
GUncertain significance
AKAP3, CACNA1C
+91 more
Copy number loss
See cases
GPathogenic
CACNA1C, CACNA1C-AS1
+39 more
Copy number gain
See cases
GUncertain significance
ITFG2, ITFG2-AS1
(V4L)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ITFG2, ITFG2-AS1
(E13K)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ITFG2, ITFG2-AS1
(I23V)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ITFG2
(V37L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(T41I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(K49R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(N50D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(S53G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(V73E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(D94Y)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(E114G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(R116H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(R116L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(V129I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(D134N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(R141H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(E142G)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ITFG2
(G146A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(L190Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(P192L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(T213A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(G230V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(P235S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(R238Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(V254I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(G267S)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
ITFG2
(E269A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(G319R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(N338D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(F344C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(A359T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(G363S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(V370I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(E383D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(P402L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(D417N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2
(Y430C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ITFG2, NRIP2
(P266L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(G259R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(H258L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(L247V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(E239Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(S229L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(Q216H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(P211S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(R197S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(E195G)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ITFG2, NRIP2
(T177R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(A174P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(R172T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(L142P)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ITFG2, NRIP2
(D141N)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ITFG2, NRIP2
(Q133H)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ITFG2, NRIP2
(P129L)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ITFG2, NRIP2
(R123S)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ITFG2, NRIP2
(R123C)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ITFG2, NRIP2
(S118R)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ITFG2, NRIP2
(R117C)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ITFG2, NRIP2
(S111T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(G109S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(R84G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(L79P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(E70K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(T66M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ITFG2, NRIP2
(P37T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FOXM1, ITFG2
(P691L +14 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FOXM1, ITFG2
(R658H +14 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FOXM1, ITFG2
(N714S +14 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FOXM1, ITFG2
(P691L +14 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FOXM1, ITFG2
(S679L +14 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FOXM1, ITFG2
(P658L +3 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
FOXM1, ITFG2
(P653R +3 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
FOXM1, ITFG2
(P706T +3 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
FOXM1, ITFG2
(L418F +14 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FOXM1, ITFG2
(P633A +14 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FOXM1, ITFG2
(P581A +14 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FOXM1, ITFG2
(P383S +14 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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