U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 67

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130006206, LOC130006207
+3 more
Deletion
(genic upstream transcript variant)
Somatotroph adenoma
GLikely pathogenic
AIP
Single nucleotide variant
(5 prime UTR variant)
Somatotroph adenoma
Gnot provided
AIP
(M1T)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
AIP
(A2fs)
Insertion
(frameshift variant)
Somatotroph adenoma
Gnot provided
AIP
(R16H)
Single nucleotide variant
(missense variant)
AIP-related condition
+4 more
GConflicting classifications of pathogenicity
AIP
(R22*)
Single nucleotide variant
(nonsense)
Somatotroph adenoma
GPathogenic
AIP
Deletion
(inframe_deletion)
Somatotroph adenoma
GPathogenic
AIP
(E24*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
AIP
Indel
Somatotroph adenoma
GLikely pathogenic
AIP, LOC130006206
+1 more
Deletion
(splice acceptor variant +2 more)
Somatotroph adenoma
GLikely pathogenic
LOC130006206, AIP
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
AIP, LOC130006206
Deletion
(5 prime UTR variant +1 more)
not provided
GUncertain significance
AIP, LOC130006206
(V49M)
Single nucleotide variant
(5 prime UTR variant +1 more)
AIP-related condition
+3 more
GConflicting classifications of pathogenicity
AIP, LOC130006206
(R56S)
Single nucleotide variant
(5 prime UTR variant +1 more)
Somatotroph adenoma
Gnot provided
AIP, LOC130006206
(K58N)
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
AIP, LOC130006206
(R81* +1 more)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
AIP, LOC130006206
(E23fs +1 more)
Deletion
(frameshift variant)
Somatotroph adenoma
Gnot provided
AIP, LOC130006206
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
AIP, LOC130006206
(E84K +1 more)
Single nucleotide variant
(missense variant)
Somatotroph adenoma
Gnot provided
AIP
Single nucleotide variant
(splice acceptor variant)
Somatotroph adenoma
Gnot provided
AIP
(V37fs +1 more)
Deletion
(frameshift variant)
Somatotroph adenoma
Gnot provided
AIP
(K103R +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
AIP
(G117fs +1 more)
Deletion
(frameshift variant)
Somatotroph adenoma
Gnot provided
AIP
(R128H +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
AIP
(H135fs +1 more)
Deletion
(frameshift variant)
Somatotroph adenoma
Gnot provided
AIP
(Q142* +1 more)
Single nucleotide variant
(nonsense)
Somatotroph adenoma
Gnot provided
AIP
Single nucleotide variant
(synonymous variant)
Somatotroph adenoma
Gnot provided
AIP
Single nucleotide variant
(splice donor variant)
Somatotroph adenoma
Gnot provided
AIP
Single nucleotide variant
(intron variant)
Somatotroph adenoma
GLikely benign
AIP
Single nucleotide variant
(splice acceptor variant)
Somatotroph adenoma
Gnot provided
AIP
Single nucleotide variant
(splice acceptor variant)
Somatotroph adenoma
GPathogenic
AIP
(Q164* +1 more)
Single nucleotide variant
(nonsense)
Hereditary cancer-predisposing syndrome
GPathogenic
AIP
(P108fs +1 more)
Deletion
(frameshift variant)
Somatotroph adenoma
Gnot provided
AIP
(E115fs +1 more)
Deletion
(frameshift variant)
Somatotroph adenoma
Gnot provided
AIP
(I182fs +1 more)
Deletion
(frameshift variant)
Somatotroph adenoma
GPathogenic
AIP
(Q184* +1 more)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
AIP
(V195A +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
AIP
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GBenign/Likely benign
AIP
(K201* +1 more)
Single nucleotide variant
(nonsense)
Somatotroph adenoma
Gnot provided
AIP
(E216* +1 more)
Single nucleotide variant
(nonsense)
Somatotroph adenoma
Gnot provided
AIP
(Q217* +1 more)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
AIP
Duplication
(frameshift variant)
Somatotroph adenoma
Gnot provided
AIP
(C238Y +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely pathogenic
AIP
Single nucleotide variant
(synonymous variant)
Somatotroph adenoma
Gnot provided
AIP
(Q239* +1 more)
Single nucleotide variant
(nonsense)
Somatotroph adenoma
Gnot provided
AIP
(K241* +1 more)
Single nucleotide variant
(nonsense)
Somatotroph adenoma
Gnot provided
AIP
(K241E +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
AIP
(Y248del +1 more)
Microsatellite
(inframe_deletion)
Somatotroph adenoma
Gnot provided
AIP
(I257V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AIP
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
AIP
Duplication
(inframe_insertion)
Hereditary cancer-predisposing syndrome
+1 more
GPathogenic
AIP
(Y268C +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
AIP
(Y268* +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GPathogenic
AIP
(Q267*)
Single nucleotide variant
(synonymous variant +1 more)
AIP-related condition
+3 more
GConflicting classifications of pathogenicity
AIP
(R271W +2 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GPathogenic/Likely pathogenic
AIP
(R273fs +2 more)
Duplication
(frameshift variant)
Somatotroph adenoma
GPathogenic
AIP
(A277P +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AIP
(G283fs +2 more)
Deletion
(frameshift variant)
Somatotroph adenoma
Gnot provided
AIP
(A299V +1 more)
Single nucleotide variant
(missense variant +1 more)
AIP-related condition
+3 more
GConflicting classifications of pathogenicity
AIP
(R304* +1 more)
Single nucleotide variant
(nonsense +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GPathogenic
AIP
(R304Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
AIP
(R307fs +1 more)
Duplication
(frameshift variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
AIP
(A322V +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
AIP
Single nucleotide variant
(synonymous variant +1 more)
Somatotroph adenoma
Gnot provided
Somatotroph adenoma
GLikely pathogenic
Somatotroph adenoma
GLikely pathogenic
AIP
Deletion
Somatotroph adenoma
GLikely pathogenic
Format
Items per page
Sort by
Choose Destination