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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FAM111B
(F386S +1 more)
Single nucleotide variant
(missense variant)
Hereditary sclerosing poikiloderma with tendon and pulmonary involvement
Gnot provided
FAM111B
(K421del +1 more)
Deletion
(inframe_deletion)
Hereditary sclerosing poikiloderma with tendon and pulmonary involvement
Gnot provided
FAM111B
(Q430P +1 more)
Single nucleotide variant
(missense variant)
Hereditary sclerosing poikiloderma with tendon and pulmonary involvement
Gnot provided
FAM111B
(Y621D +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely pathogenic
FAM111B
(T625N +1 more)
Single nucleotide variant
(missense variant)
Hereditary sclerosing poikiloderma with tendon and pulmonary involvement
Gnot provided
FAM111B
(R627G +1 more)
Single nucleotide variant
(missense variant)
Hereditary sclerosing poikiloderma with tendon and pulmonary involvement
GPathogenic
FAM111B
(R597S +1 more)
Single nucleotide variant
(missense variant)
Hereditary sclerosing poikiloderma with tendon and pulmonary involvement
Gnot provided
FAM111B
(S628N +1 more)
Single nucleotide variant
(missense variant)
Hereditary sclerosing poikiloderma with tendon and pulmonary involvement
GPathogenic
FAM111B
(S598R +1 more)
Single nucleotide variant
(missense variant)
Hereditary sclerosing poikiloderma with tendon and pulmonary involvement
Gnot provided
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