U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Links from MedGen

Items: 1 to 100 of 4136

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(T117I)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(L1052V +1 more)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(L1044H +1 more)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(L1044F +1 more)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(R1034G +1 more)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(G109E)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(R1023L +1 more)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(Q1013P +1 more)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(F812L)
Single nucleotide variant
(missense variant)
Dyskeratosis congenita
GLikely benign
TERT
(G106A)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(A1049P +1 more)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(S1045F +1 more)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(L104Q)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(I1036V +1 more)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(L103R)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(L103V)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(T936N +1 more)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(V928M +1 more)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(R899P +1 more)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(Q384H)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(T937S)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
LOC110806263, TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(M922I)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(Q921R)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(P383S)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(D911E)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(E90D)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(C896Y)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(R889G)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(R885G +1 more)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(R381L)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
LOC110806263, TERT
(R83L)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(C828S)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(I820M)
Single nucleotide variant
(missense variant)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(F812S)
Single nucleotide variant
(missense variant)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant)
Dyskeratosis congenita
GLikely benign
TERT
Single nucleotide variant
(synonymous variant)
Dyskeratosis congenita
GLikely benign
LOC110806263, TERT
(R8L)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(S795N)
Single nucleotide variant
(missense variant)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant)
Dyskeratosis congenita
GLikely benign
TERT
(V790D)
Single nucleotide variant
(missense variant)
Dyskeratosis congenita
GUncertain significance
TERT
(A778S)
Single nucleotide variant
(missense variant)
Dyskeratosis congenita
GUncertain significance
TERT
(R774G)
Single nucleotide variant
(missense variant)
Dyskeratosis congenita
GUncertain significance
TERT
(D768G)
Single nucleotide variant
(missense variant)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant)
Dyskeratosis congenita
GLikely benign
TERT
(V763F)
Single nucleotide variant
(missense variant)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(H752D)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(M372I)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(P370H)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(G715A)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(A689D)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(P673S)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(R672L)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(R669L)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(Y667C)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(L654V)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(E652G)
Single nucleotide variant
(non-coding transcript variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(A651V)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(E648Q)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(T644A)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(Y638H)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(N635H)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
LOC110806263, TERT
(A62G)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(S579N)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
LOC110806263, TERT
(V56E)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(M549I)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
Single nucleotide variant
(synonymous variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(S348G)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(E538Q)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(G527R)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GLikely benign
TERT
(P524R)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
TERT
(R515W)
Single nucleotide variant
(missense variant +1 more)
Dyskeratosis congenita
GUncertain significance
Format
Items per page
Sort by
Choose Destination