Project HERA
TERT variants
Every TERT variant the pipeline has interpreted, classified against the ClinGen expert-panel specification for the gene where one exists.
TERT variants
Newest first. Each row opens the full report, criterion by criterion.
Variant
Protein change
Classification
TERT
NM_198253.2:c.1812A>G
NP_937983.2:p.(A604=)
VUS
View →
TERT
NM_198253.2:c.2283C>T
NP_937983.2:p.(S761=)
VUS
View →
TERT
NM_198253.2:c.2517G>A
NP_937983.2:p.(T839=)
Benign
View →
TERT
NM_198253.2:c.2775C>T
NP_937983.2:p.(H925=)
Likely Benign
View →
TERT
NM_198253.2:c.1234C>T
NP_937983.2:p.(H412Y)
Benign
View →
TERT
NM_198253.2:c.26C>T
NP_937983.2:p.(A9V)
VUS
View →
TERT
NM_198253.2:c.899G>A
NP_937983.2:p.(G300D)
VUS
View →
TERT
NM_198253.2:c.833C>T
NP_937983.2:p.(P278L)
VUS
View →
TERT
NM_198253.2:c.2509C>T
NP_937983.2:p.(L837F)
VUS
View →
TERT
NM_198253.2:c.875C>T
NP_937983.2:p.(T292M)
VUS
View →
TERT
NM_198253.2:c.2765T>A
NP_937983.2:p.(M922K)
—
View →
TERT
NM_198253.2:c.468C>T
NP_937983.2:p.(C156=)
Likely Benign
View →
TERT
NM_198253.2:c.3334C>A
NP_937983.2:p.(L1112M)
VUS
View →
TERT
NM_198253.2:c.2781A>G
NP_937983.2:p.(L927=)
VUS
View →
TERT
NM_198253.2:c.1950+10C>T
NP_937983.2:p.?
Benign
View →
TERT
NM_198253.2:c.2031C>T
NP_937983.2:p.(G677=)
Benign
View →
TERT
NM_198253.2:c.2097C>T
NP_937983.2:p.(A699=)
Benign
View →
TERT
NM_198253.2:c.835G>A
NP_937983.2:p.(A279T)
Benign
View →
TERT
NM_198253.2:c.3184G>A
NP_937983.2:p.(A1062T)
Benign
View →