Project HERA

TET2 variants

Every TET2 variant the pipeline has interpreted, classified against the ClinGen expert-panel specification for the gene where one exists.

21 variants

TET2 variants

Newest first. Each row opens the full report, criterion by criterion.

21 shown
Variant
Protein change
Classification
TET2 NM_001127208.2:c.2193A>G
NP_001120680.1:p.(Q731=)
VUS
View →
TET2 NM_001127208.2:c.2119G>A
NP_001120680.1:p.(A707T)
VUS
View →
TET2 NM_001127208.2:c.4555G>A
NP_001120680.1:p.(G1519R)
VUS
View →
TET2 NM_001127208.2:c.3765C>G
NP_001120680.1:p.(Y1255*)
Likely Pathogenic
View →
TET2 NM_001127208.2:c.822del
NP_001120680.1:p.(N275Ifs*18)
VUS
View →
TET2 NM_001127208.2:c.4354C>T
NP_001120680.1:p.(R1452*)
Likely Pathogenic
View →
TET2 NM_001127208.2:c.4466dup
NP_001120680.1:p.(N1489Kfs*2)
VUS
View →
TET2 NM_001127208.2:c.5920A>C
NP_001120680.1:p.(R1974=)
VUS
View →
TET2 NM_001127208.2:c.5481del
NP_001120680.1:p.(K1827Nfs*6)
Likely Pathogenic
View →
TET2 NM_001127208.2:c.5666C>T
NP_001120680.1:p.(P1889L)
VUS
View →
TET2 NM_001127208.2:c.2152del
NP_001120680.1:p.(L718Ffs*33)
Likely Pathogenic
View →
TET2 NM_001127208.2:c.5651C>A
NP_001120680.1:p.(T1884N)
VUS
View →
TET2 NM_001127208.2:c.4139A>C
NP_001120680.1:p.(H1380P)
Likely Benign
View →
TET2 NM_001127208.2:c.1413C>T
NP_001120680.1:p.(S471=)
VUS
View →
TET2 NM_001127208.2:c.2814_2815del
NP_001120680.1:p.(Q939Dfs*32)
VUS
View →
TET2 NM_001127208.2:c.3796A>T
NP_001120680.1:p.(N1266Y)
VUS
View →
TET2 NM_001127208.2:c.5456T>G
NP_001120680.1:p.(L1819*)
VUS
View →
TET2 NM_001127208.2:c.2926C>T
NP_001120680.1:p.(Q976*)
Likely Pathogenic
View →
TET2 NM_001127208.2:c.3784C>T
NP_001120680.1:p.(R1262W)
VUS
View →
TET2 NM_001127208.2:c.1452T>A
NP_001120680.1:p.(C484*)
Likely Pathogenic
View →
TET2 NM_001127208.2:c.4164_4167del
NP_001120680.1:p.(M1388Ifs*59)
Likely Pathogenic
View →