Project HERA
DICER1 variants
Every DICER1 variant the pipeline has interpreted, classified against the ClinGen expert-panel specification for the gene where one exists.
DICER1 variants
Newest first. Each row opens the full report, criterion by criterion.
Variant
Protein change
Classification
DICER1
NM_177438.3:c.4206+9del
NP_803187.1:p.?
Benign
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DICER1
NM_177438.3:c.4206+9del
NP_803187.1:p.?
Benign
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DICER1
NM_177438.3:c.4206+11_4206+13del
NP_803187.1:p.?
Likely Benign
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DICER1
NM_177438.3:c.4014G>A
NP_803187.1:p.(A1338=)
Benign
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DICER1
NM_177438.3:c.735-23A>G
NP_803187.1:p.?
Likely Benign
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DICER1
NM_177438.2:c.2536A>G
NP_803187.1:p.(I846V)
VUS
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DICER1
NM_177438.2:c.3334A>G
NP_803187.1:p.(N1112D)
Likely Benign
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DICER1
NM_177438.2:c.1282G>C
NP_803187.1:p.(E428Q)
VUS
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DICER1
NM_177438.2:c.1708A>T
NP_803187.1:p.(K570*)
Likely Pathogenic
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DICER1
NM_177438.2:c.1468C>T
NP_803187.1:p.(R490C)
VUS
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DICER1
NM_177438.2:c.5125G>C
NP_803187.1:p.(D1709H)
Likely Pathogenic
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DICER1
NM_177438.2:c.4199A>G
NP_803187.1:p.(D1400G)
Likely Benign
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DICER1
NM_177438.3:c.5437G>C
NP_803187.1:p.(E1813Q)
VUS
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DICER1
NM_177438.3:c.2997T>G
NP_803187.1:p.(L999=)
Benign
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DICER1
NM_177438.3:c.4680G>A
NP_803187.1:p.(A1560=)
Benign
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DICER1
NM_177438.3:c.3033G>A
NP_803187.1:p.(A1011=)
Benign
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