Project HERA
NRAS variants
Every NRAS variant the pipeline has interpreted, classified against the ClinGen expert-panel specification for the gene where one exists.
NRAS variants
Newest first. Each row opens the full report, criterion by criterion.
Variant
Protein change
Classification
NRAS
NM_002524.5:c.182A>T
NP_002515.1:p.(Q61L)
VUS
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NRAS
NM_002524.5:c.183A>T
NP_002515.1:p.(Q61H)
Likely Pathogenic
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NRAS
NM_002524.5:c.38G>T
NP_002515.1:p.(G13V)
VUS
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NRAS
NM_002524.5:c.101C>T
NP_002515.1:p.(P34L)
VUS
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NRAS
NM_002524.5:c.182A>G
NP_002515.1:p.(Q61R)
Pathogenic
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NRAS
NM_002524.5:c.183A>C
NP_002515.1:p.(Q61H)
Likely Pathogenic
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NRAS
NM_002524.5:c.35G>A
NP_002515.1:p.(G12D)
VUS
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NRAS
NM_002524.4:c.35G>A
NP_002515.1:p.(G12D)
Likely Pathogenic
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NRAS
NM_002524.4:c.34G>T
NP_002515.1:p.(G12C)
Pathogenic
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NRAS
NM_002524.5:c.35G>T
NP_002515.1:p.(G12V)
Pathogenic
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NRAS
NM_002524.4:c.291-8G>A
NP_002515.1:p.?
VUS
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NRAS
NM_002524.4:c.159G>A
NP_002515.1:p.(L53=)
Benign
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NRAS
NM_002524.4:c.31G>A
NP_002515.1:p.(A11T)
VUS
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NRAS
NM_002524.4:c.71T>A
NP_002515.1:p.(I24N)
Likely Pathogenic
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NRAS
NM_002524.4:c.368G>A
NP_002515.1:p.(R123K)
VUS
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NRAS
NM_002524.4:c.173C>T
NP_002515.1:p.(T58I)
VUS
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NRAS
NM_002524.4:c.112-8A>G
NP_002515.1:p.?
Likely Benign
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NRAS
NM_002524.4:c.176C>A
NP_002515.1:p.(A59D)
VUS
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