Project HERA
RET variants
Every RET variant the pipeline has interpreted, classified against the ClinGen expert-panel specification for the gene where one exists.
RET variants
Newest first. Each row opens the full report, criterion by criterion.
Variant
Protein change
Classification
RET
NM_020975.6:c.2944C>T
NP_066124.1:p.(R982C)
Likely Benign
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RET
NM_020975.6:c.2073T>C
NP_066124.1:p.(G691=)
VUS
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RET
NM_020975.5:c.1837C>A
NP_066124.1:p.(P613T)
VUS
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RET
NM_020975.5:c.2486G>A
NP_066124.1:p.(S829N)
VUS
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RET
NM_020975.5:c.2895G>T
NP_066124.1:p.(K965N)
VUS
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RET
NM_020975.6:c.1783G>A
NP_066124.1:p.(E595K)
VUS
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RET
NM_020975.5:c.2434del
NP_066124.1:p.(L812Cfs*57)
Likely Pathogenic
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RET
NM_020975.6:c.2689C>T
NP_066124.1:p.(R897*)
Pathogenic
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RET
NM_020975.6:c.2711C>T
NP_066124.1:p.(S904F)
Likely Pathogenic
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RET
NM_020975.6:c.2776C>T
NP_066124.1:p.(H926Y)
VUS
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RET
NM_020975.6:c.2410G>T
NP_066124.1:p.(V804L)
Likely Pathogenic
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