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Items: 15

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SDHC
(R15*)
Single nucleotide variant
(nonsense +3 more)
Hereditary pheochromocytoma-paraganglioma
+5 more
GPathogenic
SDHC
(T33M +1 more)
Single nucleotide variant
(missense variant +3 more)
Hereditary pheochromocytoma-paraganglioma
+6 more
GUncertain significance
SDHC
(R40Q +2 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
SDHC
Single nucleotide variant
(synonymous variant +2 more)
Hereditary pheochromocytoma-paraganglioma
+5 more
GBenign/Likely benign
SDHC
(R50C +2 more)
Single nucleotide variant
(missense variant +2 more)
Gastrointestinal stromal tumor
+4 more
GPathogenic/Likely pathogenic
SDHC
(L39F +7 more)
Single nucleotide variant
(missense variant +2 more)
Paragangliomas 3
+3 more
GUncertain significance
SDHC
(Y99H +7 more)
Single nucleotide variant
(missense variant +2 more)
Gastrointestinal stromal tumor
+4 more
GConflicting classifications of pathogenicity
SDHC
Single nucleotide variant
(synonymous variant +2 more)
not specified
+6 more
GBenign/Likely benign
SDHC
(Y126C +7 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
+5 more
GPathogenic/Likely pathogenic
SDHC
(W129* +7 more)
Single nucleotide variant
(nonsense +2 more)
Gastrointestinal stromal tumor
+4 more
GPathogenic/Likely pathogenic
SDHC
(R133* +7 more)
Single nucleotide variant
(nonsense +2 more)
Hereditary cancer-predisposing syndrome
+5 more
GPathogenic
SDHC
Single nucleotide variant
(splice donor variant +1 more)
Hereditary pheochromocytoma-paraganglioma
+4 more
GPathogenic/Likely pathogenic
SDHC
(M164L +10 more)
Single nucleotide variant
(missense variant)
Ovarian cancer
+6 more
GConflicting classifications of pathogenicity
SDHD
Single nucleotide variant
(synonymous variant +2 more)
Cowden syndrome 3
+10 more
GBenign/Likely benign
SDHD
Single nucleotide variant
(synonymous variant +2 more)
Pheochromocytoma
+10 more
GBenign/Likely benign
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