"All of Us Research Program, National Institutes of Health"[submitter] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3074801	NM_003002.4(SDHD):c.-15G>T	LOC126861339, SDHD	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary pheochromocytoma-paraganglioma	GUncertain significance
Select item 3385998	NM_003002.4(SDHD):c.-12C>T	LOC126861339, SDHD	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary pheochromocytoma-paraganglioma	GLikely benign
Select item 3072494	NM_003002.4(SDHD):c.-9A>C	LOC126861339, SDHD	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary pheochromocytoma-paraganglioma	GLikely benign
Select item 619913	NM_003002.4(SDHD):c.-4C>T	LOC126861339, SDHD	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 3073916	NM_003002.4(SDHD):c.5C>A (p.Ala2Glu)	LOC126861339, SDHD (A2E)	Single nucleotide variant (missense variant +1 more)	Hereditary pheochromocytoma-paraganglioma	GUncertain significance
Select item 581402	NM_003002.4(SDHD):c.18G>T (p.Arg6Ser)	LOC126861339, SDHD (R6S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +5 more	GUncertain significance
Select item 239462	NM_003002.4(SDHD):c.18G>A (p.Arg6=)	LOC126861339, SDHD	Single nucleotide variant (synonymous variant +1 more)	not specified +7 more	GLikely benign
Select item 465227	NM_003002.4(SDHD):c.21G>A (p.Leu7=)	LOC126861339, SDHD	Single nucleotide variant (synonymous variant +1 more)	Hereditary pheochromocytoma-paraganglioma +5 more	GLikely benign
Select item 1619946	NM_003002.4(SDHD):c.27C>T (p.Ala9=)	LOC126861339, SDHD	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +5 more	GLikely benign
Select item 1631130	NM_003002.4(SDHD):c.33C>T (p.Cys11=)	LOC126861339, SDHD	Single nucleotide variant (synonymous variant +1 more)	Hereditary pheochromocytoma-paraganglioma +6 more	GLikely benign
Select item 533789	NM_003002.4(SDHD):c.37G>T (p.Ala13Ser)	LOC126861339, SDHD (A13S)	Single nucleotide variant (missense variant +1 more)	Pheochromocytoma +6 more	GUncertain significance
Select item 570468	NM_003002.4(SDHD):c.38C>T (p.Ala13Val)	LOC126861339, SDHD (A13V)	Single nucleotide variant (missense variant +1 more)	Carney-Stratakis syndrome +5 more	GUncertain significance
Select item 755556	NM_003002.4(SDHD):c.39C>T (p.Ala13=)	LOC126861339, SDHD	Single nucleotide variant (synonymous variant +1 more)	Cowden syndrome 3 +5 more	GLikely benign
Select item 947980	NM_003002.4(SDHD):c.49C>G (p.Arg17Gly)	LOC126861339, SDHD (R17G)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +7 more	GUncertain significance
Select item 1130962	NM_003002.4(SDHD):c.52+8dup	LOC126861339, SDHD	Duplication (intron variant)	Pheochromocytoma +4 more	GLikely benign