"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "SULT2B1 - ClinVar

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Items: 40

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 711605	NM_177973.2(SULT2B1):c.15C>T (p.Ala5=)	SULT2B1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 748807	NM_177973.2(SULT2B1):c.18G>A (p.Glu6=)	SULT2B1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2056152	NM_177973.2(SULT2B1):c.29C>T (p.Pro10Leu)	SULT2B1 (P10L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 790920	NM_177973.2(SULT2B1):c.98G>A (p.Arg33Gln)	SULT2B1 (R33Q +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1613054	NM_177973.2(SULT2B1):c.120C>T (p.Pro40=)	SULT2B1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2976267	NM_177973.2(SULT2B1):c.138C>T (p.Leu46=)	SULT2B1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 726656	NM_177973.2(SULT2B1):c.152T>C (p.Leu51Ser)	SULT2B1 (L36S +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 1368554	NM_177973.2(SULT2B1):c.181G>A (p.Asp61Asn)	SULT2B1 (D61N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2963085	NM_177973.2(SULT2B1):c.215-16C>T	SULT2B1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 737863	NM_177973.2(SULT2B1):c.215-6C>G	SULT2B1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 778850	NM_177973.2(SULT2B1):c.277C>T (p.Arg93Cys)	SULT2B1 (R93C +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1601562	NM_177973.2(SULT2B1):c.424-10C>T	SULT2B1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 799103	NM_177973.2(SULT2B1):c.426G>A (p.Val142=)	SULT2B1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 720878	NM_177973.2(SULT2B1):c.501G>A (p.Lys167=)	SULT2B1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 710148	NM_177973.2(SULT2B1):c.570C>T (p.Phe190=)	SULT2B1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2883545	NM_177973.2(SULT2B1):c.592C>T (p.Arg198Trp)	SULT2B1 (R183W +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 799104	NM_177973.2(SULT2B1):c.600G>A (p.Lys200=)	SULT2B1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 796345	NM_177973.2(SULT2B1):c.630C>T (p.Tyr210=)	SULT2B1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1098858	NM_177973.2(SULT2B1):c.637C>T (p.Leu213=)	SULT2B1	Single nucleotide variant (synonymous variant)	Ichthyosis, congenital, autosomal recessive 14 +1 more	GBenign
Select item 1655054	NM_177973.2(SULT2B1):c.689G>A (p.Arg230His)	SULT2B1 (R215H +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2865962	NM_177973.2(SULT2B1):c.694C>T (p.Leu232=)	SULT2B1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2883596	NM_177973.2(SULT2B1):c.718G>A (p.Val240Ile)	SULT2B1 (V240I +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1443354	NM_177973.2(SULT2B1):c.742G>A (p.Ala248Thr)	SULT2B1 (A233T +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 773358	NM_177973.2(SULT2B1):c.756C>T (p.Asn252=)	SULT2B1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2135708	NM_177973.2(SULT2B1):c.799C>T (p.His267Tyr)	SULT2B1 (H267Y +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2146948	NM_177973.2(SULT2B1):c.802C>T (p.Arg268Cys)	SULT2B1 (R253C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 782627	NM_177973.2(SULT2B1):c.803G>A (p.Arg268His)	SULT2B1 (R253H +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 737492	NM_177973.2(SULT2B1):c.807C>T (p.Arg269=)	SULT2B1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 719579	NM_177973.2(SULT2B1):c.826+3G>A	SULT2B1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2416791	NM_177973.2(SULT2B1):c.826+4C>T	SULT2B1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1265068	NM_177973.2(SULT2B1):c.834C>T (p.Cys278=)	SULT2B1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1967337	NM_177973.2(SULT2B1):c.858G>A (p.Thr286=)	SULT2B1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2044103	NM_177973.2(SULT2B1):c.904C>G (p.Arg302Gly)	SULT2B1 (R287G +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1591349	NM_177973.2(SULT2B1):c.912G>A (p.Met304Ile)	SULT2B1 (M289I +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2047113	NM_177973.2(SULT2B1):c.914C>T (p.Pro305Leu)	SULT2B1 (P305L +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2178014	NM_177973.2(SULT2B1):c.939G>A (p.Pro313=)	SULT2B1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1601174	NM_177973.2(SULT2B1):c.948C>T (p.Asp316=)	SULT2B1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1378138	NM_177973.2(SULT2B1):c.998T>C (p.Leu333Pro)	SULT2B1 (L318P +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1601533	NM_177973.2(SULT2B1):c.1034C>T (p.Pro345Leu)	SULT2B1 (P330L +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3242656	NC_000019.9:g.(?_48901650)_(49055600_?)dup	CYTH2, GRIN2D +4 more	Duplication	not provided	GUncertain significance

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Items: 40