"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "SLC2A9" - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 350194	NM_020041.3(SLC2A9):c.1599T>C (p.Asp533=)	SLC2A9	Single nucleotide variant (synonymous variant)	Hypouricemia, renal, 2 +1 more	GBenign
Select item 350195	NM_020041.3(SLC2A9):c.1545C>T (p.Ser515=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1504763	NM_020041.3(SLC2A9):c.1518C>G (p.Thr506=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1001841	NM_020041.3(SLC2A9):c.1511A>T (p.Asn504Ile)	SLC2A9 (N475I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1350061	NM_020041.3(SLC2A9):c.1459A>G (p.Ile487Val)	SLC2A9 (I458V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2173069	NM_020041.3(SLC2A9):c.1420-6C>T	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1165550	NM_020041.3(SLC2A9):c.1420-19del	SLC2A9	Deletion (intron variant)	not provided +1 more	GBenign
Select item 1651490	NM_020041.3(SLC2A9):c.1419+16del	SLC2A9	Deletion (intron variant)	not provided	GLikely benign
Select item 2203533	NM_020041.3(SLC2A9):c.1419+1G>A	SLC2A9	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 1016658	NM_020041.3(SLC2A9):c.1386C>G (p.Asn462Lys)	SLC2A9 (N433K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1917981	NM_020041.3(SLC2A9):c.1385A>G (p.Asn462Ser)	SLC2A9 (N433S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1917079	NM_020041.3(SLC2A9):c.1383C>T (p.Ser461=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2069944	NM_020041.3(SLC2A9):c.1369G>A (p.Val457Ile)	SLC2A9 (V428I +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1080022	NM_020041.3(SLC2A9):c.1344G>A (p.Pro448=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1928845	NM_020041.3(SLC2A9):c.1339C>T (p.Arg447Trp)	SLC2A9 (R447W +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 905316	NM_020041.3(SLC2A9):c.1302G>A (p.Pro434=)	SLC2A9	Single nucleotide variant (synonymous variant)	Hypouricemia, renal, 2 +1 more	GBenign/Likely benign
Select item 350201	NM_020041.3(SLC2A9):c.1299C>T (p.Ile433=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 736857	NM_020041.3(SLC2A9):c.1292-6C>T	SLC2A9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2969198	NM_020041.3(SLC2A9):c.1291+16C>A	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2080711	NM_020041.3(SLC2A9):c.1291+9C>T	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2961021	NM_020041.3(SLC2A9):c.1291+6G>A	SLC2A9	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2810823	NM_020041.3(SLC2A9):c.1287del (p.Pro430fs)	SLC2A9 (P430fs +1 more)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 1993438	NM_020041.3(SLC2A9):c.1255A>G (p.Ile419Val)	SLC2A9 (I390V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 350202	NM_020041.3(SLC2A9):c.1221C>T (p.His407=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 2050846	NM_020041.3(SLC2A9):c.1215+8G>A	SLC2A9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1665070	NM_020041.3(SLC2A9):c.1215+7C>T	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 957465	NM_020041.3(SLC2A9):c.1215+4A>G	SLC2A9	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 350203	NM_020041.3(SLC2A9):c.1203G>A (p.Thr401=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2707485	NM_020041.3(SLC2A9):c.1197C>G (p.Thr399=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1388422	NM_020041.3(SLC2A9):c.1184T>C (p.Phe395Ser)	SLC2A9 (F366S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2858075	NM_020041.3(SLC2A9):c.1152C>T (p.Leu384=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1523026	NM_020041.3(SLC2A9):c.1139G>A (p.Arg380Gln)	SLC2A9 (R351Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 4596	NM_020041.3(SLC2A9):c.1138C>T (p.Arg380Trp)	SLC2A9 (R380W +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1151314	NM_020041.3(SLC2A9):c.1114-29CT[8]	SLC2A9	Microsatellite (intron variant)	not provided +1 more	GLikely benign
Select item 1920859	NM_020041.3(SLC2A9):c.1114-19C>T	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1987243	NM_020041.3(SLC2A9):c.1113+16G>A	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 350205	NM_020041.3(SLC2A9):c.1113+9A>C	SLC2A9	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 2174202	NM_020041.3(SLC2A9):c.1065C>T (p.Tyr355=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2180218	NM_020041.3(SLC2A9):c.1059C>G (p.Ile353Met)	SLC2A9 (I324M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1599340	NM_020041.3(SLC2A9):c.1050G>A (p.Pro350=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 350207	NM_020041.3(SLC2A9):c.1049C>T (p.Pro350Leu)	SLC2A9 (P350L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 350208	NM_020041.3(SLC2A9):c.1046C>T (p.Pro349Leu)	SLC2A9 (P320L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2979627	NM_020041.3(SLC2A9):c.1002+17G>A	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1661310	NM_020041.3(SLC2A9):c.1002+16C>T	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1653744	NM_020041.3(SLC2A9):c.1002+11G>A	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 350209	NM_020041.3(SLC2A9):c.957C>T (p.Thr319=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 906925	NM_020041.3(SLC2A9):c.937G>A (p.Val313Ile)	SLC2A9 (V313I +1 more)	Single nucleotide variant (missense variant)	Hypouricemia, renal, 2 +1 more	GUncertain significance
Select item 906926	NM_020041.3(SLC2A9):c.909C>T (p.Ser303=)	SLC2A9	Single nucleotide variant (synonymous variant)	Hypouricemia, renal, 2 +1 more	GBenign/Likely benign
Select item 350210	NM_020041.3(SLC2A9):c.899G>A (p.Arg300His)	SLC2A9 (R300H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 350211	NM_020041.3(SLC2A9):c.898C>T (p.Arg300Cys)	SLC2A9 (R300C +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 350212	NM_020041.3(SLC2A9):c.883G>A (p.Val295Met)	SLC2A9 (V295M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 350213	NM_020041.3(SLC2A9):c.881G>A (p.Arg294His)	SLC2A9 (R265H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1559795	NM_020041.3(SLC2A9):c.864G>A (p.Glu288=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 350215	NM_020041.3(SLC2A9):c.844G>A (p.Val282Ile)	SLC2A9 (V253I +1 more)	Single nucleotide variant (missense variant)	Hypouricemia, renal, 2 +1 more	GBenign
Select item 350217	NM_020041.3(SLC2A9):c.841G>C (p.Asp281His)	SLC2A9 (D252H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2076725	NM_020041.3(SLC2A9):c.832G>A (p.Gly278Ser)	SLC2A9 (G278S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1643942	NM_020041.3(SLC2A9):c.825G>A (p.Thr275=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 350218	NM_020041.3(SLC2A9):c.824C>T (p.Thr275Met)	SLC2A9 (T246M +1 more)	Single nucleotide variant (missense variant)	Hypouricemia, renal, 2 +1 more	GBenign
Select item 2993727	NM_020041.3(SLC2A9):c.815-16G>A	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1988900	NM_020041.3(SLC2A9):c.815-18G>A	SLC2A9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 350219	NM_020041.3(SLC2A9):c.809T>C (p.Val270Ala)	SLC2A9 (V241A +1 more)	Single nucleotide variant (missense variant)	Hypouricemia, renal, 2 +1 more	GBenign
Select item 1986558	NM_020041.3(SLC2A9):c.802A>C (p.Arg268=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1106602	NM_020041.3(SLC2A9):c.795C>T (p.Asn265=)	SLC2A9	Single nucleotide variant (synonymous variant)	Hypouricemia, renal, 2 +1 more	GLikely benign
Select item 1359926	NM_020041.3(SLC2A9):c.770G>T (p.Arg257Leu)	SLC2A9 (R228L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1381478	NM_020041.3(SLC2A9):c.769C>T (p.Arg257Cys)	SLC2A9 (R257C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2192042	NM_020041.3(SLC2A9):c.768A>C (p.Pro256=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2419307	NM_020041.3(SLC2A9):c.756C>T (p.Leu252=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 904605	NM_020041.3(SLC2A9):c.727G>A (p.Val243Ile)	SLC2A9 (V214I +1 more)	Single nucleotide variant (missense variant)	Hypouricemia, renal, 2 +1 more	GConflicting classifications of pathogenicity
Select item 1096161	NM_020041.3(SLC2A9):c.726C>T (p.Ala242=)	SLC2A9	Single nucleotide variant (synonymous variant)	Hypouricemia, renal, 2 +1 more	GLikely benign
Select item 2958428	NM_020041.3(SLC2A9):c.723T>A (p.Pro241=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1046785	NM_020041.3(SLC2A9):c.713T>C (p.Ile238Thr)	SLC2A9 (I238T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3020786	NM_020041.3(SLC2A9):c.682-19G>A	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 350233	NM_020041.3(SLC2A9):c.681+13C>T	SLC2A9	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 350234	NM_020041.3(SLC2A9):c.666C>T (p.Pro222=)	SLC2A9	Single nucleotide variant (synonymous variant)	Hypouricemia, renal, 2 +1 more	GBenign/Likely benign
Select item 1970760	NM_020041.3(SLC2A9):c.625A>T (p.Ile209Phe)	SLC2A9 (I180F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2792651	NM_020041.3(SLC2A9):c.612G>A (p.Val204=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1422868	NM_020041.3(SLC2A9):c.599C>T (p.Ser200Phe)	SLC2A9 (S171F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 4597	NM_020041.3(SLC2A9):c.592C>T (p.Arg198Cys)	SLC2A9 (R198C +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1938288	NM_020041.3(SLC2A9):c.567T>A (p.Leu189=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 350235	NM_020041.3(SLC2A9):c.567T>C (p.Leu189=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2703740	NM_020041.3(SLC2A9):c.564C>T (p.Tyr188=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1901385	NM_020041.3(SLC2A9):c.546C>T (p.Leu182=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2148495	NM_020041.3(SLC2A9):c.541G>A (p.Ala181Thr)	SLC2A9 (A152T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1918944	NM_020041.3(SLC2A9):c.540C>T (p.Val180=)	SLC2A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1017579	NM_020041.3(SLC2A9):c.538G>A (p.Val180Ile)	SLC2A9 (V151I +1 more)	Single nucleotide variant (missense variant)	Hypouricemia, renal, 2 +1 more	GUncertain significance
Select item 2035711	NM_020041.3(SLC2A9):c.536-7T>C	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1530542	NM_020041.3(SLC2A9):c.536-18T>A	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1901914	NM_020041.3(SLC2A9):c.535+19G>A	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2957702	NM_020041.3(SLC2A9):c.535+18C>T	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2790433	NM_020041.3(SLC2A9):c.535+10C>A	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 350236	NM_020041.3(SLC2A9):c.504C>T (p.Ile168=)	SLC2A9	Single nucleotide variant (synonymous variant)	Hypouricemia, renal, 2 +1 more	GBenign
Select item 2082462	NM_020041.3(SLC2A9):c.445A>G (p.Ile149Val)	SLC2A9 (I149V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1979732	NM_020041.3(SLC2A9):c.431A>G (p.Asn144Ser)	SLC2A9 (N115S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2127191	NM_020041.3(SLC2A9):c.422T>C (p.Leu141Ser)	SLC2A9 (L112S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2106755	NM_020041.3(SLC2A9):c.411-14T>C	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2022714	NM_020041.3(SLC2A9):c.411-19A>T	SLC2A9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1897759	NM_020041.3(SLC2A9):c.403C>A (p.Leu135Ile)	SLC2A9, SLC2A9-AS1 (L106I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 350237	NM_020041.3(SLC2A9):c.375G>A (p.Thr125=)	SLC2A9, SLC2A9-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2113538	NM_020041.3(SLC2A9):c.372dup (p.Thr125fs)	SLC2A9, SLC2A9-AS1 (T96fs +1 more)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 350238	NM_020041.3(SLC2A9):c.354dup (p.Ile119fs)	SLC2A9, SLC2A9-AS1 (I90fs +1 more)	Duplication (frameshift variant)	Hypouricemia, renal, 2 +1 more	GConflicting classifications of pathogenicity

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