"Invitae"[submitter] AND "SLC9A3"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1394829	NM_004174.4(SLC9A3):c.2502G>C (p.Met834Ile)	SLC9A3, SLC9A3-AS1 (M825I +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 1907910	NM_004174.4(SLC9A3):c.2502-5C>T	SLC9A3, SLC9A3-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2965286	NM_004174.4(SLC9A3):c.2502-7C>T	SLC9A3, SLC9A3-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1923367	NM_004174.4(SLC9A3):c.2502-12C>T	SLC9A3, SLC9A3-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1629539	NM_004174.4(SLC9A3):c.2502-15C>T	SLC9A3, SLC9A3-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1644088	NM_004174.4(SLC9A3):c.2502-18C>T	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2844651	NM_004174.4(SLC9A3):c.2501+21G>A	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1662418	NM_004174.4(SLC9A3):c.2501+16C>T	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1666995	NM_004174.4(SLC9A3):c.2501+15C>T	SLC9A3-AS1, SLC9A3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1593529	NM_004174.4(SLC9A3):c.2501+14G>A	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3006927	NM_004174.4(SLC9A3):c.2501+11C>G	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1536746	NM_004174.4(SLC9A3):c.2501+11C>T	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1904457	NM_004174.4(SLC9A3):c.2491T>C (p.Ser831Pro)	SLC9A3-AS1, SLC9A3 (S822P +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2182430	NM_004174.4(SLC9A3):c.2487C>G (p.Pro829=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1545696	NM_004174.4(SLC9A3):c.2484C>G (p.Leu828=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2065002	NM_004174.4(SLC9A3):c.2480C>A (p.Ala827Asp)	SLC9A3, SLC9A3-AS1 (A827D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1487700	NM_004174.4(SLC9A3):c.2470C>A (p.Pro824Thr)	SLC9A3, SLC9A3-AS1 (P815T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2098836	NM_004174.4(SLC9A3):c.2469G>A (p.Arg823=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2787888	NM_004174.4(SLC9A3):c.2460C>G (p.Pro820=)	SLC9A3-AS1, SLC9A3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1656768	NM_004174.4(SLC9A3):c.2439C>T (p.Ser813=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1377109	NM_004174.4(SLC9A3):c.2427G>C (p.Lys809Asn)	SLC9A3, SLC9A3-AS1 (K809N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1388440	NM_004174.4(SLC9A3):c.2423G>A (p.Ser808Asn)	SLC9A3, SLC9A3-AS1 (S808N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1511537	NM_004174.4(SLC9A3):c.2410T>A (p.Phe804Ile)	SLC9A3, SLC9A3-AS1 (F795I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1905883	NM_004174.4(SLC9A3):c.2403G>A (p.Leu801=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3023837	NM_004174.4(SLC9A3):c.2401C>T (p.Leu801=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1168112	NM_004174.4(SLC9A3):c.2395T>C (p.Cys799Arg)	SLC9A3, SLC9A3-AS1 (C790R +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1468314	NM_004174.4(SLC9A3):c.2393T>G (p.Phe798Cys)	SLC9A3, SLC9A3-AS1 (F789C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1429270	NM_004174.4(SLC9A3):c.2390C>G (p.Thr797Ser)	SLC9A3, SLC9A3-AS1 (T797S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1474601	NM_004174.4(SLC9A3):c.2386G>C (p.Gly796Arg)	SLC9A3, SLC9A3-AS1 (G787R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1439456	NM_004174.4(SLC9A3):c.2386G>A (p.Gly796Ser)	SLC9A3, SLC9A3-AS1 (G787S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2849118	NM_004174.4(SLC9A3):c.2376del (p.Tyr793fs)	SLC9A3, SLC9A3-AS1 (Y784fs +1 more)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 1599087	NM_004174.4(SLC9A3):c.2373T>A (p.Ile791=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1670097	NM_004174.4(SLC9A3):c.2361C>T (p.Ala787=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1655594	NM_004174.4(SLC9A3):c.2358G>A (p.Arg786=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1093879	NM_004174.4(SLC9A3):c.2343G>A (p.Val781=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2152459	NM_004174.4(SLC9A3):c.2342T>C (p.Val781Ala)	SLC9A3, SLC9A3-AS1 (V781A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1548843	NM_004174.4(SLC9A3):c.2334G>A (p.Gly778=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1353656	NM_004174.4(SLC9A3):c.2329C>G (p.Pro777Ala)	SLC9A3, SLC9A3-AS1 (P777A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1632498	NM_004174.4(SLC9A3):c.2325G>A (p.Leu775=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1572319	NM_004174.4(SLC9A3):c.2319C>T (p.Pro773=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2790117	NM_004174.4(SLC9A3):c.2316G>T (p.Pro772=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1928096	NM_004174.4(SLC9A3):c.2303T>C (p.Leu768Pro)	SLC9A3, SLC9A3-AS1 (L759P +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1490669	NM_004174.4(SLC9A3):c.2294G>A (p.Arg765His)	SLC9A3, SLC9A3-AS1 (R756H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1139880	NM_004174.4(SLC9A3):c.2292C>T (p.Asp764=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1081283	NM_004174.4(SLC9A3):c.2285C>A (p.Ala762Asp)	SLC9A3, SLC9A3-AS1 (A753D +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2072410	NM_004174.4(SLC9A3):c.2277G>A (p.Pro759=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1938106	NM_004174.4(SLC9A3):c.2276C>T (p.Pro759Leu)	SLC9A3, SLC9A3-AS1 (P759L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1498262	NM_004174.4(SLC9A3):c.2270T>G (p.Phe757Cys)	SLC9A3, SLC9A3-AS1 (F757C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1355830	NM_004174.4(SLC9A3):c.2266G>A (p.Val756Met)	SLC9A3, SLC9A3-AS1 (V747M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2881555	NM_004174.4(SLC9A3):c.2265T>C (p.Pro755=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1947912	NM_004174.4(SLC9A3):c.2255T>C (p.Ile752Thr)	SLC9A3, SLC9A3-AS1 (I743T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1720737	NM_004174.4(SLC9A3):c.2254A>G (p.Ile752Val)	SLC9A3, SLC9A3-AS1 (I743V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1570263	NM_004174.4(SLC9A3):c.2252-5C>T	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant +1 more)	not provided	GLikely benign
Select item 2174620	NM_004174.4(SLC9A3):c.2252-7C>A	SLC9A3, SLC9A3-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1674253	NM_004174.4(SLC9A3):c.2252-17G>A	SLC9A3, SLC9A3-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1638728	NM_004174.4(SLC9A3):c.2252-18C>G	SLC9A3, SLC9A3-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1165827	NM_004174.4(SLC9A3):c.2252-18C>T	SLC9A3, SLC9A3-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1915766	NM_004174.4(SLC9A3):c.2252-20G>C	SLC9A3, SLC9A3-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1936961	NM_004174.4(SLC9A3):c.2251+20_2251+27del	SLC9A3, SLC9A3-AS1	Deletion (intron variant)	not provided	GLikely benign
Select item 2007722	NM_004174.4(SLC9A3):c.2251+18G>A	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3004059	NM_004174.4(SLC9A3):c.2251+17G>A	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2986443	NM_004174.4(SLC9A3):c.2251+16A>C	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2979440	NM_004174.4(SLC9A3):c.2251+12G>A	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1553172	NM_004174.4(SLC9A3):c.2251+9G>A	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2808385	NM_004174.4(SLC9A3):c.2244C>A (p.Ser748=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1558434	NM_004174.4(SLC9A3):c.2244C>T (p.Ser748=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1539663	NM_004174.4(SLC9A3):c.2235G>A (p.Ala745=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1660838	NM_004174.4(SLC9A3):c.2223C>A (p.Thr741=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1546948	NM_004174.4(SLC9A3):c.2223C>G (p.Thr741=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2417486	NM_004174.4(SLC9A3):c.2208C>T (p.Phe736=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1654886	NM_004174.4(SLC9A3):c.2205G>A (p.Glu735=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2788331	NM_004174.4(SLC9A3):c.2199G>T (p.Gly733=)	SLC9A3-AS1, SLC9A3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1428168	NM_004174.4(SLC9A3):c.2193T>G (p.Ser731Arg)	SLC9A3, SLC9A3-AS1 (S722R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1386987	NM_004174.4(SLC9A3):c.2190G>A (p.Met730Ile)	SLC9A3, SLC9A3-AS1 (M721I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1507705	NM_004174.4(SLC9A3):c.2182GAG[1] (p.Glu729del)	SLC9A3, SLC9A3-AS1 (E729del +1 more)	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 1544010	NM_004174.4(SLC9A3):c.2184G>A (p.Glu728=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1950643	NM_004174.4(SLC9A3):c.2181T>G (p.Asp727Glu)	SLC9A3, SLC9A3-AS1 (D718E +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1461130	NM_004174.4(SLC9A3):c.2179G>A (p.Asp727Asn)	SLC9A3, SLC9A3-AS1 (D718N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2740757	NM_004174.4(SLC9A3):c.2178T>C (p.Tyr726=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1471012	NM_004174.4(SLC9A3):c.2171C>T (p.Pro724Leu)	SLC9A3, SLC9A3-AS1 (P715L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2858340	NM_004174.4(SLC9A3):c.2166G>C (p.Glu722Asp)	SLC9A3, SLC9A3-AS1 (E722D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2869979	NM_004174.4(SLC9A3):c.2160C>T (p.Thr720=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 722287	NM_004174.4(SLC9A3):c.2158A>G (p.Thr720Ala)	SLC9A3, SLC9A3-AS1 (T711A +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1382490	NM_004174.4(SLC9A3):c.2157C>G (p.Asp719Glu)	SLC9A3, SLC9A3-AS1 (D710E +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1716282	NM_004174.4(SLC9A3):c.2150T>G (p.Leu717Arg)	SLC9A3, SLC9A3-AS1 (L708R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1557616	NM_004174.4(SLC9A3):c.2141-4C>T	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2988173	NM_004174.4(SLC9A3):c.2141-13C>T	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1667809	NM_004174.4(SLC9A3):c.2141-14C>T	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1632555	NM_004174.4(SLC9A3):c.2141-18C>T	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1932590	NM_004174.4(SLC9A3):c.2141-20C>T	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1657648	NM_004174.4(SLC9A3):c.2140+17del	SLC9A3, SLC9A3-AS1	Deletion (intron variant)	not provided	GLikely benign
Select item 1913986	NM_004174.4(SLC9A3):c.2140+12G>A	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1567086	NM_004174.4(SLC9A3):c.2140+12G>T	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2703924	NM_004174.4(SLC9A3):c.2140+8G>A	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1413953	NM_004174.4(SLC9A3):c.2140+4C>T	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1372276	NM_004174.4(SLC9A3):c.2140+4C>A	SLC9A3, SLC9A3-AS1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1389896	NM_004174.4(SLC9A3):c.2135A>G (p.Glu712Gly)	SLC9A3, SLC9A3-AS1 (E703G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2747281	NM_004174.4(SLC9A3):c.2127C>A (p.Thr709=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2088356	NM_004174.4(SLC9A3):c.2117A>G (p.Gln706Arg)	SLC9A3, SLC9A3-AS1 (Q697R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2727718	NM_004174.4(SLC9A3):c.2115G>C (p.Ala705=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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