C0796275[trait identifier] AND "Labcorp Genetics (formerly Invitae), L - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 646105	NM_000240.4(MAOA):c.3G>A (p.Met1Ile)	MAOA (M1I)	Single nucleotide variant (missense variant +2 more)	Brunner syndrome	GUncertain significance
Select item 1611732	NM_000240.4(MAOA):c.15G>A (p.Glu5=)	MAOA	Single nucleotide variant (synonymous variant +1 more)	Brunner syndrome	GLikely benign
Select item 755208	NM_000240.4(MAOA):c.30G>A (p.Ala10=)	MAOA	Single nucleotide variant (synonymous variant +1 more)	Brunner syndrome	GLikely benign
Select item 2812238	NM_000240.4(MAOA):c.56T>C (p.Ile19Thr)	MAOA (I19T)	Single nucleotide variant (missense variant +1 more)	Brunner syndrome	GUncertain significance
Select item 2806648	NM_000240.4(MAOA):c.73+19G>C	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 2897222	NM_000240.4(MAOA):c.74-9T>A	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 769174	NM_000240.4(MAOA):c.74-6C>T	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 1446772	NM_000240.4(MAOA):c.109G>A (p.Val37Ile)	MAOA (V37I)	Single nucleotide variant (missense variant +1 more)	Brunner syndrome	GUncertain significance
Select item 2912408	NM_000240.4(MAOA):c.163A>C (p.Ile55Leu)	MAOA (I55L)	Single nucleotide variant (missense variant +1 more)	Brunner syndrome	GUncertain significance
Select item 2698771	NM_000240.4(MAOA):c.163A>G (p.Ile55Val)	MAOA (I55V)	Single nucleotide variant (missense variant +1 more)	Brunner syndrome	GUncertain significance
Select item 718979	NM_000240.4(MAOA):c.168+11_168+15del	MAOA	Deletion (intron variant)	Brunner syndrome	GBenign
Select item 2730520	NM_000240.4(MAOA):c.186C>T (p.Tyr62=)	MAOA	Single nucleotide variant (synonymous variant +1 more)	Brunner syndrome	GLikely benign
Select item 3017094	NM_000240.4(MAOA):c.188T>C (p.Val63Ala)	MAOA (V63A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 726627	NM_000240.4(MAOA):c.255C>G (p.Gly85=)	MAOA	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 650306	NM_000240.4(MAOA):c.260A>G (p.Glu87Gly)	MAOA (E87G)	Single nucleotide variant (missense variant +1 more)	Brunner syndrome	GUncertain significance
Select item 1418704	NM_000240.4(MAOA):c.290T>C (p.Leu97Pro)	MAOA (L97P)	Single nucleotide variant (missense variant +1 more)	Brunner syndrome	GUncertain significance
Select item 1601403	NM_000240.4(MAOA):c.306+16C>A	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome +1 more	GBenign
Select item 2152492	NM_000240.4(MAOA):c.306+18C>A	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 2718102	NM_000240.4(MAOA):c.307-19G>C	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 2095297	NM_000240.4(MAOA):c.307-18T>C	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 1361377	NM_000240.4(MAOA):c.325C>T (p.Arg109Trp)	MAOA (R109W)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GUncertain significance
Select item 977422	NM_000240.4(MAOA):c.331G>A (p.Ala111Thr)	MAOA (A111T)	Single nucleotide variant (missense variant +1 more)	Brunner syndrome	GUncertain significance
Select item 1333950	NM_000240.4(MAOA):c.374A>G (p.Asn125Ser)	MAOA (N125S)	Single nucleotide variant (missense variant +1 more)	Brunner syndrome	GUncertain significance
Select item 129585	NM_000240.4(MAOA):c.385A>C (p.Arg129=)	MAOA	Single nucleotide variant (synonymous variant +1 more)	Brunner syndrome +3 more	GBenign
Select item 571290	NM_000240.4(MAOA):c.402G>A (p.Met134Ile)	MAOA (M134I +1 more)	Single nucleotide variant (missense variant +1 more)	Brunner syndrome +1 more	GUncertain significance
Select item 2726923	NM_000240.4(MAOA):c.412-20G>A	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 1614118	NM_000240.4(MAOA):c.412-13C>T	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 435813	NM_000240.4(MAOA):c.412-6C>G	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome +2 more	GLikely benign
Select item 2903491	NM_000240.4(MAOA):c.421G>A (p.Asp141Asn)	MAOA (D141N +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 1438897	NM_000240.4(MAOA):c.482T>C (p.Ile161Thr)	MAOA (I161T +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 435814	NM_000240.4(MAOA):c.515G>A (p.Arg172Gln)	MAOA (R172Q +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome +3 more	GBenign
Select item 2128067	NM_000240.4(MAOA):c.576G>T (p.Leu192=)	MAOA	Single nucleotide variant (synonymous variant)	Brunner syndrome	GLikely benign
Select item 2407239	NM_000240.4(MAOA):c.635A>G (p.Asn212Ser)	MAOA (N79S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2905825	NM_000240.4(MAOA):c.645+13T>A	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GUncertain significance
Select item 2074487	NM_000240.4(MAOA):c.650G>A (p.Arg217Gln)	MAOA (R217Q +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 1537792	NM_000240.4(MAOA):c.681C>T (p.Ser227=)	MAOA	Single nucleotide variant (synonymous variant)	Brunner syndrome +1 more	GLikely benign
Select item 722280	NM_000240.4(MAOA):c.702C>T (p.Leu234=)	MAOA	Single nucleotide variant (synonymous variant)	Brunner syndrome	GLikely benign
Select item 1391867	NM_000240.4(MAOA):c.703G>A (p.Gly235Arg)	MAOA (G235R +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 720971	NM_000240.4(MAOA):c.732C>T (p.Val244=)	MAOA	Single nucleotide variant (synonymous variant)	Brunner syndrome	GLikely benign
Select item 2965279	NM_000240.4(MAOA):c.736C>A (p.His246Asn)	MAOA (H113N +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 975746	NM_000240.4(MAOA):c.739G>A (p.Val247Ile)	MAOA (V114I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1491119	NM_000240.4(MAOA):c.766A>G (p.Ile256Val)	MAOA (I123V +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1760453	NM_000240.4(MAOA):c.774G>A (p.Thr258=)	MAOA	Single nucleotide variant (synonymous variant)	Brunner syndrome +1 more	GLikely benign
Select item 2697823	NM_000240.4(MAOA):c.796-15T>G	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 1156171	NM_000240.4(MAOA):c.796-9G>A	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 2150121	NM_000240.4(MAOA):c.804C>T (p.Tyr268=)	MAOA	Single nucleotide variant (synonymous variant)	Brunner syndrome	GLikely benign
Select item 1064570	NM_000240.4(MAOA):c.805G>A (p.Val269Ile)	MAOA (V136I +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 1496962	NM_000240.4(MAOA):c.812A>G (p.Asn271Ser)	MAOA (N138S +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 732079	NM_000240.4(MAOA):c.816G>A (p.Ala272=)	MAOA	Single nucleotide variant (synonymous variant)	Brunner syndrome	GBenign
Select item 198701	NM_000240.4(MAOA):c.825G>A (p.Pro275=)	MAOA	Single nucleotide variant (synonymous variant)	Brunner syndrome +2 more	GConflicting classifications of pathogenicity
Select item 2870983	NM_000240.4(MAOA):c.831G>A (p.Leu277=)	MAOA	Single nucleotide variant (synonymous variant)	Brunner syndrome	GLikely benign
Select item 567389	NM_000240.4(MAOA):c.890G>A (p.Arg297Gln)	MAOA (R297Q +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 92664	NM_000240.4(MAOA):c.891G>T (p.Arg297=)	MAOA	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +3 more	GBenign
Select item 2870984	NM_000240.4(MAOA):c.933G>A (p.Lys311=)	MAOA	Single nucleotide variant (synonymous variant)	Brunner syndrome	GLikely benign
Select item 2060608	NM_000240.4(MAOA):c.955+4G>A	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GUncertain significance
Select item 1545771	NM_000240.4(MAOA):c.956-8T>G	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 2913554	NM_000240.4(MAOA):c.1052+4G>C	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GUncertain significance
Select item 1674092	NM_000240.4(MAOA):c.1052+14G>A	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 1942663	NM_000240.4(MAOA):c.1052+17T>G	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 763299	NM_000240.4(MAOA):c.1053-10C>G	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 2893850	NM_000240.4(MAOA):c.1094A>G (p.His365Arg)	MAOA (H365R +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 2985275	NM_000240.4(MAOA):c.1106+15C>T	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 1673708	NM_000240.4(MAOA):c.1119C>A (p.Ile373=)	MAOA	Single nucleotide variant (synonymous variant)	Brunner syndrome	GLikely benign
Select item 1385383	NM_000240.4(MAOA):c.1153G>A (p.Glu385Lys)	MAOA (E385K +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 2017878	NM_000240.4(MAOA):c.1164+7A>C	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 2040131	NM_000240.4(MAOA):c.1165-18T>G	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GBenign
Select item 1166156	NM_000240.4(MAOA):c.1165-13C>T	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GBenign
Select item 1591308	NM_000240.4(MAOA):c.1165-11C>T	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 1074868	NM_000240.4(MAOA):c.1214del (p.Gly405fs)	MAOA (G272fs +1 more)	Deletion (frameshift variant)	Brunner syndrome	GPathogenic
Select item 2123659	NM_000240.4(MAOA):c.1215C>T (p.Gly405=)	MAOA	Single nucleotide variant (synonymous variant)	Brunner syndrome	GLikely benign
Select item 1448307	NM_000240.4(MAOA):c.1223C>T (p.Thr408Met)	MAOA (T275M +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 282807	NM_000240.4(MAOA):c.1248G>A (p.Met416Ile)	MAOA (M416I +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2012172	NM_000240.4(MAOA):c.1253A>G (p.Gln418Arg)	MAOA (Q285R +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 1592457	NM_000240.4(MAOA):c.1262+6A>G	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 1147557	NM_000240.4(MAOA):c.1262+7C>T	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 1627611	NM_000240.4(MAOA):c.1262+18C>T	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 1585186	NM_000240.4(MAOA):c.1262+19G>A	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 2044281	NM_000240.4(MAOA):c.1263-16C>G	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GBenign
Select item 2724563	NM_000240.4(MAOA):c.1279G>A (p.Val427Met)	MAOA (V294M +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 1946510	NM_000240.4(MAOA):c.1279G>T (p.Val427Leu)	MAOA (V294L +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 2154547	NM_000240.4(MAOA):c.1299G>A (p.Ala433=)	MAOA	Single nucleotide variant (synonymous variant)	Brunner syndrome	GLikely benign
Select item 1407025	NM_000240.4(MAOA):c.1361G>A (p.Arg454Gln)	MAOA (R321Q +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 1600000	NM_000240.4(MAOA):c.1374+19G>A	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GBenign
Select item 1671438	NM_000240.4(MAOA):c.1375-17T>C	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 2030833	NM_000240.4(MAOA):c.1375-14T>C	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 1630046	NM_000240.4(MAOA):c.1389C>T (p.Leu463=)	MAOA	Single nucleotide variant (synonymous variant)	Brunner syndrome	GLikely benign
Select item 3022858	NM_000240.4(MAOA):c.1390G>A (p.Gly464Arg)	MAOA (G331R +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 2167098	NM_000240.4(MAOA):c.1401C>T (p.Thr467=)	MAOA	Single nucleotide variant (synonymous variant)	Brunner syndrome	GLikely benign
Select item 92663	NM_000240.4(MAOA):c.1410T>C (p.Asp470=)	MAOA	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 2060826	NM_000240.4(MAOA):c.1418T>C (p.Val473Ala)	MAOA (V473A +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 2106514	NM_000240.4(MAOA):c.1437+4A>T	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GUncertain significance
Select item 2035985	NM_000240.4(MAOA):c.1437+11T>C	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 1595703	NM_000240.4(MAOA):c.1437+14C>T	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GLikely benign
Select item 1434925	NM_000240.4(MAOA):c.1438-3T>C	MAOA	Single nucleotide variant (intron variant)	Brunner syndrome	GUncertain significance
Select item 1035352	NM_000240.4(MAOA):c.1440C>A (p.Asp480Glu)	MAOA (D480E +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 1394005	NM_000240.4(MAOA):c.1441G>A (p.Val481Ile)	MAOA (V348I +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome	GUncertain significance
Select item 1772862	NM_000240.4(MAOA):c.1449G>A (p.Ala483=)	MAOA	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 792312	NM_000240.4(MAOA):c.1488C>G (p.Pro496=)	MAOA	Single nucleotide variant (synonymous variant)	Brunner syndrome	GLikely benign
Select item 727173	NM_000240.4(MAOA):c.1526C>T (p.Thr509Ile)	MAOA (T376I +1 more)	Single nucleotide variant (missense variant)	Brunner syndrome +1 more	GLikely benign
Select item 728527	NM_000240.4(MAOA):c.1545G>T (p.Gly515=)	MAOA	Single nucleotide variant (synonymous variant)	Brunner syndrome	GLikely benign

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