Fam110a Variant Search Result - Rat Genome Database

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35 records found for search term Fam110a

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156059483	CV2305330	single nucleotide variant	NM_001042353.3(FAM110A):c.37G>A (p.Ala13Thr)	not specified [RCV004171242]	likely benign	20	844841	844841	Human		name
156131483	CV2372845	single nucleotide variant	NM_001042353.3(FAM110A):c.43G>A (p.Ala15Thr)	not specified [RCV004222027]	uncertain significance	20	844847	844847	Human		name
598223686	CV3965711	single nucleotide variant	NM_001042353.3(FAM110A):c.62G>C (p.Arg21Pro)	not specified [RCV005341191]	uncertain significance	20	844866	844866	Human		name
598223694	CV3965712	single nucleotide variant	NM_001042353.3(FAM110A):c.29C>T (p.Ala10Val)	not specified [RCV005341192]	uncertain significance	20	844833	844833	Human		name
155981784	CV2272896	single nucleotide variant	NM_001042353.3(FAM110A):c.145G>T (p.Asp49Tyr)	not specified [RCV004135795]	uncertain significance	20	844949	844949	Human		name
405724775	CV3249668	single nucleotide variant	NM_001042353.3(FAM110A):c.160G>A (p.Val54Ile)	not specified [RCV004378488]	uncertain significance	20	844964	844964	Human		name
405724784	CV3249669	single nucleotide variant	NM_001042353.3(FAM110A):c.181A>G (p.Asn61Asp)	not specified [RCV004378489]	uncertain significance	20	844985	844985	Human		name
597718897	CV3671830	single nucleotide variant	NM_001042353.3(FAM110A):c.248G>C (p.Arg83Pro)	not specified [RCV004918576]	uncertain significance	20	845052	845052	Human		name
597718905	CV3671831	single nucleotide variant	NM_001042353.3(FAM110A):c.185C>A (p.Thr62Asn)	not specified [RCV004918577]	uncertain significance	20	844989	844989	Human		name
156316321	CV2250894	single nucleotide variant	NM_001042353.3(FAM110A):c.607G>C (p.Glu203Gln)	not specified [RCV004123480]	uncertain significance	20	845411	845411	Human		name
155966671	CV2280096	single nucleotide variant	NM_001042353.3(FAM110A):c.776G>T (p.Arg259Leu)	not specified [RCV004146751]	uncertain significance	20	845580	845580	Human		name
156191488	CV2289353	single nucleotide variant	NM_001042353.3(FAM110A):c.579G>T (p.Glu193Asp)	not specified [RCV004152321]	uncertain significance	20	845383	845383	Human		name
156353222	CV2324124	single nucleotide variant	NM_001042353.3(FAM110A):c.386G>C (p.Arg129Pro)	not specified [RCV004178408]	uncertain significance	20	845190	845190	Human		name
156067680	CV2340985	single nucleotide variant	NM_001042353.3(FAM110A):c.743G>T (p.Cys248Phe)	not specified [RCV004181477]	uncertain significance	20	845547	845547	Human		name
156063630	CV2352784	single nucleotide variant	NM_001042353.3(FAM110A):c.389C>T (p.Ala130Val)	not specified [RCV004198799]	uncertain significance	20	845193	845193	Human		name
155963884	CV2395772	single nucleotide variant	NM_001042353.3(FAM110A):c.668A>G (p.His223Arg)	not specified [RCV004235301]	uncertain significance	20	845472	845472	Human		name
329361939	CV2468459	single nucleotide variant	NM_001042353.3(FAM110A):c.590G>A (p.Arg197Lys)	not specified [RCV004277764]	uncertain significance	20	845394	845394	Human		name
401731679	CV2693941	single nucleotide variant	NM_001042353.3(FAM110A):c.352G>A (p.Val118Met)	not specified [RCV004300236]	uncertain significance	20	845156	845156	Human		name
401740966	CV2702718	single nucleotide variant	NM_001042353.3(FAM110A):c.412C>G (p.Pro138Ala)	not specified [RCV004318967]	uncertain significance	20	845216	845216	Human		name
401757330	CV2734948	single nucleotide variant	NM_001042353.3(FAM110A):c.797A>G (p.Tyr266Cys)	not specified [RCV004333655]	uncertain significance	20	845601	845601	Human		name
405724793	CV3249670	single nucleotide variant	NM_001042353.3(FAM110A):c.334G>C (p.Asp112His)	not specified [RCV004378490]	uncertain significance	20	845138	845138	Human		name
405724800	CV3249671	single nucleotide variant	NM_001042353.3(FAM110A):c.380C>T (p.Pro127Leu)	not specified [RCV004378491]	uncertain significance	20	845184	845184	Human		name
405724808	CV3249672	single nucleotide variant	NM_001042353.3(FAM110A):c.431C>A (p.Pro144Gln)	not specified [RCV004378492]	uncertain significance	20	845235	845235	Human		name
405724816	CV3249673	single nucleotide variant	NM_001042353.3(FAM110A):c.451G>A (p.Val151Ile)	not specified [RCV004378493]	uncertain significance	20	845255	845255	Human		name
405724823	CV3249674	single nucleotide variant	NM_001042353.3(FAM110A):c.466G>A (p.Val156Ile)	not specified [RCV004378494]	uncertain significance	20	845270	845270	Human		name
405724832	CV3249675	single nucleotide variant	NM_001042353.3(FAM110A):c.802G>A (p.Val268Met)	not specified [RCV004378495]	uncertain significance	20	845606	845606	Human		name
407507747	CV3435386	single nucleotide variant	NM_001042353.3(FAM110A):c.523G>A (p.Ala175Thr)	not specified [RCV004625191]	uncertain significance	20	845327	845327	Human		name
597718862	CV3671826	single nucleotide variant	NM_001042353.3(FAM110A):c.580C>T (p.Arg194Cys)	not specified [RCV004918572]	uncertain significance	20	845384	845384	Human		name
597718871	CV3671827	single nucleotide variant	NM_001042353.3(FAM110A):c.748C>T (p.Arg250Cys)	not specified [RCV004918573]	uncertain significance	20	845552	845552	Human		name
597718880	CV3671828	single nucleotide variant	NM_001042353.3(FAM110A):c.628G>T (p.Gly210Cys)	not specified [RCV004918574]	uncertain significance	20	845432	845432	Human		name
597718889	CV3671829	single nucleotide variant	NM_001042353.3(FAM110A):c.518C>T (p.Ala173Val)	not specified [RCV004918575]	uncertain significance	20	845322	845322	Human		name
597718920	CV3671833	single nucleotide variant	NM_001042353.3(FAM110A):c.653G>T (p.Gly218Val)	not specified [RCV004918579]	uncertain significance	20	845457	845457	Human		name
598223701	CV3965713	single nucleotide variant	NM_001042353.3(FAM110A):c.409C>G (p.Pro137Ala)	not specified [RCV005341193]	uncertain significance	20	845213	845213	Human		name
598223709	CV3965714	single nucleotide variant	NM_001042353.3(FAM110A):c.520G>A (p.Ala174Thr)	not specified [RCV005341194]	uncertain significance	20	845324	845324	Human		name
15161985	CV728825	single nucleotide variant	NM_001042353.3(FAM110A):c.397G>C (p.Ala133Pro)	not provided [RCV000881673]	benign	20	845201	845201	Human		name

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