ClinVar for Gene (Select 22880) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3235788	NM_001303256.3(MORC2):c.329G>A (p.Arg110His)	MORC2 (R110H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3235749	NM_001303256.3(MORC2):c.810C>G (p.Cys270Trp)	MORC2 (C208W +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3067924	NM_001303256.3(MORC2):c.1604+1G>T	MORC2	Single nucleotide variant (splice donor variant)	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy	GUncertain significance
Select item 3061162	NM_001303256.3(MORC2):c.1051A>G (p.Arg351Gly)	MORC2 (R289G +1 more)	Single nucleotide variant (missense variant)	MORC2-related disorder	GUncertain significance
Select item 3055353	NM_001303256.3(MORC2):c.904+4dup	MORC2	Duplication (intron variant)	MORC2-related disorder	GLikely benign
Select item 3041758	NM_001303256.3(MORC2):c.226+9T>G	MORC2	Single nucleotide variant (intron variant)	MORC2-related disorder	GLikely benign
Select item 3029207	NM_001303256.3(MORC2):c.1458del (p.Lys486fs)	MORC2 (K424fs +1 more)	Deletion (frameshift variant)	MORC2-related disorder	GUncertain significance
Select item 3027016	NM_001303256.3(MORC2):c.1401G>A (p.Glu467=)	MORC2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3023002	NM_001303256.3(MORC2):c.1245T>A (p.Asp415Glu)	MORC2 (D353E +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 3017368	NM_001303256.3(MORC2):c.2751T>C (p.Asn917=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 3008788	NM_001303256.3(MORC2):c.518A>G (p.Tyr173Cys)	MORC2 (Y111C +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 3008377	NM_001303256.3(MORC2):c.2049G>A (p.Lys683=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 3005108	NM_001303256.3(MORC2):c.969C>T (p.Asp323=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 3004976	NM_001303256.3(MORC2):c.2535C>T (p.Gly845=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 3003193	NM_001303256.3(MORC2):c.1738-17T>A	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 3001311	NM_001303256.3(MORC2):c.1499-12dup	MORC2	Duplication (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GBenign
Select item 2983275	NM_001303256.3(MORC2):c.2622C>T (p.Gly874=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2979404	NM_001303256.3(MORC2):c.1304A>T (p.Glu435Val)	MORC2 (E373V +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2975234	NM_001303256.3(MORC2):c.227-16G>T	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2973164	NM_001303256.3(MORC2):c.398C>T (p.Thr133Met)	MORC2 (T71M +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2973005	NM_001303256.3(MORC2):c.462C>A (p.Thr154=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2971929	NM_001303256.3(MORC2):c.2405G>A (p.Arg802His)	MORC2 (R740H +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2970391	NM_001303256.3(MORC2):c.2134C>T (p.Pro712Ser)	MORC2 (P712S +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2968756	NM_001303256.3(MORC2):c.326T>C (p.Met109Thr)	MORC2 (M109T +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2963236	NM_001303256.3(MORC2):c.160A>G (p.Arg54Gly)	MORC2 (R54G)	Single nucleotide variant (missense variant +1 more)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2962922	NM_001303256.3(MORC2):c.1828C>T (p.Pro610Ser)	MORC2 (P548S +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2961848	NM_001303256.3(MORC2):c.2443G>T (p.Val815Leu)	MORC2 (V815L +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2960752	NM_001303256.3(MORC2):c.1074-7T>G	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2960476	NM_001303256.3(MORC2):c.1501T>C (p.Leu501=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2955060	NM_001303256.3(MORC2):c.904+19C>T	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2954926	NM_001303256.3(MORC2):c.1191G>A (p.Val397=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2920252	NM_001303256.3(MORC2):c.2968A>C (p.Thr990Pro)	MORC2 (T928P +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2914252	NM_001303256.3(MORC2):c.2522+12A>G	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2910880	NM_001303256.3(MORC2):c.2950G>A (p.Glu984Lys)	MORC2 (E922K +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2910311	NM_001303256.3(MORC2):c.2381-19C>T	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2909608	NM_001303256.3(MORC2):c.2535C>A (p.Gly845=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2908520	NM_001303256.3(MORC2):c.1804T>A (p.Ser602Thr)	MORC2 (S602T +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2908486	NM_001303256.3(MORC2):c.2852T>G (p.Phe951Cys)	MORC2 (F889C +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2905827	NM_001303256.3(MORC2):c.158-5T>A	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2903740	NM_001303256.3(MORC2):c.2730G>C (p.Leu910=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2903677	NM_001303256.3(MORC2):c.1073+15T>C	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2901120	NM_001303256.3(MORC2):c.825-8C>T	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2899276	NM_001303256.3(MORC2):c.269G>A (p.Arg90Gln)	MORC2 (R28Q +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2896436	NM_001303256.3(MORC2):c.1586C>A (p.Pro529His)	MORC2 (P529H +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2893690	NM_001303256.3(MORC2):c.441G>A (p.Leu147=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2891352	NM_001303256.3(MORC2):c.3031-19C>T	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2888469	NM_001303256.3(MORC2):c.2431C>T (p.Arg811Cys)	MORC2 (R749C +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2877037	NM_001303256.3(MORC2):c.603C>T (p.Ile201=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2873794	NM_001303256.3(MORC2):c.3064G>A (p.Ala1022Thr)	MORC2 (A1019T +2 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2871458	NM_001303256.3(MORC2):c.1370-19A>T	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2867062	NM_001303256.3(MORC2):c.1074-20G>C	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2866815	NM_001303256.3(MORC2):c.68+16G>C	MORC2	Single nucleotide variant (5 prime UTR variant +1 more)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2864528	NM_001303256.3(MORC2):c.2023C>G (p.Arg675Gly)	MORC2 (R675G +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2862944	NM_001303256.3(MORC2):c.1186A>G (p.Lys396Glu)	MORC2 (K334E +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2861762	NM_001303256.3(MORC2):c.3030+19C>G	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2860884	NM_001303256.3(MORC2):c.69-9T>A	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2859354	NM_001303256.3(MORC2):c.3082A>G (p.Ile1028Val)	MORC2 (I1028V +2 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2856706	NM_001303256.3(MORC2):c.3008C>T (p.Ala1003Val)	MORC2 (A941V +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2856587	NM_001303256.3(MORC2):c.480C>A (p.Asp160Glu)	MORC2 (D160E +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2853116	NM_001303256.3(MORC2):c.2265G>A (p.Arg755=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2846476	NM_001303256.3(MORC2):c.587-3C>T	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2839811	NM_001303256.3(MORC2):c.991A>G (p.Met331Val)	MORC2 (M269V +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2839732	NM_001303256.3(MORC2):c.95_96delinsGT (p.Ala32Gly)	MORC2 (A32G)	Indel (missense variant +1 more)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2839658	NM_001303256.3(MORC2):c.2433T>C (p.Arg811=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2834679	NM_001303256.3(MORC2):c.2379A>C (p.Lys793Asn)	MORC2 (K731N +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2833312	NM_001303256.3(MORC2):c.1140T>C (p.Asp380=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2827342	NM_001303256.3(MORC2):c.2747G>A (p.Arg916Gln)	MORC2 (R854Q +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2824927	NM_001303256.3(MORC2):c.1960C>T (p.Pro654Ser)	MORC2 (P592S +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2822633	NM_001303256.3(MORC2):c.2122G>A (p.Glu708Lys)	MORC2 (E708K +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2817916	NM_001303256.3(MORC2):c.1737+8G>A	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2816781	NM_001303256.3(MORC2):c.219G>A (p.Met73Ile)	MORC2 (M73I +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2815570	NM_001303256.3(MORC2):c.988G>T (p.Val330Leu)	MORC2 (V330L +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2810254	NM_001303256.3(MORC2):c.1271C>A (p.Thr424Lys)	MORC2 (T362K +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely pathogenic
Select item 2805120	NM_001303256.3(MORC2):c.226+10G>A	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2803391	NM_001303256.3(MORC2):c.1605-20G>A	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2801030	NM_001303256.3(MORC2):c.1506T>C (p.Cys502=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2796449	NM_001303256.3(MORC2):c.1812+17T>G	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2791852	NM_001303256.3(MORC2):c.765C>T (p.Ile255=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2790685	NM_001303256.3(MORC2):c.284C>T (p.Thr95Ile)	MORC2 (T95I +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2789248	NM_001303256.3(MORC2):c.2912C>T (p.Ser971Phe)	MORC2 (S909F +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2783368	NM_001303256.3(MORC2):c.2738A>G (p.Gln913Arg)	MORC2 (Q913R +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2782359	NM_001303256.3(MORC2):c.560A>T (p.Gln187Leu)	MORC2 (Q125L +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2781029	NM_001303256.3(MORC2):c.904+15G>A	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2780820	NM_001303256.3(MORC2):c.2380+16G>A	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2766221	NM_001303256.3(MORC2):c.223C>T (p.Pro75Ser)	MORC2 (P13S +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2756567	NM_001303256.3(MORC2):c.16T>G (p.Tyr6Asp)	MORC2 (Y6D)	Single nucleotide variant (missense variant +1 more)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2755163	NM_001303256.3(MORC2):c.2381-8A>G	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2749315	NM_001303256.3(MORC2):c.318G>A (p.Ser106=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z +1 more	GUncertain significance
Select item 2741320	NM_001303256.3(MORC2):c.1215-8C>T	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2740036	NM_001303256.3(MORC2):c.69-19T>G	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2737036	NM_001303256.3(MORC2):c.1271C>G (p.Thr424Arg)	MORC2 (T362R +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GPathogenic
Select item 2735641	NM_001303256.3(MORC2):c.2326-12C>T	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2733495	NM_001303256.3(MORC2):c.2619G>A (p.Val873=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2732507	NM_001303256.3(MORC2):c.1498+15T>C	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2731481	NM_001303256.3(MORC2):c.2508A>G (p.Thr836=)	MORC2	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2730177	NM_001303256.3(MORC2):c.987+19C>A	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2729977	NM_001303256.3(MORC2):c.2326-11T>A	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 2727912	NM_001303256.3(MORC2):c.2326-10C>G	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2727770	NM_001303256.3(MORC2):c.2523-21_2523-20del	MORC2	Deletion (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GLikely benign
Select item 2727316	NM_001303256.3(MORC2):c.2213G>A (p.Arg738Gln)	MORC2 (R676Q +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance

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