"PreventionGenetics, part of Exact Sciences"[submitter] AND "MYOM2"[ge - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3041015	NM_003970.4(MYOM2):c.-6G>A	MYOM2	Single nucleotide variant (5 prime UTR variant)	MYOM2-related condition	GLikely benign
Select item 3050181	NM_003970.4(MYOM2):c.57C>T (p.Ser19=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GLikely benign
Select item 3060228	NM_003970.4(MYOM2):c.98C>A (p.Ala33Glu)	MYOM2 (A33E)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3056560	NM_003970.4(MYOM2):c.241G>A (p.Glu81Lys)	MYOM2 (E81K)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3060195	NM_003970.4(MYOM2):c.260G>T (p.Ser87Ile)	MYOM2 (S87I)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3057963	NM_003970.4(MYOM2):c.263+6C>T	MYOM2	Single nucleotide variant (intron variant)	MYOM2-related condition	GLikely benign
Select item 3033344	NM_003970.4(MYOM2):c.367C>T (p.Arg123Cys)	MYOM2 (R123C)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3042957	NM_003970.4(MYOM2):c.370G>A (p.Asp124Asn)	MYOM2 (D124N)	Single nucleotide variant (missense variant)	MYOM2-related condition	GLikely benign
Select item 2658306	NM_003970.4(MYOM2):c.389C>G (p.Ala130Gly)	MYOM2 (A130G)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3050784	NM_003970.4(MYOM2):c.408G>A (p.Glu136=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GLikely benign
Select item 3037217	NM_003970.4(MYOM2):c.475C>T (p.Arg159Trp)	MYOM2 (R159W)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3056138	NM_003970.4(MYOM2):c.545C>T (p.Thr182Met)	MYOM2 (T182M)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3045572	NM_003970.4(MYOM2):c.550G>A (p.Val184Met)	MYOM2 (V184M)	Single nucleotide variant (missense variant)	MYOM2-related condition	GLikely benign
Select item 3038323	NM_003970.4(MYOM2):c.590C>T (p.Ala197Val)	MYOM2 (A197V)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3050175	NM_003970.4(MYOM2):c.600G>A (p.Pro200=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GLikely benign
Select item 3042223	NM_003970.4(MYOM2):c.623A>G (p.Asn208Ser)	MYOM2 (N208S)	Single nucleotide variant (missense variant)	MYOM2-related condition	GLikely benign
Select item 3049311	NM_003970.4(MYOM2):c.654-9C>T	MYOM2	Single nucleotide variant (intron variant)	MYOM2-related condition	GBenign
Select item 3055406	NM_003970.4(MYOM2):c.656C>T (p.Ala219Val)	MYOM2 (A219V)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3056775	NM_003970.4(MYOM2):c.672T>C (p.Thr224=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3044667	NM_003970.4(MYOM2):c.783C>G (p.Leu261=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GLikely benign
Select item 3060807	NM_003970.4(MYOM2):c.794-47_794-8dup	MYOM2	Duplication (intron variant)	MYOM2-related condition	GLikely benign
Select item 3043288	NM_003970.4(MYOM2):c.876C>T (p.Gly292=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3042626	NM_003970.4(MYOM2):c.882G>A (p.Thr294=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GLikely benign
Select item 2658307	NM_003970.4(MYOM2):c.911C>T (p.Thr304Met)	MYOM2 (T304M)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 3060470	NM_003970.4(MYOM2):c.961G>T (p.Val321Leu)	MYOM2 (V321L)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3037866	NM_003970.4(MYOM2):c.1087G>A (p.Val363Ile)	MYOM2 (V363I)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3056904	NM_003970.4(MYOM2):c.1180G>A (p.Ala394Thr)	MYOM2 (A394T)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3043704	NM_003970.4(MYOM2):c.1216C>T (p.Pro406Ser)	MYOM2 (P406S)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 2658308	NM_003970.4(MYOM2):c.1308G>C (p.Pro436=)	MYOM2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3034385	NM_003970.4(MYOM2):c.1398C>G (p.Ser466Arg)	MYOM2 (S466R)	Single nucleotide variant (missense variant)	MYOM2-related condition	GLikely benign
Select item 3060159	NM_003970.4(MYOM2):c.1463-8C>G	MYOM2	Single nucleotide variant (intron variant)	MYOM2-related condition	GBenign
Select item 3040397	NM_003970.4(MYOM2):c.1554C>T (p.His518=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GLikely benign
Select item 3057073	NM_003970.4(MYOM2):c.1568G>A (p.Ser523Asn)	MYOM2 (S523N)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3044008	NM_003970.4(MYOM2):c.1581C>T (p.Val527=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3050437	NM_003970.4(MYOM2):c.1617G>C (p.Lys539Asn)	MYOM2 (K539N)	Single nucleotide variant (missense variant)	MYOM2-related condition	GLikely benign
Select item 3044685	NM_003970.4(MYOM2):c.1622C>T (p.Pro541Leu)	MYOM2 (P541L)	Single nucleotide variant (missense variant)	MYOM2-related condition	GLikely benign
Select item 3045214	NM_003970.4(MYOM2):c.1650G>C (p.Val550=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3044831	NM_003970.4(MYOM2):c.1659C>T (p.Ser553=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GLikely benign
Select item 3037366	NM_003970.4(MYOM2):c.1688C>T (p.Thr563Met)	MYOM2 (T563M)	Single nucleotide variant (missense variant)	MYOM2-related condition	GLikely benign
Select item 3052283	NM_003970.4(MYOM2):c.1786C>A (p.Pro596Thr)	MYOM2 (P596T)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3048516	NM_003970.4(MYOM2):c.1802C>A (p.Ser601Tyr)	MYOM2 (S601Y)	Single nucleotide variant (missense variant)	MYOM2-related condition	GLikely benign
Select item 3038640	NM_003970.4(MYOM2):c.1833C>A (p.Val611=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3055432	NM_003970.4(MYOM2):c.1836T>G (p.Pro612=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3024957	NM_003970.4(MYOM2):c.1943G>A (p.Cys648Tyr)	MYOM2 (C648Y)	Single nucleotide variant (missense variant)	MYOM2-related condition +1 more	GLikely benign
Select item 3060404	NM_003970.4(MYOM2):c.1953C>T (p.Ala651=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3044658	NM_003970.4(MYOM2):c.1993G>A (p.Gly665Arg)	MYOM2 (G665R)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3044971	NM_003970.4(MYOM2):c.2014C>T (p.His672Tyr)	MYOM2 (H672Y)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3056223	NM_003970.4(MYOM2):c.2041A>C (p.Ile681Leu)	MYOM2 (I681L)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3044267	NM_003970.4(MYOM2):c.2067T>C (p.Ala689=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3049262	NM_003970.4(MYOM2):c.2100C>T (p.Asp700=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GLikely benign
Select item 3055552	NM_003970.4(MYOM2):c.2101G>A (p.Val701Ile)	MYOM2 (V701I)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3039360	NM_003970.4(MYOM2):c.2133G>A (p.Pro711=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3038040	NM_003970.4(MYOM2):c.2162A>G (p.Asn721Ser)	MYOM2 (N721S)	Single nucleotide variant (missense variant)	MYOM2-related condition	GLikely benign
Select item 3055965	NM_003970.4(MYOM2):c.2170G>A (p.Gly724Ser)	MYOM2 (G724S)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3038376	NM_003970.4(MYOM2):c.2242G>A (p.Asp748Asn)	MYOM2 (D748N)	Single nucleotide variant (missense variant)	MYOM2-related condition	GLikely benign
Select item 3043808	NM_003970.4(MYOM2):c.2290C>T (p.Pro764Ser)	MYOM2 (P764S)	Single nucleotide variant (missense variant)	MYOM2-related condition	GLikely benign
Select item 3052995	NM_003970.4(MYOM2):c.2319C>T (p.Asp773=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3059885	NM_003970.4(MYOM2):c.2327C>T (p.Thr776Met)	MYOM2 (T776M)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3037853	NM_003970.4(MYOM2):c.2356G>A (p.Ala786Thr)	MYOM2 (A786T)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 2658311	NM_003970.4(MYOM2):c.2358C>T (p.Ala786=)	MYOM2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2215779	NM_003970.4(MYOM2):c.2399G>T (p.Ser800Ile)	MYOM2 (S800I)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3042825	NM_003970.4(MYOM2):c.2460G>A (p.Thr820=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GLikely benign
Select item 3056723	NM_003970.4(MYOM2):c.2682C>T (p.Gly894=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3038320	NM_003970.4(MYOM2):c.2683G>A (p.Val895Met)	MYOM2 (V895M)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3034134	NM_003970.4(MYOM2):c.2727G>A (p.Ala909=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3060055	NM_003970.4(MYOM2):c.2769A>G (p.Gln923=)	LOC126860282, MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3057018	NM_003970.4(MYOM2):c.2780A>G (p.Tyr927Cys)	LOC126860282, MYOM2 (Y927C)	Single nucleotide variant (missense variant)	MYOM2-related condition	GLikely benign
Select item 3049272	NM_003970.4(MYOM2):c.2812G>A (p.Ala938Thr)	LOC126860282, MYOM2 (A938T)	Single nucleotide variant (missense variant)	MYOM2-related condition	GLikely benign
Select item 3039329	NM_003970.4(MYOM2):c.2814G>A (p.Ala938=)	LOC126860282, MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GLikely benign
Select item 3049094	NM_003970.4(MYOM2):c.2861A>G (p.Glu954Gly)	LOC126860282, MYOM2 (E954G)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3049343	NM_003970.4(MYOM2):c.2883G>A (p.Val961=)	LOC126860282, MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GLikely benign
Select item 3038408	NM_003970.4(MYOM2):c.2916G>T (p.Pro972=)	LOC126860282, MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3056801	NM_003970.4(MYOM2):c.2999-8C>T	MYOM2	Single nucleotide variant (intron variant)	MYOM2-related condition	GBenign
Select item 3050335	NM_003970.4(MYOM2):c.3000G>A (p.Glu1000=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GLikely benign
Select item 3049766	NM_003970.4(MYOM2):c.3043+6T>C	MYOM2	Single nucleotide variant (intron variant)	MYOM2-related condition	GLikely benign
Select item 3060768	NM_003970.4(MYOM2):c.3156C>T (p.Asn1052=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 2658312	NM_003970.4(MYOM2):c.3258G>A (p.Gly1086=)	MYOM2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2658313	NM_003970.4(MYOM2):c.3320G>C (p.Gly1107Ala)	MYOM2 (G1107A)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 3056987	NM_003970.4(MYOM2):c.3326-10T>C	MYOM2	Single nucleotide variant (intron variant)	MYOM2-related condition	GLikely benign
Select item 3056396	NM_003970.4(MYOM2):c.3471A>G (p.Lys1157=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3059679	NM_003970.4(MYOM2):c.3503T>C (p.Val1168Ala)	MYOM2 (V1168A)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3060613	NM_003970.4(MYOM2):c.3585C>T (p.His1195=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3059210	NM_003970.4(MYOM2):c.3612T>C (p.Asp1204=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3037726	NM_003970.4(MYOM2):c.3648T>G (p.Ala1216=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3041992	NM_003970.4(MYOM2):c.3655+7G>A	MYOM2	Single nucleotide variant (intron variant)	MYOM2-related condition	GBenign
Select item 3046378	NM_003970.4(MYOM2):c.3694+10T>C	MYOM2	Single nucleotide variant (intron variant)	MYOM2-related condition	GLikely benign
Select item 3054672	NM_003970.4(MYOM2):c.3780G>A (p.Met1260Ile)	MYOM2 (M1260I)	Single nucleotide variant (missense variant)	MYOM2-related condition	GLikely benign
Select item 3041770	NM_003970.4(MYOM2):c.3837C>T (p.Ile1279=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3039151	NM_003970.4(MYOM2):c.3843G>T (p.Gly1281=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3044512	NM_003970.4(MYOM2):c.3852G>C (p.Glu1284Asp)	MYOM2 (E1284D)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3039158	NM_003970.4(MYOM2):c.3858T>C (p.Ala1286=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3038713	NM_003970.4(MYOM2):c.3872G>T (p.Cys1291Phe)	MYOM2 (C1291F)	Single nucleotide variant (missense variant)	MYOM2-related condition	GBenign
Select item 3050063	NM_003970.4(MYOM2):c.3900A>G (p.Lys1300=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GLikely benign
Select item 3038429	NM_003970.4(MYOM2):c.3930C>T (p.Asp1310=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3059199	NM_003970.4(MYOM2):c.3952C>T (p.Leu1318=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3037537	NM_003970.4(MYOM2):c.3993G>A (p.Gln1331=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GLikely benign
Select item 3039564	NM_003970.4(MYOM2):c.3996A>G (p.Gln1332=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3039136	NM_003970.4(MYOM2):c.4056C>T (p.Asp1352=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GBenign
Select item 3035221	NM_003970.4(MYOM2):c.4081-10C>G	MYOM2	Single nucleotide variant (intron variant)	MYOM2-related condition	GLikely benign
Select item 3042131	NM_003970.4(MYOM2):c.4113C>T (p.Asn1371=)	MYOM2	Single nucleotide variant (synonymous variant)	MYOM2-related condition	GLikely benign

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