Related gene-specific medical variations for Gene (Select 23195) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3124669	NM_014611.3(MDN1):c.16721C>T (p.Ala5574Val)	MDN1, MDN1-AS1 (A5574V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124668	NM_014611.3(MDN1):c.16601G>T (p.Arg5534Leu)	MDN1, MDN1-AS1 (R5534L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124667	NM_014611.3(MDN1):c.16334A>G (p.Tyr5445Cys)	MDN1, MDN1-AS1 (Y5445C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124666	NM_014611.3(MDN1):c.16199C>T (p.Thr5400Ile)	MDN1, MDN1-AS1 (T5400I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124665	NM_014611.3(MDN1):c.16000A>G (p.Ile5334Val)	MDN1, MDN1-AS1 (I5334V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124664	NM_014611.3(MDN1):c.15781A>G (p.Thr5261Ala)	MDN1, MDN1-AS1 (T5261A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124663	NM_014611.3(MDN1):c.15701C>A (p.Thr5234Lys)	MDN1, MDN1-AS1 (T5234K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124662	NM_014611.3(MDN1):c.15463A>C (p.Ser5155Arg)	MDN1, MDN1-AS1 (S5155R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124661	NM_014611.3(MDN1):c.15442T>G (p.Phe5148Val)	MDN1, MDN1-AS1 (F5148V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124660	NM_014611.3(MDN1):c.15098G>C (p.Cys5033Ser)	LOC126859739, MDN1 +1 more (C5033S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124659	NM_014611.3(MDN1):c.15049A>G (p.Thr5017Ala)	LOC126859739, MDN1 +1 more (T5017A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124658	NM_014611.3(MDN1):c.14919A>T (p.Glu4973Asp)	LOC126859739, MDN1 +1 more (E4973D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124655	NM_014611.3(MDN1):c.14756G>A (p.Gly4919Asp)	LOC126859739, MDN1 +1 more (G4919D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124654	NM_014611.3(MDN1):c.14747A>T (p.Glu4916Val)	LOC126859739, MDN1 +1 more (E4916V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124653	NM_014611.3(MDN1):c.14362G>A (p.Glu4788Lys)	MDN1, MDN1-AS1 (E4788K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124652	NM_014611.3(MDN1):c.14352G>T (p.Glu4784Asp)	MDN1, MDN1-AS1 (E4784D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3124651	NM_014611.3(MDN1):c.14269G>A (p.Gly4757Arg)	MDN1, MDN1-AS1 (G4757R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124650	NM_014611.3(MDN1):c.14081G>T (p.Gly4694Val)	MDN1, MDN1-AS1 (G4694V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124649	NM_014611.3(MDN1):c.13703C>T (p.Thr4568Ile)	MDN1, MDN1-AS1 (T4568I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124648	NM_014611.3(MDN1):c.13683C>G (p.Asp4561Glu)	MDN1, MDN1-AS1 (D4561E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124645	NM_014611.3(MDN1):c.13482A>C (p.Gln4494His)	MDN1, MDN1-AS1 (Q4494H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124644	NM_014611.3(MDN1):c.13420A>G (p.Met4474Val)	MDN1, MDN1-AS1 (M4474V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3124643	NM_014611.3(MDN1):c.13064A>G (p.Asn4355Ser)	MDN1, MDN1-AS1 (N4355S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124642	NM_014611.3(MDN1):c.12842A>G (p.Asp4281Gly)	MDN1, MDN1-AS1 (D4281G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124639	NM_014611.3(MDN1):c.12788T>G (p.Ile4263Ser)	MDN1, MDN1-AS1 (I4263S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124638	NM_014611.3(MDN1):c.12601G>A (p.Ala4201Thr)	MDN1, MDN1-AS1 (A4201T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124635	NM_014611.3(MDN1):c.11372C>T (p.Ala3791Val)	MDN1, MDN1-AS1 (A3791V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3124634	NM_014611.3(MDN1):c.11317T>C (p.Phe3773Leu)	MDN1, MDN1-AS1 (F3773L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3060847	NM_014611.3(MDN1):c.14349T>G (p.Asp4783Glu)	MDN1, MDN1-AS1 (D4783E)	Single nucleotide variant (missense variant)	MDN1-related disorder	GBenign
Select item 3060739	NM_014611.3(MDN1):c.11381C>G (p.Ala3794Gly)	MDN1, MDN1-AS1 (A3794G)	Single nucleotide variant (non-coding transcript variant +1 more)	MDN1-related disorder	GBenign
Select item 3058944	NM_014611.3(MDN1):c.14970C>T (p.Ala4990=)	LOC126859739, MDN1 +1 more	Single nucleotide variant (synonymous variant)	MDN1-related disorder	GBenign
Select item 3053060	NM_014611.3(MDN1):c.13692C>T (p.Ala4564=)	MDN1, MDN1-AS1	Single nucleotide variant (synonymous variant)	MDN1-related disorder	GLikely benign
Select item 3053003	NM_014611.3(MDN1):c.13491C>T (p.Asp4497=)	MDN1, MDN1-AS1	Single nucleotide variant (synonymous variant)	MDN1-related disorder	GBenign
Select item 3052651	NM_014611.3(MDN1):c.15923T>C (p.Val5308Ala)	MDN1, MDN1-AS1 (V5308A)	Single nucleotide variant (missense variant)	MDN1-related disorder +1 more	GBenign/Likely benign
Select item 3052319	NM_014611.3(MDN1):c.11719+9T>G	MDN1, MDN1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	MDN1-related disorder	GLikely benign
Select item 3051970	NM_014611.3(MDN1):c.15661+10G>A	MDN1, MDN1-AS1	Single nucleotide variant (intron variant)	MDN1-related disorder	GLikely benign
Select item 3050419	NM_014611.3(MDN1):c.12162G>A (p.Leu4054=)	MDN1, MDN1-AS1	Single nucleotide variant (synonymous variant)	MDN1-related disorder	GLikely benign
Select item 3050402	NM_014611.3(MDN1):c.15156C>T (p.Ala5052=)	LOC126859739, MDN1 +1 more	Single nucleotide variant (synonymous variant)	MDN1-related disorder	GLikely benign
Select item 3050023	NM_014611.3(MDN1):c.13601C>G (p.Thr4534Ser)	MDN1, MDN1-AS1 (T4534S)	Single nucleotide variant (missense variant)	MDN1-related disorder	GBenign
Select item 3049604	NM_014611.3(MDN1):c.15714A>G (p.Gln5238=)	MDN1, MDN1-AS1	Single nucleotide variant (synonymous variant)	MDN1-related disorder	GLikely benign
Select item 3048911	NM_014611.3(MDN1):c.14556A>G (p.Gln4852=)	MDN1, MDN1-AS1	Single nucleotide variant (synonymous variant)	MDN1-related disorder	GLikely benign
Select item 3048887	NM_014611.3(MDN1):c.14705A>G (p.Glu4902Gly)	MDN1, MDN1-AS1 (E4902G)	Single nucleotide variant (missense variant)	MDN1-related disorder	GBenign
Select item 3046141	NM_014611.3(MDN1):c.15704A>C (p.Glu5235Ala)	MDN1, MDN1-AS1 (E5235A)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3045922	NM_014611.3(MDN1):c.12420G>A (p.Ser4140=)	MDN1, MDN1-AS1	Single nucleotide variant (synonymous variant)	MDN1-related disorder	GLikely benign
Select item 3045534	NM_014611.3(MDN1):c.14757T>G (p.Gly4919=)	LOC126859739, MDN1 +1 more	Single nucleotide variant (synonymous variant)	MDN1-related disorder	GBenign
Select item 3045290	NM_014611.3(MDN1):c.16459+7T>C	MDN1, MDN1-AS1	Single nucleotide variant (intron variant)	MDN1-related disorder	GBenign
Select item 3044873	NM_014611.3(MDN1):c.11651A>G (p.His3884Arg)	MDN1, MDN1-AS1 (H3884R)	Single nucleotide variant (non-coding transcript variant +1 more)	MDN1-related disorder	GLikely benign
Select item 3044859	NM_014611.3(MDN1):c.14352GGA[1] (p.Glu4786del)	MDN1, MDN1-AS1 (E4786del)	Microsatellite (inframe deletion)	MDN1-related disorder	GLikely benign
Select item 3043443	NM_014611.3(MDN1):c.13711G>A (p.Val4571Met)	MDN1, MDN1-AS1 (V4571M)	Single nucleotide variant (missense variant)	MDN1-related disorder	GLikely benign
Select item 3042533	NM_014611.3(MDN1):c.13982T>C (p.Met4661Thr)	MDN1, MDN1-AS1 (M4661T)	Single nucleotide variant (missense variant)	MDN1-related disorder	GBenign
Select item 3042097	NM_014611.3(MDN1):c.15233C>T (p.Ser5078Leu)	MDN1, MDN1-AS1 (S5078L)	Single nucleotide variant (missense variant)	MDN1-related disorder	GLikely benign
Select item 3041550	NM_014611.3(MDN1):c.12988C>T (p.Pro4330Ser)	MDN1, MDN1-AS1 (P4330S)	Single nucleotide variant (missense variant)	MDN1-related disorder	GBenign
Select item 3039139	NM_014611.3(MDN1):c.14025T>C (p.Tyr4675=)	MDN1, MDN1-AS1	Single nucleotide variant (synonymous variant)	MDN1-related disorder	GLikely benign
Select item 3038976	NM_014611.3(MDN1):c.16335C>T (p.Tyr5445=)	MDN1, MDN1-AS1	Single nucleotide variant (synonymous variant)	MDN1-related disorder	GBenign
Select item 3038801	NM_014611.3(MDN1):c.12499G>A (p.Ala4167Thr)	MDN1, MDN1-AS1 (A4167T)	Single nucleotide variant (missense variant)	MDN1-related disorder	GBenign
Select item 3038537	NM_014611.3(MDN1):c.15378G>A (p.Thr5126=)	MDN1, MDN1-AS1	Single nucleotide variant (synonymous variant)	MDN1-related disorder	GLikely benign
Select item 3038183	NM_014611.3(MDN1):c.14648A>G (p.Asp4883Gly)	MDN1, MDN1-AS1 (D4883G)	Single nucleotide variant (missense variant)	MDN1-related disorder	GBenign
Select item 3038084	NM_014611.3(MDN1):c.14349TGAGGAGGAAGA[1] (p.4783DEEE[1])	MDN1, MDN1-AS1	Microsatellite (inframe deletion)	MDN1-related disorder	GLikely benign
Select item 3035639	NM_014611.3(MDN1):c.12357T>G (p.Ile4119Met)	MDN1, MDN1-AS1 (I4119M)	Single nucleotide variant (missense variant)	MDN1-related disorder	GBenign
Select item 3034769	NM_014611.3(MDN1):c.13395T>C (p.Tyr4465=)	MDN1, MDN1-AS1	Single nucleotide variant (synonymous variant)	MDN1-related disorder	GLikely benign
Select item 3034416	NM_014611.3(MDN1):c.16031+7C>T	MDN1, MDN1-AS1	Single nucleotide variant (intron variant)	MDN1-related disorder	GLikely benign
Select item 3033690	NM_014611.3(MDN1):c.12646-6T>C	MDN1, MDN1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	MDN1-related disorder	GLikely benign
Select item 2656764	NM_014611.3(MDN1):c.13032T>C (p.Leu4344=)	MDN1, MDN1-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656763	NM_014611.3(MDN1):c.13201G>A (p.Val4401Ile)	MDN1, MDN1-AS1 (V4401I)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2618859	NM_014611.3(MDN1):c.13778C>T (p.Thr4593Ile)	MDN1, MDN1-AS1 (T4593I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609454	NM_014611.3(MDN1):c.14520T>G (p.Asp4840Glu)	MDN1, MDN1-AS1 (D4840E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607934	NM_014611.3(MDN1):c.12865C>T (p.Arg4289Cys)	MDN1, MDN1-AS1 (R4289C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605550	NM_014611.3(MDN1):c.13405G>A (p.Glu4469Lys)	MDN1, MDN1-AS1 (E4469K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600295	NM_014611.3(MDN1):c.11957G>A (p.Arg3986Gln)	MDN1, MDN1-AS1 (R3986Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589676	NM_014611.3(MDN1):c.15139A>G (p.Met5047Val)	LOC126859739, MDN1 +1 more (M5047V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2569289	NM_014611.3(MDN1):c.11208G>T (p.Glu3736Asp)	MDN1, MDN1-AS1 (E3736D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2558682	NM_014611.3(MDN1):c.13120C>T (p.Arg4374Trp)	MDN1, MDN1-AS1 (R4374W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557873	NM_014611.3(MDN1):c.13073A>C (p.Tyr4358Ser)	MDN1, MDN1-AS1 (Y4358S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555608	NM_014611.3(MDN1):c.13546C>A (p.Leu4516Ile)	MDN1, MDN1-AS1 (L4516I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552316	NM_014611.3(MDN1):c.15196G>A (p.Gly5066Arg)	MDN1, MDN1-AS1 (G5066R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552315	NM_014611.3(MDN1):c.11707G>A (p.Val3903Ile)	MDN1, MDN1-AS1 (V3903I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2544501	NM_014611.3(MDN1):c.15281C>G (p.Thr5094Arg)	MDN1, MDN1-AS1 (T5094R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542266	NM_014611.3(MDN1):c.15893G>A (p.Arg5298His)	MDN1, MDN1-AS1 (R5298H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2538254	NM_014611.3(MDN1):c.13114C>T (p.Arg4372Trp)	MDN1, MDN1-AS1 (R4372W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527150	NM_014611.3(MDN1):c.15396G>C (p.Gln5132His)	MDN1, MDN1-AS1 (Q5132H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523903	NM_014611.3(MDN1):c.14201A>C (p.Asp4734Ala)	MDN1, MDN1-AS1 (D4734A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517687	NM_014611.3(MDN1):c.15109G>A (p.Gly5037Ser)	LOC126859739, MDN1 +1 more (G5037S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512869	NM_014611.3(MDN1):c.12308T>C (p.Val4103Ala)	MDN1, MDN1-AS1 (V4103A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486333	NM_014611.3(MDN1):c.12836C>G (p.Pro4279Arg)	MDN1, MDN1-AS1 (P4279R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478065	NM_014611.3(MDN1):c.14542A>G (p.Lys4848Glu)	MDN1, MDN1-AS1 (K4848E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473028	NM_014611.3(MDN1):c.12605G>A (p.Arg4202Gln)	MDN1, MDN1-AS1 (R4202Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458840	NM_014611.3(MDN1):c.12704T>A (p.Met4235Lys)	MDN1, MDN1-AS1 (M4235K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2412352	NM_014611.3(MDN1):c.11525A>G (p.Tyr3842Cys)	MDN1, MDN1-AS1 (Y3842C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2410507	NM_014611.3(MDN1):c.12443C>T (p.Ala4148Val)	MDN1, MDN1-AS1 (A4148V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408564	NM_014611.3(MDN1):c.12713G>A (p.Arg4238Gln)	MDN1, MDN1-AS1 (R4238Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2407277	NM_014611.3(MDN1):c.14973T>G (p.Asp4991Glu)	LOC126859739, MDN1 +1 more (D4991E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404893	NM_014611.3(MDN1):c.12949G>C (p.Ala4317Pro)	MDN1, MDN1-AS1 (A4317P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394469	NM_014611.3(MDN1):c.12286A>G (p.Ser4096Gly)	MDN1, MDN1-AS1 (S4096G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391375	NM_014611.3(MDN1):c.12419C>T (p.Ser4140Leu)	MDN1, MDN1-AS1 (S4140L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391351	NM_014611.3(MDN1):c.12709G>A (p.Val4237Ile)	MDN1, MDN1-AS1 (V4237I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2383350	NM_014611.3(MDN1):c.11485C>T (p.Arg3829Cys)	MDN1, MDN1-AS1 (R3829C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2382557	NM_014611.3(MDN1):c.11470G>C (p.Asp3824His)	MDN1, MDN1-AS1 (D3824H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2375570	NM_014611.3(MDN1):c.16720G>A (p.Ala5574Thr)	MDN1, MDN1-AS1 (A5574T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371004	NM_014611.3(MDN1):c.14300A>G (p.Asn4767Ser)	MDN1, MDN1-AS1 (N4767S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370201	NM_014611.3(MDN1):c.12337C>T (p.Arg4113Trp)	MDN1, MDN1-AS1 (R4113W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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