ClinVar for Gene (Select 10667) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3277725	NM_006567.5(FARS2):c.310C>A (p.Arg104Ser)	FARS2, LOC126859565 (R104S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3277724	NM_006567.5(FARS2):c.753G>A (p.Met251Ile)	FARS2 (M19I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3256857	NM_006567.5(FARS2):c.904+555A>G	FARS2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 3256845	NM_006567.5(FARS2):c.904+14334C>T	FARS2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 3256817	NM_006567.5(FARS2):c.1217+6135A>G	FARS2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 3256802	NM_006567.5(FARS2):c.1217+37690T>C	FARS2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 3246036	NC_000006.11:g.(?_5404755)_(5613573_?)dup	FARS2	Duplication	Combined oxidative phosphorylation defect type 14	GLikely pathogenic
Select item 3246035	NC_000006.11:g.(?_5545393)_(5613573_?)del	FARS2	Deletion	Combined oxidative phosphorylation defect type 14	GPathogenic
Select item 3246034	NC_000006.12:g.(?_5613149)_(5613340_?)del	FARS2	Deletion	Combined oxidative phosphorylation defect type 14	GPathogenic
Select item 3246032	NC_000006.11:g.(?_5109657)_(5771662_?)del	FARS2, LYRM4	Deletion	Combined oxidative phosphorylation defect type 14	GPathogenic
Select item 3121718	NM_020408.6(LYRM4):c.63G>C (p.Lys21Asn)	FARS2, LOC129995672 +1 more (K21N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3092908	NM_006567.5(FARS2):c.395C>T (p.Pro132Leu)	FARS2, LOC126859565 (P132L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3092907	NM_006567.5(FARS2):c.362C>A (p.Thr121Lys)	FARS2, LOC126859565 (T121K)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3092906	NM_006567.5(FARS2):c.1169G>A (p.Gly390Glu)	FARS2 (G158E +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3063625	NC_000006.11:g.(5261894_5368782)_(5545574_5613401)dup	FARS2	Duplication	not specified	GUncertain significance
Select item 3062919	GRCh37/hg19 6p25.1(chr6:5200686-5396374)x1	FARS2, LYRM4	Copy number loss	not specified	GUncertain significance
Select item 3062905	GRCh37/hg19 6p25.1(chr6:5216289-5316709)x1	FARS2, LYRM4	Copy number loss	not specified	GUncertain significance
Select item 3013773	NM_006567.5(FARS2):c.442C>T (p.Arg148Trp)	FARS2, LOC126859565 (R148W)	Single nucleotide variant (missense variant +1 more)	Combined oxidative phosphorylation defect type 14	GUncertain significance
Select item 3004816	NM_006567.5(FARS2):c.333G>C (p.Ser111=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2996339	NM_006567.5(FARS2):c.486C>T (p.Asp162=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2986631	NM_006567.5(FARS2):c.108T>C (p.Pro36=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2964974	NM_006567.5(FARS2):c.613-18T>C	FARS2	Single nucleotide variant (intron variant)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2919338	NM_006567.5(FARS2):c.846T>C (p.His282=)	FARS2	Single nucleotide variant (synonymous variant +1 more)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2912666	NM_006567.5(FARS2):c.555C>T (p.Ser185=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2911891	NM_006567.5(FARS2):c.829A>G (p.Met277Val)	FARS2 (M45V +1 more)	Single nucleotide variant (missense variant +1 more)	Combined oxidative phosphorylation defect type 14	GBenign
Select item 2898667	NM_006567.5(FARS2):c.651C>G (p.Leu217=)	FARS2	Single nucleotide variant (synonymous variant +1 more)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2891865	NM_006567.5(FARS2):c.726T>C (p.Asp242=)	FARS2	Single nucleotide variant (synonymous variant)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2883507	NM_006567.5(FARS2):c.772+7G>A	FARS2	Single nucleotide variant (intron variant)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2874939	NM_006567.5(FARS2):c.925G>C (p.Gly309Arg)	FARS2 (G265R +2 more)	Single nucleotide variant (missense variant)	Combined oxidative phosphorylation defect type 14	GLikely pathogenic
Select item 2871305	NM_006567.5(FARS2):c.1066-5G>T	FARS2	Single nucleotide variant (intron variant)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2870316	NM_006567.5(FARS2):c.475C>T (p.His159Tyr)	FARS2, LOC126859565 (H159Y)	Single nucleotide variant (missense variant +1 more)	Combined oxidative phosphorylation defect type 14	GUncertain significance
Select item 2861363	NM_006567.5(FARS2):c.11C>G (p.Ser4Ter)	FARS2, LOC126859565 (S4*)	Single nucleotide variant (nonsense +1 more)	Combined oxidative phosphorylation defect type 14	GPathogenic
Select item 2853810	NM_006567.5(FARS2):c.1267C>A (p.Arg423=)	FARS2	Single nucleotide variant (synonymous variant)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2851733	NM_006567.5(FARS2):c.597C>G (p.Leu199=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2841126	NM_006567.5(FARS2):c.904+11A>T	FARS2	Single nucleotide variant (intron variant)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2832641	NM_006567.5(FARS2):c.613-15C>A	FARS2	Single nucleotide variant (intron variant)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2818571	NM_006567.5(FARS2):c.768A>G (p.Gly256=)	FARS2	Single nucleotide variant (synonymous variant)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2817319	NM_006567.5(FARS2):c.262C>T (p.Leu88=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2805964	NM_006567.5(FARS2):c.804C>T (p.Phe268=)	FARS2	Single nucleotide variant (synonymous variant +1 more)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2802988	NM_006567.5(FARS2):c.513C>T (p.Phe171=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2797618	NM_006567.5(FARS2):c.528T>C (p.Asp176=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2796234	NM_006567.5(FARS2):c.613-9G>C	FARS2	Single nucleotide variant (intron variant)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2789695	NM_006567.5(FARS2):c.613-13T>C	FARS2	Single nucleotide variant (intron variant)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2788828	NM_006567.5(FARS2):c.234G>T (p.Leu78=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2771426	NM_006567.5(FARS2):c.1218-73_1289delinsC	FARS2	Indel (splice acceptor variant)	Combined oxidative phosphorylation defect type 14	GPathogenic
Select item 2749541	NM_006567.5(FARS2):c.1126T>C (p.Tyr376His)	FARS2 (Y376H +2 more)	Single nucleotide variant (missense variant)	Combined oxidative phosphorylation defect type 14	GUncertain significance
Select item 2746945	NM_006567.5(FARS2):c.613-10T>G	FARS2	Single nucleotide variant (intron variant)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2741020	NM_006567.5(FARS2):c.1154T>C (p.Val385Ala)	FARS2 (V385A +2 more)	Single nucleotide variant (missense variant)	Combined oxidative phosphorylation defect type 14	GUncertain significance
Select item 2740894	NM_006567.5(FARS2):c.772+11A>T	FARS2	Single nucleotide variant (intron variant)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2694983	NM_006567.5(FARS2):c.294C>T (p.Tyr98=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2691634	NC_000006.11:g.(?_5261745)_(5545574_5613401)del	FARS2	Deletion	FARS2-related disorder	GPathogenic
Select item 2684439	GRCh37/hg19 6p25.3-22.3(chr6:156975-15478095)x3	ADTRP, BLOC1S5 +73 more	Copy number gain	not provided	GPathogenic
Select item 2674635	NM_006567.5(FARS2):c.593G>T (p.Arg198Leu)	FARS2 (R198L)	Single nucleotide variant (missense variant +1 more)	Combined oxidative phosphorylation defect type 14	GPathogenic
Select item 2674634	NM_006567.5:c.(?_-4)_(612+185_613-1)del	FARS2	Deletion	Combined oxidative phosphorylation defect type 14	GPathogenic
Select item 2656195	NM_006567.5(FARS2):c.228G>A (p.Arg76=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2629582	NM_006567.5(FARS2):c.509C>T (p.Ala170Val)	FARS2, LOC126859565 (A170V)	Single nucleotide variant (missense variant +1 more)	FARS2-related disorder	GUncertain significance
Select item 2582506	NM_006567.5(FARS2):c.1345G>C (p.Gly449Arg)	FARS2 (G217R +2 more)	Single nucleotide variant (missense variant)	Combined oxidative phosphorylation defect type 14	GUncertain significance
Select item 2578453	NM_006567.5(FARS2):c.862G>C (p.Val288Leu)	FARS2 (V288L +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary spastic paraplegia 77	GUncertain significance
Select item 2576035	NM_006567.5(FARS2):c.1218-33495A>G	FARS2	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2576034	NM_006567.5(FARS2):c.1065+9040A>G	FARS2	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2576033	NM_006567.5(FARS2):c.1217+75319G>C	FARS2, LOC101927950	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2574986	NM_006567.5(FARS2):c.187C>A (p.His63Asn)	FARS2, LOC126859565 (H63N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2500183	NC_000006.11:g.(?_5172693)_(5459957_?)del	FARS2, LYRM4	Deletion	Combined oxidative phosphorylation defect type 14	GPathogenic
Select item 2425615	NC_000006.11:g.(?_5771504)_(6182394_?)dup	F13A1, FARS2 +1 more	Duplication	Combined oxidative phosphorylation defect type 14	GUncertain significance
Select item 2425614	NC_000006.11:g.(?_5216831)_(5431425_?)del	FARS2, LYRM4	Deletion	Combined oxidative phosphorylation defect type 14	GPathogenic
Select item 2425613	NC_000006.11:g.(?_5368804)_(5369435_?)del	FARS2	Deletion	Combined oxidative phosphorylation defect type 14	GPathogenic
Select item 2425612	NC_000006.11:g.(?_5109657)_(6320826_?)del	F13A1, FARS2 +2 more	Deletion	Combined oxidative phosphorylation defect type 14	GPathogenic
Select item 2425611	NC_000006.11:g.(?_5368804)_(5613573_?)dup	FARS2	Duplication	Combined oxidative phosphorylation defect type 14	GUncertain significance
Select item 2425610	NC_000006.11:g.(?_5368804)_(5404954_?)dup	FARS2	Duplication	Combined oxidative phosphorylation defect type 14	GUncertain significance
Select item 2425609	NC_000006.11:g.(?_5545393)_(5545593_?)dup	FARS2	Duplication	Combined oxidative phosphorylation defect type 14	GLikely pathogenic
Select item 2425608	NC_000006.11:g.(?_5404755)_(5404954_?)dup	FARS2	Duplication	Combined oxidative phosphorylation defect type 14	GLikely pathogenic
Select item 2425607	NC_000006.11:g.(?_5404755)_(5545593_?)del	FARS2	Deletion	Combined oxidative phosphorylation defect type 14	GPathogenic
Select item 2425606	NC_000006.11:g.(?_5404755)_(5431425_?)del	FARS2	Deletion	Combined oxidative phosphorylation defect type 14	GPathogenic
Select item 2425605	NC_000006.11:g.(?_5368804)_(5404954_?)del	FARS2	Deletion	Combined oxidative phosphorylation defect type 14	GPathogenic
Select item 2402657	NM_020408.6(LYRM4):c.40C>T (p.Arg14Trp)	FARS2, LOC129995672 +1 more (R14W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402656	NM_020408.6(LYRM4):c.34C>G (p.Leu12Val)	FARS2, LOC129995672 +1 more (L12V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2325902	NM_006567.5(FARS2):c.754G>C (p.Ala252Pro)	FARS2 (A252P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2320667	NM_006567.5(FARS2):c.892C>G (p.Leu298Val)	FARS2 (L298V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2295113	NM_006567.5(FARS2):c.1235A>G (p.His412Arg)	FARS2 (H180R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2256868	NM_006567.5(FARS2):c.758A>G (p.His253Arg)	FARS2 (H253R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2232075	NM_006567.5(FARS2):c.697A>G (p.Met233Val)	FARS2 (M1V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2230519	NM_006567.5(FARS2):c.773-6T>A	FARS2	Single nucleotide variant (intron variant)	Inborn genetic diseases	GUncertain significance
Select item 2202486	NM_006567.5(FARS2):c.1168_1173del (p.Gly390_Asp391del)	FARS2	Deletion (inframe_deletion)	not specified +1 more	GUncertain significance
Select item 2191367	NM_006567.5(FARS2):c.284A>G (p.Glu95Gly)	FARS2, LOC126859565 (E95G)	Single nucleotide variant (missense variant +1 more)	Combined oxidative phosphorylation defect type 14	GUncertain significance
Select item 2190012	NM_006567.5(FARS2):c.261G>C (p.Trp87Cys)	FARS2, LOC126859565 (W87C)	Single nucleotide variant (missense variant +1 more)	Combined oxidative phosphorylation defect type 14	GUncertain significance
Select item 2175037	NM_006567.5(FARS2):c.772+4A>G	FARS2	Single nucleotide variant (intron variant)	Combined oxidative phosphorylation defect type 14	GUncertain significance
Select item 2172251	NM_006567.5(FARS2):c.453G>A (p.Met151Ile)	FARS2, LOC126859565 (M151I)	Single nucleotide variant (missense variant +1 more)	Combined oxidative phosphorylation defect type 14	GUncertain significance
Select item 2169416	NM_006567.5(FARS2):c.1262T>C (p.Met421Thr)	FARS2 (M189T +2 more)	Single nucleotide variant (missense variant)	Combined oxidative phosphorylation defect type 14	GUncertain significance
Select item 2163232	NM_006567.5(FARS2):c.773-7T>C	FARS2	Single nucleotide variant (intron variant)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2148796	NM_020408.6(LYRM4):c.75C>T (p.Ala25=)	FARS2, LOC129995672 +1 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2141364	NM_006567.5(FARS2):c.772+20T>C	FARS2	Single nucleotide variant (intron variant)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2134155	NM_006567.5(FARS2):c.1110G>A (p.Trp370Ter)	FARS2 (W370* +2 more)	Single nucleotide variant (nonsense)	Combined oxidative phosphorylation defect type 14	GPathogenic
Select item 2130378	NM_006567.5(FARS2):c.1093A>C (p.Asn365His)	FARS2 (N133H +2 more)	Single nucleotide variant (missense variant)	Combined oxidative phosphorylation defect type 14	GUncertain significance
Select item 2127422	NM_006567.5(FARS2):c.999G>T (p.Trp333Cys)	FARS2 (W289C +2 more)	Single nucleotide variant (missense variant)	Combined oxidative phosphorylation defect type 14	GUncertain significance
Select item 2123634	NM_006567.5(FARS2):c.904+16A>G	FARS2	Single nucleotide variant (intron variant)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2121091	NM_006567.5(FARS2):c.1066-17T>C	FARS2	Single nucleotide variant (intron variant)	Combined oxidative phosphorylation defect type 14	GLikely benign
Select item 2104661	NM_006567.5(FARS2):c.178C>T (p.Gln60Ter)	FARS2, LOC126859565 (Q60*)	Single nucleotide variant (nonsense +1 more)	Combined oxidative phosphorylation defect type 14	GPathogenic
Select item 2092976	NM_006567.5(FARS2):c.497dup (p.Leu168fs)	FARS2, LOC126859565 (L168fs)	Duplication (frameshift variant +1 more)	Combined oxidative phosphorylation defect type 14	GPathogenic
Select item 2091606	NM_006567.5(FARS2):c.388C>T (p.Leu130Phe)	FARS2, LOC126859565 (L130F)	Single nucleotide variant (missense variant +1 more)	Combined oxidative phosphorylation defect type 14	GUncertain significance
Select item 2086226	NM_006567.5(FARS2):c.474A>T (p.Ala158=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	Combined oxidative phosphorylation defect type 14	GLikely benign

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