C4551995[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 21316	NM_002693.3(POLG):c.3708G>T (p.Gln1236His)	FANCI, POLG (Q1236H)	Single nucleotide variant (missense variant +1 more)	not provided +12 more	GBenign/Likely benign
Select item 458718	NM_002693.3(POLG):c.3667A>G (p.Ile1223Val)	FANCI, POLG (I1223V)	Single nucleotide variant (missense variant +1 more)	not specified +9 more	GConflicting classifications of pathogenicity
Select item 206575	NM_002693.3(POLG):c.3650C>T (p.Ala1217Val)	FANCI, POLG (A1217V)	Single nucleotide variant (missense variant +1 more)	Progressive sclerosing poliodystrophy +9 more	GUncertain significance
Select item 597808	NM_002693.3(POLG):c.3643+2T>C	POLG	Single nucleotide variant (splice donor variant)	Mitochondrial disease	GPathogenic FDA Recognized database
Select item 594667	NM_002693.3(POLG):c.3560G>A (p.Arg1187Gln)	POLG (R1187Q)	Single nucleotide variant (missense variant)	not provided +6 more	GUncertain significance
Select item 1418532	NM_002693.3(POLG):c.3532G>A (p.Ala1178Thr)	POLG (A1178T)	Single nucleotide variant (missense variant)	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis +5 more	GUncertain significance
Select item 206568	NM_002693.3(POLG):c.3505G>A (p.Gly1169Ser)	POLG (G1169S)	Single nucleotide variant (missense variant)	POLG-related disorder +7 more	GUncertain significance
Select item 458715	NM_002693.3(POLG):c.3442C>T (p.Arg1148Cys)	POLG (R1148C)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +7 more	GUncertain significance
Select item 21312	NM_002693.3(POLG):c.3428A>G (p.Glu1143Gly)	FANCI, POLG (E1143G)	Single nucleotide variant (missense variant)	Mitochondrial disease	GBenign FDA Recognized database
Select item 195591	NM_002693.3(POLG):c.3425G>A (p.Arg1142Gln)	POLG (R1142Q)	Single nucleotide variant (missense variant)	not provided +6 more	GUncertain significance
Select item 522129	NM_002693.3(POLG):c.3317T>C (p.Val1106Ala)	POLG (V1106A)	Single nucleotide variant (missense variant)	Inborn genetic diseases +7 more	GConflicting classifications of pathogenicity
Select item 206556	NM_002693.3(POLG):c.3286C>T (p.Arg1096Cys)	POLG (R1096C)	Single nucleotide variant (missense variant)	Mitochondrial disease	GLikely pathogenic FDA Recognized database
Select item 703069	NM_002693.3(POLG):c.3274-8C>T	POLG	Single nucleotide variant (intron variant)	Progressive sclerosing poliodystrophy +5 more	GLikely benign
Select item 1385866	NM_002693.3(POLG):c.3273+17G>A	POLG	Single nucleotide variant (intron variant)	Progressive sclerosing poliodystrophy +5 more	GConflicting classifications of pathogenicity
Select item 1315451	NM_002693.3(POLG):c.3227G>A (p.Gly1076Asp)	POLG (G1076D)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +6 more	GUncertain significance
Select item 206552	NM_002693.3(POLG):c.3215C>G (p.Thr1072Ser)	POLG (T1072S)	Single nucleotide variant (missense variant)	not provided +7 more	GUncertain significance
Select item 689441	NM_002693.3(POLG):c.3211C>T (p.Arg1071Cys)	POLG (R1071C)	Single nucleotide variant (missense variant)	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1 +6 more	GUncertain significance
Select item 388649	NM_002693.3(POLG):c.3204C>G (p.Asp1068Glu)	POLG (D1068E)	Single nucleotide variant (missense variant)	not provided +8 more	GUncertain significance
Select item 195487	NM_002693.3(POLG):c.3176A>G (p.Asn1059Ser)	POLG (N1059S)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +8 more	GUncertain significance
Select item 888159	NM_002693.3(POLG):c.3151G>T (p.Gly1051Trp)	POLG (G1051W)	Single nucleotide variant (missense variant)	POLG-Related Spectrum Disorders +7 more	GConflicting classifications of pathogenicity
Select item 129994	NM_002693.3(POLG):c.3131T>C (p.Val1044Ala)	POLG (V1044A)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia +11 more	GConflicting classifications of pathogenicity
Select item 422378	NM_002693.3(POLG):c.3104+2T>A	POLG	Single nucleotide variant (splice donor variant)	not provided +6 more	GLikely pathogenic
Select item 619308	NM_002693.3(POLG):c.3104+1G>A	POLG	Single nucleotide variant (splice donor variant)	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1 +6 more	GPathogenic/Likely pathogenic
Select item 206470	NM_002693.3(POLG):c.3098C>T (p.Ala1033Val)	POLG (A1033V)	Single nucleotide variant (missense variant)	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1 +7 more	GConflicting classifications of pathogenicity
Select item 206612	NM_002693.3(POLG):c.3077G>A (p.Arg1026His)	POLG (R1026H)	Single nucleotide variant (missense variant)	not provided +6 more	GUncertain significance
Select item 206546	NM_002693.3(POLG):c.3076C>T (p.Arg1026Cys)	POLG (R1026C)	Single nucleotide variant (missense variant)	not provided +8 more	GUncertain significance
Select item 405570	NM_002693.3(POLG):c.2977C>T (p.Arg993Cys)	POLG (R993C)	Single nucleotide variant (missense variant)	not specified +8 more	GUncertain significance
Select item 279961	NM_002693.3(POLG):c.2740A>C (p.Thr914Pro)	POLG (T914P)	Single nucleotide variant (missense variant)	Mitochondrial DNA depletion syndrome 4b +8 more	GPathogenic/Likely pathogenic
Select item 593514	NM_002693.3(POLG):c.2704C>G (p.Leu902Val)	POLG (L902V)	Single nucleotide variant (missense variant)	not provided +7 more	GUncertain significance
Select item 206528	NM_002693.3(POLG):c.2554C>T (p.Arg852Cys)	POLG (R852C)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia +9 more	GPathogenic
Select item 13502	NM_002693.3(POLG):c.2542G>A (p.Gly848Ser)	POLG (G848S)	Single nucleotide variant (missense variant)	Mitochondrial disease +12 more	GPathogenic
Select item 449762	NM_002693.3(POLG):c.2530G>A (p.Val844Met)	POLG (V844M)	Single nucleotide variant (missense variant)	not provided +6 more	GUncertain significance
Select item 218615	NM_002693.3(POLG):c.2510A>G (p.Tyr837Cys)	POLG (Y837C)	Single nucleotide variant (missense variant)	not specified +7 more	GUncertain significance
Select item 1405547	NM_002693.3(POLG):c.2485C>T (p.Pro829Ser)	POLG (P829S)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +5 more	GUncertain significance
Select item 448102	NM_002693.3(POLG):c.2468G>A (p.Arg823His)	POLG (R823H)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +7 more	GUncertain significance
Select item 194376	NM_002693.3(POLG):c.2369G>A (p.Arg790His)	POLG (R790H)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +9 more	GUncertain significance
Select item 1050879	NM_002693.3(POLG):c.2257C>T (p.Pro753Ser)	POLG (P753S)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +5 more	GUncertain significance
Select item 1017643	NM_002693.3(POLG):c.2255T>C (p.Leu752Pro)	POLG (L752P)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +6 more	GUncertain significance
Select item 206516	NM_002693.3(POLG):c.2207A>G (p.Asn736Ser)	POLG (N736S)	Single nucleotide variant (missense variant)	not provided +9 more	GConflicting classifications of pathogenicity
Select item 619398	NM_002693.3(POLG):c.2143C>T (p.Gln715Ter)	POLG (Q715*)	Single nucleotide variant (nonsense)	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis +5 more	GPathogenic
Select item 129990	NM_002693.3(POLG):c.2109C>A (p.Ala703=)	POLG	Single nucleotide variant (synonymous variant)	Progressive sclerosing poliodystrophy +9 more	GBenign/Likely benign
Select item 1396403	NM_002693.3(POLG):c.2094A>C (p.Glu698Asp)	POLG (E698D)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +5 more	GUncertain significance
Select item 206509	NM_002693.3(POLG):c.2085T>G (p.Asp695Glu)	POLG (D695E)	Single nucleotide variant (missense variant)	not specified +8 more	GUncertain significance
Select item 619415	NM_002693.3(POLG):c.2074GAA[1] (p.Glu693del)	POLG (E693del)	Microsatellite (inframe_deletion)	Progressive sclerosing poliodystrophy +5 more	GUncertain significance
Select item 579888	NM_002693.3(POLG):c.2069C>T (p.Thr690Met)	POLG (T690M)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +7 more	GUncertain significance
Select item 206508	NM_002693.3(POLG):c.2059A>G (p.Ile687Val)	POLG (I687V)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +7 more	GUncertain significance
Select item 451086	NM_002693.3(POLG):c.2027C>T (p.Ala676Val)	POLG (A676V)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +7 more	GConflicting classifications of pathogenicity
Select item 1036787	NM_002693.3(POLG):c.1936G>T (p.Val646Phe)	POLG (V646F)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +6 more	GUncertain significance
Select item 1361592	NM_002693.3(POLG):c.1907C>G (p.Thr636Arg)	POLG (T636R)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +5 more	GUncertain significance
Select item 458698	NM_002693.3(POLG):c.1882C>T (p.Arg628Trp)	POLG (R628W)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +5 more	GUncertain significance
Select item 571598	NM_002693.3(POLG):c.1669G>C (p.Glu557Gln)	POLG (E557Q)	Single nucleotide variant (missense variant)	not provided +6 more	GUncertain significance
Select item 432020	NM_002693.3(POLG):c.1613A>C (p.Glu538Ala)	POLG (E538A)	Single nucleotide variant (missense variant)	not provided +8 more	GUncertain significance
Select item 199081	NM_002693.3(POLG):c.1586-5del	MIR6766, POLG	Deletion (non-coding transcript variant +1 more)	Progressive sclerosing poliodystrophy +9 more	GBenign/Likely benign
Select item 206631	NM_002693.3(POLG):c.1570C>G (p.Pro524Ala)	POLG (P524A)	Single nucleotide variant (missense variant)	not provided +6 more	GUncertain significance
Select item 13510	NM_002693.3(POLG):c.1491G>C (p.Gln497His)	POLG (Q497H)	Single nucleotide variant (missense variant)	not provided +7 more	GUncertain significance
Select item 1444207	NM_002693.3(POLG):c.1433+5C>T	POLG	Single nucleotide variant (intron variant)	Progressive sclerosing poliodystrophy +5 more	GUncertain significance
Select item 280017	NM_002693.3(POLG):c.1433+1G>A	POLG	Single nucleotide variant (splice donor variant)	not provided +6 more	GPathogenic
Select item 502761	NM_002693.3(POLG):c.1420C>A (p.Leu474Ile)	POLG (L474I)	Single nucleotide variant (missense variant)	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis +6 more	GUncertain significance
Select item 206630	NM_002693.3(POLG):c.1403A>G (p.Asn468Ser)	POLG (N468S)	Single nucleotide variant (missense variant)	not specified +8 more	GUncertain significance
Select item 206596	NM_002693.3(POLG):c.1402A>G (p.Asn468Asp)	POLG (N468D)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia +13 more	GConflicting classifications of pathogenicity
Select item 13496	NM_002693.3(POLG):c.1399G>A (p.Ala467Thr)	POLG (A467T)	Single nucleotide variant (missense variant)	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1 +12 more	GPathogenic
Select item 206593	NM_002693.3(POLG):c.1328G>A (p.Arg443His)	POLG (R443H)	Single nucleotide variant (missense variant)	not provided +6 more	GUncertain significance
Select item 458687	NM_002693.3(POLG):c.1276G>A (p.Gly426Ser)	POLG (G426S)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +6 more	GConflicting classifications of pathogenicity
Select item 198151	NM_002693.3(POLG):c.1174C>G (p.Leu392Val)	POLG (L392V)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +10 more	GConflicting classifications of pathogenicity
Select item 138773	NM_002693.3(POLG):c.1126C>T (p.Leu376=)	POLG	Single nucleotide variant (synonymous variant)	not provided +8 more	GBenign/Likely benign
Select item 291293	NM_002693.3(POLG):c.1097G>C (p.Gly366Ala)	POLG (G366A)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +6 more	GUncertain significance
Select item 1564682	NM_002693.3(POLG):c.1023+17G>A	POLG	Single nucleotide variant (intron variant)	Progressive sclerosing poliodystrophy +5 more	GLikely benign
Select item 1354124	NM_002693.3(POLG):c.995C>T (p.Ser332Phe)	POLG (S332F)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +5 more	GUncertain significance
Select item 280375	NM_002693.3(POLG):c.925C>T (p.Arg309Cys)	POLG (R309C)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +6 more	GPathogenic
Select item 13497	NM_002693.3(POLG):c.911T>G (p.Leu304Arg)	POLG (L304R)	Single nucleotide variant (missense variant)	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1 +9 more	GPathogenic/Likely pathogenic
Select item 648222	NM_002693.3(POLG):c.869G>A (p.Arg290His)	POLG (R290H)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +6 more	GUncertain significance
Select item 1063541	NM_002693.3(POLG):c.856-3C>T	POLG	Single nucleotide variant (intron variant)	not specified +6 more	GUncertain significance
Select item 619447	NM_002693.3(POLG):c.824G>A (p.Arg275Gln)	POLG (R275Q)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +5 more	GConflicting classifications of pathogenicity
Select item 593213	NM_002693.3(POLG):c.739C>G (p.Leu247Val)	POLG (L247V)	Single nucleotide variant (missense variant)	not provided +7 more	GUncertain significance
Select item 861889	NM_002693.3(POLG):c.730C>G (p.Leu244Val)	POLG (L244V)	Single nucleotide variant (missense variant)	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1 +5 more	GConflicting classifications of pathogenicity
Select item 452496	NM_002693.3(POLG):c.729C>A (p.Asp243Glu)	POLG (D243E)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +7 more	GUncertain significance
Select item 206582	NM_002693.3(POLG):c.719C>T (p.Ser240Leu)	POLG, POLGARF (S240L)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +6 more	GUncertain significance
Select item 432673	NM_002693.3(POLG):c.629C>T (p.Thr210Ile)	POLG, POLGARF (T210I)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +6 more	GUncertain significance
Select item 21318	NM_002693.3(POLG):c.578G>A (p.Arg193Gln)	POLG, POLGARF (R193Q)	Single nucleotide variant (missense variant)	Mitochondrial disease	GUncertain significance FDA Recognized database
Select item 587834	NM_002693.3(POLG):c.431A>G (p.Gln144Arg)	POLG, POLGARF (Q144R)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +8 more	GUncertain significance
Select item 966409	NM_002693.3(POLG):c.402C>G (p.Asn134Lys)	POLG, POLGARF (N134K)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +6 more	GUncertain significance
Select item 206620	NM_002693.3(POLG):c.346C>T (p.Pro116Ser)	POLG, POLGARF (P116S)	Single nucleotide variant (missense variant)	not provided +6 more	GConflicting classifications of pathogenicity
Select item 807308	NM_002693.3(POLG):c.331G>C (p.Gly111Arg)	POLG, POLGARF (G111R)	Single nucleotide variant (missense variant)	not provided +6 more	GUncertain significance
Select item 1061081	NM_002693.3(POLG):c.200G>C (p.Gly67Ala)	POLG, POLGARF (G67A)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +5 more	GUncertain significance
Select item 206482	NM_002693.3(POLG):c.126GCA[14] (p.Gln53_Gln55dup)	POLG, POLGARF	Microsatellite (inframe_insertion)	Inborn genetic diseases +8 more	GBenign/Likely benign
Select item 167522	NM_002693.3(POLG):c.126GCA[12] (p.Gln55dup)	POLG, POLGARF	Microsatellite (inframe_insertion)	not provided +11 more	GBenign/Likely benign
Select item 206481	NM_002693.3(POLG):c.126GCA[8] (p.Gln53_Gln55del)	POLG, POLGARF	Microsatellite (inframe_deletion)	Mitochondrial DNA depletion syndrome 4b +9 more	GBenign/Likely benign
Select item 206478	NM_002693.3(POLG):c.126GCA[5] (p.Gln50_Gln55del)	POLG, POLGARF	Microsatellite (inframe_deletion)	Inborn genetic diseases +8 more	GConflicting classifications of pathogenicity
Select item 167523	NM_002693.3(POLG):c.126GCA[9] (p.Gln54_Gln55del)	POLG, POLGARF	Microsatellite (inframe_deletion)	not specified +8 more	GBenign/Likely benign
Select item 195176	NM_002693.3(POLG):c.114G>T (p.Gly38=)	POLG, POLGARF	Single nucleotide variant (synonymous variant)	Progressive sclerosing poliodystrophy +6 more	GConflicting classifications of pathogenicity
Select item 206550	NM_002693.3(POLG):c.86C>G (p.Ser29Cys)	POLGARF, POLG (S29C)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +6 more	GUncertain significance
Select item 195182	NM_002693.3(POLG):c.32G>A (p.Gly11Asp)	POLG, POLGARF (G11D)	Single nucleotide variant (missense variant)	Progressive sclerosing poliodystrophy +11 more	GConflicting classifications of pathogenicity
Select item 413484	NM_002693.3(POLG):c.30C>T (p.Ala10=)	POLG, POLGARF	Single nucleotide variant (synonymous variant)	Progressive sclerosing poliodystrophy +5 more	GLikely benign
Select item 223048	NM_001953.5(TYMP):c.931G>A (p.Gly311Ser)	LOC130067862, TYMP (G311S)	Single nucleotide variant (missense variant)	Mitochondrial DNA depletion syndrome 1 +1 more	GUncertain significance
Select item 16653	NM_001953.5(TYMP):c.866A>C (p.Glu289Ala)	TYMP (E289A)	Single nucleotide variant (missense variant)	Mitochondrial DNA depletion syndrome 1 +1 more	GPathogenic
Select item 1310683	NM_001953.5(TYMP):c.862G>A (p.Glu288Lys)	TYMP (E288K)	Single nucleotide variant (missense variant)	Mitochondrial DNA depletion syndrome 1 +1 more	GUncertain significance
Select item 342144	NM_001953.5(TYMP):c.859G>A (p.Val287Met)	TYMP (V287M)	Single nucleotide variant (missense variant)	Mitochondrial DNA depletion syndrome 1 +1 more	GUncertain significance
Select item 1400246	NM_001953.5(TYMP):c.736G>A (p.Glu246Lys)	TYMP (E246K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 16663	NM_001953.5(TYMP):c.622G>A (p.Val208Met)	TYMP (V208M)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 16660	NM_001953.5(TYMP):c.457G>A (p.Gly153Ser)	TYMP (G153S)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic

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