ClinVar Miner

List of variants reported as likely pathogenic for Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type by Baylor Genetics

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Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_133259.4(LRPPRC):c.515A>G (p.Tyr172Cys) rs187584458 0.00003
NM_133259.4(LRPPRC):c.1723C>T (p.Arg575Ter) rs774934005 0.00001
NM_133259.4(LRPPRC):c.2326G>T (p.Glu776Ter) rs758615834 0.00001
NM_133259.4(LRPPRC):c.244C>T (p.Gln82Ter) rs754855090 0.00001
NM_133259.4(LRPPRC):c.650+1G>C rs1249427615 0.00001
NM_133259.4(LRPPRC):c.1091C>G (p.Ser364Ter) rs1553410995
NM_133259.4(LRPPRC):c.1092_1095del (p.Glu366fs) rs2103713116
NM_133259.4(LRPPRC):c.1156-2A>C
NM_133259.4(LRPPRC):c.1165_1198del (p.Lys389fs)
NM_133259.4(LRPPRC):c.1216_1237dup (p.Cys413fs)
NM_133259.4(LRPPRC):c.1389_1393del (p.Lys463fs)
NM_133259.4(LRPPRC):c.1544_1548dup (p.Ala517fs)
NM_133259.4(LRPPRC):c.1589C>A (p.Ser530Ter) rs775735922
NM_133259.4(LRPPRC):c.1612C>T (p.Gln538Ter) rs1553406772
NM_133259.4(LRPPRC):c.1677+1G>T rs2103624540
NM_133259.4(LRPPRC):c.1695C>G (p.Tyr565Ter) rs1672822541
NM_133259.4(LRPPRC):c.1722_1723del (p.Gly576fs) rs750343121
NM_133259.4(LRPPRC):c.1735+2T>C
NM_133259.4(LRPPRC):c.1775del (p.Met592fs)
NM_133259.4(LRPPRC):c.1865_1868del (p.Ile622fs) rs752914914
NM_133259.4(LRPPRC):c.1944_1947del (p.Ser648fs)
NM_133259.4(LRPPRC):c.1965+2T>C
NM_133259.4(LRPPRC):c.1966-2A>G
NM_133259.4(LRPPRC):c.1972C>T (p.Gln658Ter)
NM_133259.4(LRPPRC):c.2024dup (p.Asn675fs)
NM_133259.4(LRPPRC):c.205C>T (p.Gln69Ter)
NM_133259.4(LRPPRC):c.2086C>T (p.Gln696Ter)
NM_133259.4(LRPPRC):c.2167C>T (p.Arg723Ter) rs1022152551
NM_133259.4(LRPPRC):c.2211-1G>A
NM_133259.4(LRPPRC):c.2225C>A (p.Ser742Ter)
NM_133259.4(LRPPRC):c.2285del (p.Gly762fs)
NM_133259.4(LRPPRC):c.2369dup (p.His791fs) rs2105077651
NM_133259.4(LRPPRC):c.245del (p.Gln82fs)
NM_133259.4(LRPPRC):c.251_254del (p.Asp84fs) rs1553413047
NM_133259.4(LRPPRC):c.2545_2558del (p.Tyr849fs) rs1553400685
NM_133259.4(LRPPRC):c.2559dup (p.Val854fs)
NM_133259.4(LRPPRC):c.2569_2585del (p.Arg857fs)
NM_133259.4(LRPPRC):c.2630-5_2630-2del
NM_133259.4(LRPPRC):c.283C>T (p.Arg95Ter) rs760186575
NM_133259.4(LRPPRC):c.2986_3001del (p.Leu996fs)
NM_133259.4(LRPPRC):c.3003_3006del (p.Glu1002fs) rs1300725076
NM_133259.4(LRPPRC):c.3031del (p.Val1011fs)
NM_133259.4(LRPPRC):c.3044G>A (p.Trp1015Ter)
NM_133259.4(LRPPRC):c.3148+1G>T
NM_133259.4(LRPPRC):c.3149-2A>T
NM_133259.4(LRPPRC):c.3151del
NM_133259.4(LRPPRC):c.320_321del (p.Lys107fs)
NM_133259.4(LRPPRC):c.3254_3255del (p.Gln1085fs)
NM_133259.4(LRPPRC):c.346+1G>T
NM_133259.4(LRPPRC):c.3563_3566del (p.Ile1188fs)
NM_133259.4(LRPPRC):c.3566dup (p.Asn1190fs) rs762254417
NM_133259.4(LRPPRC):c.3645C>G (p.Tyr1215Ter)
NM_133259.4(LRPPRC):c.3737_3740del (p.Asn1246fs)
NM_133259.4(LRPPRC):c.3773dup (p.Leu1259fs) rs761052211
NM_133259.4(LRPPRC):c.3826-1G>A
NM_133259.4(LRPPRC):c.3928_3938del (p.Leu1310fs)
NM_133259.4(LRPPRC):c.3941T>G (p.Leu1314Ter)
NM_133259.4(LRPPRC):c.3979_3981delinsGG (p.Ser1327fs)
NM_133259.4(LRPPRC):c.3979del (p.Ser1327fs)
NM_133259.4(LRPPRC):c.3985+1811_4077delinsA
NM_133259.4(LRPPRC):c.4114_4115insAT (p.Phe1372fs)
NM_133259.4(LRPPRC):c.451del (p.Asp151fs)
NM_133259.4(LRPPRC):c.456_457del (p.Leu153fs)
NM_133259.4(LRPPRC):c.495T>G (p.Tyr165Ter)
NM_133259.4(LRPPRC):c.580del (p.Gln194fs)
NM_133259.4(LRPPRC):c.589C>T (p.Arg197Ter) rs989113962
NM_133259.4(LRPPRC):c.650+1G>A
NM_133259.4(LRPPRC):c.650+1del
NM_133259.4(LRPPRC):c.738-1G>A
NM_133259.4(LRPPRC):c.738-2A>C

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