ClinVar Miner

List of variants in gene POLG reported as benign for not provided

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Total variants: 28
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HGVS dbSNP
NM_002693.2(POLG):c.1250+188A>G
NM_002693.2(POLG):c.1251-43C>T rs2307444
NM_002693.2(POLG):c.1251-88dup
NM_002693.2(POLG):c.126_128GCA[10] (p.Gln55del) rs41550117
NM_002693.2(POLG):c.126_128GCA[12] (p.Gln55dup) rs41550117
NM_002693.2(POLG):c.126_128GCA[13] (p.Gln54_Gln55dup) rs41550117
NM_002693.2(POLG):c.1550G>T (p.Gly517Val) rs61752783
NM_002693.2(POLG):c.1712+110T>C
NM_002693.2(POLG):c.1712+177C>T
NM_002693.2(POLG):c.1712+238C>T
NM_002693.2(POLG):c.1984G>A (p.Glu662Lys) rs2307450
NM_002693.2(POLG):c.2254C>T (p.Leu752=) rs41564016
NM_002693.2(POLG):c.2265+236G>A
NM_002693.2(POLG):c.2266-153C>T
NM_002693.2(POLG):c.2266-227A>G
NM_002693.2(POLG):c.2426+281A>G
NM_002693.2(POLG):c.2427-240C>T
NM_002693.2(POLG):c.2981+206C>A
NM_002693.2(POLG):c.2981+283A>C
NM_002693.2(POLG):c.2982-331G>T
NM_002693.2(POLG):c.2982-332T>G
NM_002693.2(POLG):c.2994G>C (p.Ser998=) rs567030498
NM_002693.2(POLG):c.3198G>A (p.Thr1066=) rs61752780
NM_002693.2(POLG):c.3483-164A>C
NM_002693.2(POLG):c.3559C>T (p.Arg1187Trp) rs369544574
NM_002693.2(POLG):c.3597C>A (p.Thr1199=) rs2307443
NM_002693.2(POLG):c.659+284G>C
NM_002693.2(POLG):c.660-290T>C

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