ClinVar Miner

List of variants in gene POLR3F reported as uncertain significance for not provided

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Total variants: 83
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HGVS dbSNP gnomAD frequency
NC_000020.10:g.(?_18455699)_(18455851_?)dup
NM_006466.4(POLR3F):c.133A>G (p.Ile45Val)
NM_006466.4(POLR3F):c.134T>C (p.Ile45Thr)
NM_006466.4(POLR3F):c.160A>G (p.Ile54Val)
NM_006466.4(POLR3F):c.180+4A>G
NM_006466.4(POLR3F):c.185A>G (p.Gln62Arg)
NM_006466.4(POLR3F):c.206A>G (p.Asn69Ser)
NM_006466.4(POLR3F):c.208A>T (p.Thr70Ser)
NM_006466.4(POLR3F):c.209C>T (p.Thr70Met)
NM_006466.4(POLR3F):c.227T>A (p.Ile76Lys)
NM_006466.4(POLR3F):c.230A>G (p.Lys77Arg)
NM_006466.4(POLR3F):c.234C>T (p.Asp78=)
NM_006466.4(POLR3F):c.248G>A (p.Gly83Asp)
NM_006466.4(POLR3F):c.249-12A>G
NM_006466.4(POLR3F):c.249-4A>G
NM_006466.4(POLR3F):c.301G>A (p.Asp101Asn)
NM_006466.4(POLR3F):c.308G>A (p.Gly103Glu)
NM_006466.4(POLR3F):c.311A>G (p.Asn104Ser)
NM_006466.4(POLR3F):c.316+15G>C
NM_006466.4(POLR3F):c.316+3A>G
NM_006466.4(POLR3F):c.316+7del
NM_006466.4(POLR3F):c.317-3T>C
NM_006466.4(POLR3F):c.317G>A (p.Gly106Glu)
NM_006466.4(POLR3F):c.322T>G (p.Trp108Gly)
NM_006466.4(POLR3F):c.341A>G (p.Tyr114Cys)
NM_006466.4(POLR3F):c.344A>G (p.Lys115Arg)
NM_006466.4(POLR3F):c.355C>T (p.Pro119Ser)
NM_006466.4(POLR3F):c.407_409del (p.Ile136del)
NM_006466.4(POLR3F):c.429+17T>C
NM_006466.4(POLR3F):c.429+4A>G
NM_006466.4(POLR3F):c.430-10T>C
NM_006466.4(POLR3F):c.438A>G (p.Lys146=)
NM_006466.4(POLR3F):c.440del (p.Lys147fs)
NM_006466.4(POLR3F):c.443dup (p.Val149fs)
NM_006466.4(POLR3F):c.444G>A (p.Lys148=)
NM_006466.4(POLR3F):c.456C>G (p.Leu152=)
NM_006466.4(POLR3F):c.476G>A (p.Arg159Gln)
NM_006466.4(POLR3F):c.478T>C (p.Ser160Pro)
NM_006466.4(POLR3F):c.498dup (p.Tyr167fs)
NM_006466.4(POLR3F):c.526T>C (p.Phe176Leu)
NM_006466.4(POLR3F):c.534G>A (p.Glu178=)
NM_006466.4(POLR3F):c.569C>A (p.Ser190Tyr)
NM_006466.4(POLR3F):c.574-10A>G
NM_006466.4(POLR3F):c.574-16G>A
NM_006466.4(POLR3F):c.580A>G (p.Thr194Ala)
NM_006466.4(POLR3F):c.586C>T (p.Arg196Ter)
NM_006466.4(POLR3F):c.587G>A (p.Arg196Gln)
NM_006466.4(POLR3F):c.593G>C (p.Ser198Thr)
NM_006466.4(POLR3F):c.593G>T (p.Ser198Ile)
NM_006466.4(POLR3F):c.603C>T (p.Asn201=)
NM_006466.4(POLR3F):c.607A>G (p.Met203Val)
NM_006466.4(POLR3F):c.617G>A (p.Arg206Lys)
NM_006466.4(POLR3F):c.622A>G (p.Ser208Gly)
NM_006466.4(POLR3F):c.648G>A (p.Val216=)
NM_006466.4(POLR3F):c.663C>T (p.Cys221=)
NM_006466.4(POLR3F):c.664G>A (p.Glu222Lys)
NM_006466.4(POLR3F):c.676A>C (p.Ser226Arg)
NM_006466.4(POLR3F):c.681+2T>C
NM_006466.4(POLR3F):c.681+8C>G
NM_006466.4(POLR3F):c.682-5T>G
NM_006466.4(POLR3F):c.695T>A (p.Met232Lys)
NM_006466.4(POLR3F):c.722C>T (p.Thr241Ile)
NM_006466.4(POLR3F):c.752C>T (p.Thr251Met)
NM_006466.4(POLR3F):c.821A>G (p.Asn274Ser)
NM_006466.4(POLR3F):c.839_840inv (p.Thr280Met)
NM_006466.4(POLR3F):c.850C>A (p.Arg284=)
NM_006466.4(POLR3F):c.850C>T (p.Arg284Trp)
NM_006466.4(POLR3F):c.851G>A (p.Arg284Gln)
NM_006466.4(POLR3F):c.859_860insAGGGCACCCT (p.Cys287Ter)
NM_006466.4(POLR3F):c.870C>T (p.Cys290=)
NM_006466.4(POLR3F):c.872C>T (p.Pro291Leu)
NM_006466.4(POLR3F):c.873+10A>G
NM_006466.4(POLR3F):c.873+4A>G
NM_006466.4(POLR3F):c.873G>A (p.Pro291=)
NM_006466.4(POLR3F):c.874-15_874-12del
NM_006466.4(POLR3F):c.884A>T (p.Asp295Val)
NM_006466.4(POLR3F):c.885C>A (p.Asp295Glu)
NM_006466.4(POLR3F):c.892G>A (p.Glu298Lys)
NM_006466.4(POLR3F):c.907del (p.Ser303fs)
NM_006466.4(POLR3F):c.916A>G (p.Asn306Asp)
NM_006466.4(POLR3F):c.918C>A (p.Asn306Lys)
NM_006466.4(POLR3F):c.920G>T (p.Cys307Phe)
NM_006466.4(POLR3F):c.943G>A (p.Glu315Lys)

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