ClinVar Miner

Variants in gene POLR3A with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 19
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HGVS dbSNP gnomAD frequency
NM_007055.4(POLR3A):c.1724A>T (p.Lys575Met) rs56214655 0.01630
NM_007055.4(POLR3A):c.2247+27C>T rs143228905 0.01170
NM_007055.4(POLR3A):c.885+19C>G rs12263414 0.01064
NM_007055.4(POLR3A):c.1566G>T (p.Leu522=) rs12255950 0.01052
NM_007055.4(POLR3A):c.3645C>T (p.Asp1215=) rs147591223 0.00606
NM_007055.4(POLR3A):c.2938A>G (p.Ile980Val) rs146253630 0.00599
NM_007055.4(POLR3A):c.3987T>C (p.Phe1329=) rs16935497 0.00487
NM_007055.4(POLR3A):c.741G>A (p.Pro247=) rs12764690 0.00484
NM_007055.4(POLR3A):c.3846C>T (p.Ile1282=) rs116197727 0.00444
NM_007055.4(POLR3A):c.3660G>A (p.Lys1220=) rs141312907 0.00313
NM_007055.4(POLR3A):c.927C>T (p.Asp309=) rs41274610 0.00287
NM_007055.4(POLR3A):c.2472C>T (p.His824=) rs139259717 0.00220
NM_007055.4(POLR3A):c.2334C>T (p.Leu778=) rs144671070 0.00187
NM_007055.4(POLR3A):c.2604G>A (p.Thr868=) rs142834115 0.00155
NM_007055.4(POLR3A):c.4071C>T (p.Thr1357=) rs140044475 0.00120
NM_007055.4(POLR3A):c.1745G>A (p.Arg582His) rs34588967
NM_007055.4(POLR3A):c.1745G>T (p.Arg582Leu) rs34588967
NM_007055.4(POLR3A):c.1771-6C>T rs115020338
NM_007055.4(POLR3A):c.1771-7C>T rs201314157

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