ClinVar Miner

List of variants in gene TF reported as uncertain significance for anemia

Included ClinVar conditions (280):
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Gene type:
ClinVar version:
Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_001063.4(TF):c.829G>A (p.Gly277Ser) rs1799899 0.04529
NM_001063.4(TF):c.1027C>T (p.Arg343Trp) rs150854910 0.00096
NM_001063.4(TF):c.228G>A (p.Ala76=) rs140381335 0.00072
NM_001063.4(TF):c.43+8C>A rs368521553 0.00043
NM_001063.4(TF):c.1107C>T (p.His369=) rs112157819 0.00030
NM_001063.4(TF):c.119G>A (p.Ser40Asn) rs146477698 0.00030
NM_001063.4(TF):c.281A>G (p.Asn94Ser) rs200551981 0.00020
NM_001063.4(TF):c.1095G>A (p.Ala365=) rs575999145 0.00016
NM_001063.4(TF):c.165T>A (p.Ser55Arg) rs8177318 0.00016
NM_001063.4(TF):c.1352T>C (p.Val451Ala) rs142116896 0.00014
NM_001063.4(TF):c.215C>T (p.Ala72Val) rs142819812 0.00011
NM_001063.4(TF):c.1044C>T (p.Gly348=) rs139468631 0.00010
NM_001063.3(TF):c.-117G>A rs540606355 0.00009
NM_001063.4(TF):c.585G>A (p.Gly195=) rs376851470 0.00009
NM_001063.4(TF):c.*361T>C rs952581393 0.00008
NM_001063.4(TF):c.-18C>T rs781336514 0.00008
NM_001063.4(TF):c.1615G>A (p.Ala539Thr) rs369813809 0.00007
NM_001063.4(TF):c.154G>A (p.Asp52Asn) rs41298295 0.00006
NM_001063.4(TF):c.334A>G (p.Thr112Ala) rs199624323 0.00006
NM_001063.4(TF):c.790C>G (p.Gln264Glu) rs766883577 0.00004
NM_001063.4(TF):c.686T>C (p.Ile229Thr) rs764361166 0.00003
NM_001063.4(TF):c.502+12G>A rs201033555 0.00002
NM_001063.4(TF):c.828C>T (p.Gly276=) rs769998552 0.00002
NM_001063.4(TF):c.1029G>A (p.Arg343=) rs762383370 0.00001
NM_001063.4(TF):c.1198A>G (p.Ile400Val) rs200250866 0.00001
NM_001063.4(TF):c.1204-14C>A rs1406126776 0.00001
NM_001063.4(TF):c.1785C>T (p.Asn595=) rs757985238 0.00001
NM_001063.4(TF):c.311A>G (p.Tyr104Cys) rs746672239 0.00001
NM_001063.4(TF):c.60C>T (p.Val20=) rs756125441 0.00001
NM_001063.4(TF):c.680C>T (p.Ser227Leu) rs1295939213 0.00001
NM_001063.4(TF):c.*81A>G rs886058015
NM_001063.4(TF):c.142G>A (p.Val48Ile) rs144636315
NM_001063.4(TF):c.1687+9A>C rs886058014
NM_001063.4(TF):c.174T>A (p.Cys58Ter) rs1559867036
NM_001063.4(TF):c.1805C>A (p.Pro602Gln) rs41296598
NM_001063.4(TF):c.2063-11_2063-10del rs2107937266

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