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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 37

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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	0.00004
NM_001063.4(TF):c.686T>C (p.Ile229Thr)	rs764361166	0.00004
NM_001063.4(TF):c.790C>G (p.Gln264Glu)	rs766883577	0.00004
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.113G>A (p.Cys38Tyr)
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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