List of variants in gene THPO reported as uncertain significance for hematologic disorder

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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: 29

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HGVS	dbSNP	gnomAD frequency
NM_000460.4(THPO):c.-56G>A	rs187556243	0.00053
NM_000460.4(THPO):c.*366G>C	rs542821225	0.00047
NM_000460.4(THPO):c.*404G>A	rs573846929	0.00013
NM_000460.4(THPO):c.579C>T (p.Asn193=)	rs202166253	0.00010
NM_000460.4(THPO):c.889A>G (p.Thr297Ala)	rs530613857	0.00010
NM_000460.4(THPO):c.*27A>G	rs201864435	0.00009
NM_000460.4(THPO):c.*480G>A	rs778078910	0.00006
NM_000460.4(THPO):c.-215T>A	rs886058219	0.00004
NM_000460.4(THPO):c.963C>T (p.His321=)	rs377138170	0.00004
NM_000460.4(THPO):c.183G>T (p.Leu61=)	rs200666378	0.00003
NM_000460.4(THPO):c.14-11C>T	rs745850672	0.00001
NM_000460.4(THPO):c.303A>G (p.Gln101=)	rs775232517	0.00001
NM_000460.4(THPO):c.518T>C (p.Val173Ala)	rs768776540	0.00001
NM_000460.4(THPO):c.796C>T (p.Arg266Cys)	rs186070598	0.00001
NM_000460.4(THPO):c.808G>A (p.Gly270Arg)	rs759569299	0.00001
NM_001290003.1(THPO):c.98C>T (p.Pro33Leu)	rs1208732776	0.00001
NM_000460.4(THPO):c.*108C>T	rs1353316698
NM_000460.4(THPO):c.*191T>G	rs1713957283
NM_000460.4(THPO):c.*500A>G	rs886058217
NM_000460.4(THPO):c.-123C>T	rs535707667
NM_000460.4(THPO):c.114del (p.Asp39fs)	rs768078445
NM_000460.4(THPO):c.13G>A (p.Glu5Lys)	rs1460650949
NM_000460.4(THPO):c.233A>G (p.Glu78Gly)	rs1447030119
NM_000460.4(THPO):c.482G>A (p.Arg161His)
NM_000460.4(THPO):c.517G>A (p.Val173Ile)	rs780992873
NM_000460.4(THPO):c.610dup (p.Glu204fs)	rs776536238
NM_000460.4(THPO):c.671G>A (p.Gly224Glu)	rs886058218
NM_000460.4(THPO):c.740T>C (p.Leu247Pro)	rs749011920
NM_000460.4(THPO):c.791_794del (p.Pro264fs)	rs760659440

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