List of variants in gene F13B reported as uncertain significance for hematologic disorder

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: 48

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HGVS	dbSNP	gnomAD frequency
NM_001994.3(F13B):c.1049A>G (p.His350Arg)	rs5999	0.00858
NM_001994.3(F13B):c.765C>T (p.Cys255=)	rs5994	0.00807
NM_001994.3(F13B):c.570G>A (p.Lys190=)	rs17514253	0.00792
NM_001994.3(F13B):c.1586T>C (p.Leu529Pro)	rs17549671	0.00764
NM_001994.3(F13B):c.1025T>C (p.Ile342Thr)	rs17514281	0.00637
NM_001994.3(F13B):c.1902G>A (p.Met634Ile)	rs142886126	0.00281
NM_001994.3(F13B):c.1163A>T (p.Glu388Val)	rs5991	0.00175
NM_001994.3(F13B):c.*162C>A	rs180977741	0.00131
NM_001994.3(F13B):c.1935A>T (p.Arg645Ser)	rs149091258	0.00104
NM_001994.3(F13B):c.1089A>C (p.Ala363=)	rs117019969	0.00047
NM_001994.3(F13B):c.986-4T>C	rs76405247	0.00046
NM_001994.3(F13B):c.1228G>A (p.Gly410Arg)	rs144134146	0.00042
NM_001994.3(F13B):c.1285T>C (p.Tyr429His)	rs201427054	0.00029
NM_001994.3(F13B):c.354C>T (p.Cys118=)	rs142562955	0.00026
NM_001994.3(F13B):c.1257C>A (p.Ser419=)	rs761403510	0.00021
NM_001994.3(F13B):c.1320A>G (p.Glu440=)	rs147383994	0.00009
NM_001994.3(F13B):c.1670A>G (p.His557Arg)	rs759631235	0.00006
NM_001994.3(F13B):c.1815C>T (p.His605=)	rs375961962	0.00006
NM_001994.3(F13B):c.796G>C (p.Val266Leu)	rs533222920	0.00005
NM_001994.3(F13B):c.1060T>C (p.Tyr354His)	rs376295989	0.00004
NM_001994.3(F13B):c.-30T>A	rs767006990	0.00003
NM_001994.3(F13B):c.224C>T (p.Thr75Met)	rs915458369	0.00003
NM_001994.3(F13B):c.1098C>T (p.Ser366=)	rs771474972	0.00002
NM_001994.3(F13B):c.1942C>T (p.Pro648Ser)	rs759996311	0.00002
NM_001994.3(F13B):c.877C>T (p.Arg293Cys)	rs780257236	0.00002
NM_001994.3(F13B):c.-23C>A	rs761442589	0.00001
NM_001994.3(F13B):c.1145A>G (p.Lys382Arg)	rs755966271	0.00001
NM_001994.3(F13B):c.1877A>G (p.Tyr626Cys)	rs201438197	0.00001
NM_001994.3(F13B):c.645_647del (p.Leu216del)	rs750927097	0.00001
NM_001994.3(F13B):c.675T>A (p.His225Gln)	rs182353865	0.00001
NM_001994.3(F13B):c.1079T>A (p.Val360Glu)	rs2125068039
NM_001994.3(F13B):c.1106T>C (p.Leu369Pro)	rs1655669695
NM_001994.3(F13B):c.1317C>T (p.Cys439=)	rs149466650
NM_001994.3(F13B):c.1520GAG[1] (p.Gly508del)
NM_001994.3(F13B):c.1556-13C>A	rs149088047
NM_001994.3(F13B):c.1693G>A (p.Ala565Thr)	rs2125062488
NM_001994.3(F13B):c.1739-8_1739-6del	rs556380704
NM_001994.3(F13B):c.1961C>T (p.Ser654Phe)	rs561359007
NM_001994.3(F13B):c.431C>T (p.Pro144Leu)	rs1558311941
NM_001994.3(F13B):c.521A>T (p.Asp174Val)	rs2125072085
NM_001994.3(F13B):c.625A>G (p.Thr209Ala)	rs201594137
NM_001994.3(F13B):c.779G>T (p.Trp260Leu)	rs2125071222
NM_001994.3(F13B):c.815A>G (p.Asn272Ser)	rs1655688114
NM_001994.3(F13B):c.86A>T (p.His29Leu)
NM_001994.3(F13B):c.874T>G (p.Tyr292Asp)	rs1247793701
NM_001994.3(F13B):c.881A>T (p.His294Leu)	rs2125068412
NM_001994.3(F13B):c.889A>C (p.Ile297Leu)	rs1655684285
NM_001994.3(F13B):c.96T>C (p.Asn32=)	rs1655924673

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