ClinVar Miner

List of variants in gene F13B studied for coagulation protein disease

Included ClinVar conditions (43):
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Gene type:
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Total variants: 33
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HGVS dbSNP
F13B, 1-BP DEL, IVS1AS, A, -2
F13B, 3-BP INS, AAC
NM_001994.2(F13B):c.*143G>A rs698859
NM_001994.2(F13B):c.*162C>A rs180977741
NM_001994.2(F13B):c.*89G>C rs17549873
NM_001994.2(F13B):c.-30T>A rs767006990
NM_001994.2(F13B):c.1025T>C (p.Ile342Thr) rs17514281
NM_001994.2(F13B):c.1060T>C (p.Tyr354His) rs376295989
NM_001994.2(F13B):c.1089A>C (p.Ala363=) rs117019969
NM_001994.2(F13B):c.1098C>T (p.Ser366=) rs771474972
NM_001994.2(F13B):c.1145A>G (p.Lys382Arg) rs755966271
NM_001994.2(F13B):c.1163A>T (p.Glu388Val) rs5991
NM_001994.2(F13B):c.1285T>C (p.Tyr429His) rs201427054
NM_001994.2(F13B):c.1320A>G (p.Glu440=) rs147383994
NM_001994.2(F13B):c.1349G>T (p.Cys450Phe) rs121913075
NM_001994.2(F13B):c.1498del (p.Glu500fs) rs797044453
NM_001994.2(F13B):c.1556-13C>A rs149088047
NM_001994.2(F13B):c.1670A>G (p.His557Arg) rs759631235
NM_001994.2(F13B):c.1707T>G (p.Asp569Glu) rs6000
NM_001994.2(F13B):c.1739-8_1739-6del rs556380704
NM_001994.2(F13B):c.1806T>C (p.Asn602=) rs5998
NM_001994.2(F13B):c.1815C>T (p.His605=) rs375961962
NM_001994.2(F13B):c.1902G>A (p.Met634Ile) rs142886126
NM_001994.2(F13B):c.1961C>T (p.Ser654Phe) rs561359007
NM_001994.2(F13B):c.299_300insAAC (p.Tyr100Ter)
NM_001994.2(F13B):c.344G>A (p.Arg115His) rs6003
NM_001994.2(F13B):c.354C>T (p.Cys118=) rs142562955
NM_001994.2(F13B):c.456A>G (p.Thr152=) rs5997
NM_001994.2(F13B):c.570G>A (p.Lys190=) rs17514253
NM_001994.2(F13B):c.645_647del (p.Leu216del) rs750927097
NM_001994.2(F13B):c.796G>C (p.Val266Leu) rs533222920
NM_001994.2(F13B):c.877C>T (p.Arg293Cys) rs780257236
NM_001994.2(F13B):c.986-4T>C rs76405247

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