ClinVar Miner

List of variants in gene INF2 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP
NM_022489.4(INF2):c.*232G>A rs886050384
NM_022489.4(INF2):c.*815C>T rs886050385
NM_022489.4(INF2):c.-50G>A rs886050379
NM_022489.4(INF2):c.1126A>T (p.Thr376Ser) rs376942822
NM_022489.4(INF2):c.1262_1267CACCCC[3] (p.Pro427_Pro428del) rs573567814
NM_022489.4(INF2):c.1770C>T (p.Pro590=) rs549506051
NM_022489.4(INF2):c.1777G>A (p.Glu593Lys) rs775320095
NM_022489.4(INF2):c.2009A>G (p.Glu670Gly) rs886050381
NM_022489.4(INF2):c.2022A>T (p.Gln674His) rs886050382
NM_022489.4(INF2):c.2201T>G (p.Val734Gly) rs754128624
NM_022489.4(INF2):c.2987C>T (p.Thr996Ile) rs377414980
NM_022489.4(INF2):c.3190T>C (p.Leu1064=) rs886050383
NM_022489.4(INF2):c.3206C>T (p.Pro1069Leu) rs376139171
NM_022489.4(INF2):c.3221G>A (p.Arg1074Lys) rs201445955
NM_022489.4(INF2):c.3550G>A (p.Ala1184Thr) rs374684004
NM_022489.4(INF2):c.459C>G (p.Tyr153Ter) rs754706068
NM_022489.4(INF2):c.966C>T (p.Ala322=) rs774024906
NM_022489.4(INF2):c.986-14A>G rs774186716

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