ClinVar Miner

List of variants in gene C19orf12 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP gnomAD frequency
NM_031448.6(C19orf12):c.*2691A>G rs113017735 0.01071
NM_031448.6(C19orf12):c.*3417C>T rs138368723 0.01071
NM_031448.6(C19orf12):c.*3217T>C rs769521665 0.01062
NM_031448.6(C19orf12):c.*791G>A rs111648332 0.01055
NM_031448.6(C19orf12):c.*1880T>C rs112656442 0.01053
NM_031448.6(C19orf12):c.*541G>A rs112752558 0.01053
NM_031448.6(C19orf12):c.*471G>A rs112388598 0.01050
NM_031448.6(C19orf12):c.*814G>A rs112965744 0.01050
NM_031448.6(C19orf12):c.*1592A>G rs113641934 0.01049
NM_031448.6(C19orf12):c.*2956G>T rs113943151 0.00963
NM_031448.6(C19orf12):c.*500G>A rs113415246 0.00186
NM_031448.6(C19orf12):c.*3400T>A rs182700680 0.00162
NM_031448.6(C19orf12):c.313G>A (p.Val105Met) rs146492790 0.00096
NM_031448.6(C19orf12):c.*1226C>T rs775550079 0.00084
NM_031448.6(C19orf12):c.*3242C>T rs886054314 0.00018
NM_031448.6(C19orf12):c.*1897A>T rs528651591 0.00017
NM_031448.6(C19orf12):c.*2222A>C rs535994327 0.00017
NM_031448.6(C19orf12):c.*3745G>A rs140771696 0.00013
NM_031448.6(C19orf12):c.*1488T>G rs777128142 0.00012
NM_031448.6(C19orf12):c.*1595G>A rs537395968 0.00011
NM_031448.6(C19orf12):c.*1827G>C rs761080233 0.00011
NM_031448.6(C19orf12):c.*2449G>A rs746421147 0.00011
NM_031448.6(C19orf12):c.*281C>T rs140718921 0.00011
NM_031448.6(C19orf12):c.*2270T>G rs748603317 0.00010
NM_031448.6(C19orf12):c.*3288T>G rs778264130 0.00010
NM_031448.6(C19orf12):c.68C>T (p.Ala23Val) rs544395324 0.00005
NM_031448.6(C19orf12):c.*2671A>C rs981370297 0.00004
NM_031448.6(C19orf12):c.*3352C>T rs754929270 0.00004
NM_031448.6(C19orf12):c.177G>A (p.Gly59=) rs768063881 0.00004
NM_031448.6(C19orf12):c.*2384C>T rs887855599 0.00003
NM_031448.6(C19orf12):c.*2621C>T rs183432713 0.00003
NM_031448.6(C19orf12):c.*3337G>A rs868247639 0.00003
NM_031448.6(C19orf12):c.*3357G>A rs753828295 0.00003
NM_031448.6(C19orf12):c.*718G>T rs770252476 0.00003
NM_031448.6(C19orf12):c.*1158C>T rs533617895 0.00002
NM_031448.6(C19orf12):c.*1159C>T rs150649006 0.00002
NM_031448.6(C19orf12):c.*1840G>T rs1045611042 0.00002
NM_031448.6(C19orf12):c.*3272C>T rs1455514664 0.00002
NM_031448.6(C19orf12):c.*1037A>G rs886054318 0.00001
NM_031448.6(C19orf12):c.*1178C>A rs886054317 0.00001
NM_031448.6(C19orf12):c.*1453C>T rs886054316 0.00001
NM_031448.6(C19orf12):c.*1648C>T rs1470866753 0.00001
NM_031448.6(C19orf12):c.*1671C>T rs751700304 0.00001
NM_031448.6(C19orf12):c.*1870G>C rs1188670767 0.00001
NM_031448.6(C19orf12):c.*1940T>C rs148675828 0.00001
NM_031448.6(C19orf12):c.*2058T>C rs529341141 0.00001
NM_031448.6(C19orf12):c.*20G>A rs770407188 0.00001
NM_031448.6(C19orf12):c.*2208G>A rs796818328 0.00001
NM_031448.6(C19orf12):c.*2328G>A rs1464022204 0.00001
NM_031448.6(C19orf12):c.*3026G>C rs377009197 0.00001
NM_031448.6(C19orf12):c.*3091A>T rs1175463014 0.00001
NM_031448.6(C19orf12):c.*3294C>G rs886054313 0.00001
NM_031448.6(C19orf12):c.*3300C>T rs1050118432 0.00001
NM_031448.6(C19orf12):c.*3314C>T rs779057343 0.00001
NM_031448.6(C19orf12):c.*3492G>T rs886054312 0.00001
NM_031448.6(C19orf12):c.*3520C>T rs886054311 0.00001
NM_031448.6(C19orf12):c.*3697C>T rs1180327296 0.00001
NM_031448.6(C19orf12):c.*554G>A rs1051290472 0.00001
NM_031448.6(C19orf12):c.*5C>T rs1298758495 0.00001
NM_031448.6(C19orf12):c.-1G>A rs973794044 0.00001
NM_031448.6(C19orf12):c.*1111A>G rs767110273
NM_031448.6(C19orf12):c.*1203A>G rs1972082905
NM_031448.6(C19orf12):c.*1362G>T rs113343769
NM_031448.6(C19orf12):c.*136C>T rs886054321
NM_031448.6(C19orf12):c.*137G>A rs746454120
NM_031448.6(C19orf12):c.*1944A>G rs1972043921
NM_031448.6(C19orf12):c.*2207C>T rs1486513005
NM_031448.6(C19orf12):c.*2373G>T rs76746960
NM_031448.6(C19orf12):c.*2732G>A rs761466058
NM_031448.6(C19orf12):c.*308C>T rs886054320
NM_031448.6(C19orf12):c.*3402dup rs139713991
NM_031448.6(C19orf12):c.*3518C>T rs62105838
NM_031448.6(C19orf12):c.*3672C>T rs886054310
NM_031448.6(C19orf12):c.*437C>T rs1048104
NM_031448.6(C19orf12):c.*466G>A rs886054319
NM_031448.6(C19orf12):c.-10-12T>A rs886054323
NM_031448.6(C19orf12):c.113T>C (p.Met38Thr) rs1972486898
NM_031448.6(C19orf12):c.241C>A (p.Pro81Thr) rs756687848
NM_031448.6(C19orf12):c.371T>C (p.Met124Thr) rs1972169092
NM_031448.6(C19orf12):c.80A>T (p.His27Leu) rs886054322

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