ClinVar Miner

List of variants in gene FECH reported as benign

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Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_000140.5(FECH):c.*2526T>C rs2723680 0.99842
NM_000140.5(FECH):c.*2825A>G rs8090261 0.99840
NM_000140.5(FECH):c.314+23A>G rs577152 0.98504
NM_000140.5(FECH):c.*4563G>T rs663774 0.76588
NM_000140.5(FECH):c.921A>G (p.Pro307=) rs536560 0.74784
NM_000140.5(FECH):c.705+211A>G rs1736439 0.59106
NM_000140.5(FECH):c.804+123A>G rs1736440 0.59036
NM_000140.5(FECH):c.599-255G>A rs3817726 0.58495
NM_000140.5(FECH):c.706-198T>C rs1646594 0.52341
NM_000140.5(FECH):c.315-279T>G rs71355627 0.26978
NM_000140.5(FECH):c.*4886T>G rs7238897 0.26760
NM_000140.5(FECH):c.*248C>T rs8339 0.21849
NM_000140.5(FECH):c.912+94T>A rs28617328 0.15827
NM_000140.5(FECH):c.195-111A>G rs35655063 0.14186
NM_000140.5(FECH):c.194+187G>A rs71355630 0.11943
NM_000140.5(FECH):c.*3377G>T rs480942 0.11174
NM_000140.5(FECH):c.287G>A (p.Arg96Gln) rs1041951 0.10933
NM_000140.5(FECH):c.*2371T>G rs1062010 0.10588
NM_000140.5(FECH):c.1138-61G>A rs12957678 0.10159
NM_000140.5(FECH):c.1077+117_1077+123del rs58628398 0.10154
NM_000140.5(FECH):c.913-62_913-61del rs60626363 0.10134
NM_000140.5(FECH):c.804+263A>G rs9956673 0.10093
NM_000140.5(FECH):c.464-299A>T rs58442256 0.09634
NM_000140.5(FECH):c.598+301G>A rs2269222 0.08954
NM_000140.5(FECH):c.1077+252T>C rs72627248 0.08211
NM_000140.5(FECH):c.913-43A>C rs28451199 0.04371
NM_000140.5(FECH):c.599-112C>G rs9963013 0.04274
NM_000140.5(FECH):c.194+306C>T rs73436947 0.03650
NM_000140.5(FECH):c.*2739T>C rs111695226 0.03343
NM_000140.5(FECH):c.804+279T>C rs111761849 0.03163
NM_000140.5(FECH):c.*4463A>G rs7228449 0.03133
NM_000140.5(FECH):c.*3601A>G rs73453635 0.02742
NM_000140.5(FECH):c.194+43C>T rs61202988 0.02500
NM_000140.5(FECH):c.*117C>T rs8099115 0.02200
NM_000140.5(FECH):c.*4971A>G rs114530851 0.02076
NM_000140.5(FECH):c.*2451T>G rs55769459 0.01725
NM_000140.5(FECH):c.*1622T>C rs78359676 0.01713
NM_000140.5(FECH):c.*696C>T rs76175837 0.01710
NM_000140.5(FECH):c.*422T>A rs3760612 0.01705
NM_000140.5(FECH):c.*481A>G rs3760613 0.01701
NM_000140.5(FECH):c.*5588G>A rs78224804 0.01585
NM_000140.5(FECH):c.*4106A>G rs72940306 0.00744
NM_000140.5(FECH):c.463+43C>T rs73959100 0.00654
NM_000140.5(FECH):c.1077+35C>T rs77695117 0.00243
NM_000140.5(FECH):c.183A>G (p.Gln61=) rs76286732 0.00177
NM_000140.5(FECH):c.705+19G>C rs202119041 0.00176
NM_000140.5(FECH):c.598+12T>A rs370521491 0.00071
NM_000140.5(FECH):c.514G>A (p.Glu172Lys) rs200650502 0.00001
NM_000140.5(FECH):c.*1287_*1288insTA rs59569925
NM_000140.5(FECH):c.*2461dup rs529946604
NM_000140.5(FECH):c.*4891dup rs146687823
NM_000140.5(FECH):c.*5628C>A rs13732
NM_000140.5(FECH):c.1078-51del rs57800921
NM_000140.5(FECH):c.163G>A (p.Gly55Ser) rs3848519
NM_000140.5(FECH):c.163G>T (p.Gly55Cys) rs3848519
NM_000140.5(FECH):c.291C>T (p.Asp97=) rs577947755
NM_000140.5(FECH):c.384C>T (p.Gly128=)
NM_000140.5(FECH):c.798C>G (p.Pro266=) rs536765
NM_000140.5(FECH):c.804+217dup rs3216687
NM_000140.5(FECH):c.913-7C>T rs369538477
NM_000140.5(FECH):c.949G>A (p.Glu317Lys)

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