ClinVar Miner

List of variants in gene GFPT1 reported as likely benign for not provided

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Gene type:
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Total variants: 34
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HGVS dbSNP gnomAD frequency
NC_000002.12:g.69387506A>C rs62135767 0.02324
NM_001244710.2(GFPT1):c.740-252T>A rs116051079 0.01336
NM_001244710.2(GFPT1):c.1726-288T>C rs139890192 0.01306
NM_001244710.2(GFPT1):c.2056-23T>C rs80281016 0.01301
NM_001244710.2(GFPT1):c.8-347G>A rs146059866 0.01297
NM_001244710.2(GFPT1):c.1105+207G>C rs115653599 0.01285
NM_001244710.2(GFPT1):c.115+234A>G rs140840400 0.01167
NM_001244710.2(GFPT1):c.1725+128G>T rs60710948 0.01046
NM_001244710.2(GFPT1):c.223+68dup rs57860122 0.00975
NC_000002.12:g.69387541T>C rs149239600 0.00931
NM_001244710.2(GFPT1):c.1204-111C>T rs187053292 0.00912
NM_001244710.2(GFPT1):c.1482+138A>G rs147508834 0.00866
NM_001244710.2(GFPT1):c.224-55G>A rs146594314 0.00796
NM_001244710.2(GFPT1):c.1894-107G>A rs75839634 0.00728
NM_001244710.2(GFPT1):c.2055+184dup rs61182680 0.00643
NM_001244710.2(GFPT1):c.224-199G>A rs189513089 0.00601
NM_001244710.2(GFPT1):c.115+292T>C rs187026414 0.00488
NM_001244710.2(GFPT1):c.1204-316G>T rs183615424 0.00472
NM_001244710.2(GFPT1):c.549T>C (p.Gly183=) rs144566433 0.00249
NM_001244710.2(GFPT1):c.224-12C>T rs375455794 0.00070
NM_001244710.2(GFPT1):c.45G>A (p.Thr15=) rs763874345 0.00002
NM_001244710.2(GFPT1):c.1009+232_1009+234del rs150762658
NM_001244710.2(GFPT1):c.1010-226_1010-224del rs67630608
NM_001244710.2(GFPT1):c.1010-246del rs927368693
NM_001244710.2(GFPT1):c.1204-253_1204-250dup rs58220809
NM_001244710.2(GFPT1):c.1894-53C>A rs10180609
NM_001244710.2(GFPT1):c.2056-10C>T rs201931307
NM_001244710.2(GFPT1):c.409-10C>T rs1324784114
NM_001244710.2(GFPT1):c.409-8A>T rs982114887
NM_001244710.2(GFPT1):c.420C>G (p.Gly140=) rs1671392979
NM_001244710.2(GFPT1):c.543+175C>G rs58791355
NM_001244710.2(GFPT1):c.544-186_544-185del rs67434964
NM_001244710.2(GFPT1):c.544-199dup rs67434964
NM_001244710.2(GFPT1):c.544-244C>T rs186755099

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