ClinVar Miner

List of variants in gene PIGG reported as benign

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Gene type:
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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_001127178.3(PIGG):c.2262-246G>A rs4690277 0.98534
NM_001127178.3(PIGG):c.2261+49A>T rs7697650 0.97007
NM_001127178.3(PIGG):c.571-563A>G rs4690182 0.87699
NM_001127178.3(PIGG):c.*241G>A rs7668455 0.26510
NM_001127178.3(PIGG):c.901+152T>C rs17164861 0.23649
NM_001127178.3(PIGG):c.759+91C>A rs7659929 0.22880
NM_001127178.3(PIGG):c.2571+204T>G rs11934549 0.20165
NM_001127178.3(PIGG):c.1989C>T (p.Ala663=) rs13150531 0.19173
NM_001127178.3(PIGG):c.1828T>C (p.Cys610Arg) rs7666425 0.19169
NM_001127178.3(PIGG):c.1743T>C (p.Leu581=) rs7666226 0.19160
NM_001127178.3(PIGG):c.1615-50G>A rs7678962 0.19122
NM_001127178.3(PIGG):c.1615-285C>G rs7692313 0.19115
NM_001127178.3(PIGG):c.2736-130A>G rs10213020 0.19069
NM_001127178.3(PIGG):c.2795T>C (p.Phe932Ser) rs1127410 0.19048
NM_001127178.3(PIGG):c.2572-188T>C rs11938226 0.18993
NM_001127178.3(PIGG):c.2572-73G>A rs11931692 0.18993
NM_001127178.3(PIGG):c.2572-274T>C rs11938183 0.18992
NM_001127178.3(PIGG):c.2642T>C (p.Ile881Thr) rs34623004 0.18986
NM_001127178.3(PIGG):c.1115-243A>G rs10029096 0.18041
NM_001127178.3(PIGG):c.361-68T>A rs57099085 0.17960
NM_001127178.3(PIGG):c.2095G>A (p.Val699Ile) rs13114026 0.15552
NM_001127178.3(PIGG):c.1373G>A (p.Arg458His) rs13115344 0.13254
NM_001127178.3(PIGG):c.1332+181A>G rs77516519 0.07948
NM_001127178.3(PIGG):c.1115-220C>T rs10024763 0.06896
NM_001127178.3(PIGG):c.2262-210G>A rs79889694 0.06351
NM_001127178.3(PIGG):c.361-232A>T rs868964600 0.04186
NM_001127178.3(PIGG):c.2191G>A (p.Val731Ile) rs34916638 0.03501
NM_001127178.3(PIGG):c.2261+83C>T rs73072152 0.03485
NM_001127178.3(PIGG):c.1615-106T>C rs77489555 0.02651
NM_001127178.3(PIGG):c.990T>C (p.Ser330=) rs11726338 0.02569
NM_001127178.3(PIGG):c.1967C>T (p.Ala656Val) rs61749092 0.01599
NM_001127178.3(PIGG):c.158C>A (p.Ala53Asp) rs28454778 0.00937
NM_001127178.3(PIGG):c.2069+16C>T rs144533568 0.00716
NM_001127178.3(PIGG):c.1520C>T (p.Ala507Val) rs144879126 0.00498
NM_001127178.3(PIGG):c.1930G>A (p.Glu644Lys) rs114931121 0.00498
NM_001127178.3(PIGG):c.759+16G>A rs148792489 0.00426
NM_001127178.3(PIGG):c.771G>A (p.Thr257=) rs35496504 0.00322
NM_001127178.3(PIGG):c.2204G>A (p.Arg735Gln) rs138345843 0.00287
NM_001127178.3(PIGG):c.1114+8A>G rs182522437 0.00233
NM_001127178.3(PIGG):c.1254G>A (p.Thr418=) rs139518242 0.00227
NM_001127178.3(PIGG):c.1581C>T (p.Thr527=) rs143989093 0.00179
NM_001127178.3(PIGG):c.1114+15C>T rs200262444 0.00170
NM_001127178.3(PIGG):c.1114+9A>G rs150974506 0.00159
NM_001127178.3(PIGG):c.902-16G>A rs187291662 0.00157
NM_001127178.3(PIGG):c.2150C>A (p.Ser717Tyr) rs117059276 0.00137
NM_001127178.3(PIGG):c.2085C>T (p.Ala695=) rs150774662 0.00112
NM_001127178.3(PIGG):c.2279G>A (p.Arg760His) rs200170221 0.00022
NM_001127178.3(PIGG):c.588G>A (p.Thr196=) rs149455987 0.00020
NM_001127178.3(PIGG):c.2891T>C (p.Ile964Thr) rs141963092 0.00016
NM_001127178.3(PIGG):c.1594G>C (p.Gly532Arg) rs781714196 0.00012
NM_001127178.3(PIGG):c.2769C>T (p.Tyr923=) rs148579497 0.00012
NM_001127178.3(PIGG):c.361-8G>T rs575862015 0.00004
NM_001127178.3(PIGG):c.883G>T (p.Ala295Ser) rs201853289 0.00004
NM_001127178.3(PIGG):c.1115-216A>G rs10029104
NM_001127178.3(PIGG):c.154+11dup rs782776784
NM_001127178.3(PIGG):c.1614+9G>A rs188737876
NM_001127178.3(PIGG):c.1614+9G>C rs188737876
NM_001127178.3(PIGG):c.164C>A (p.Ser55Tyr) rs34120878
NM_001127178.3(PIGG):c.2069+9G>T rs149305291
NM_001127178.3(PIGG):c.2261+62_2261+63del rs112246308
NM_001127178.3(PIGG):c.2261+64G>T rs112667377
NM_001127178.3(PIGG):c.2571+175C>G rs11931500
NM_001127178.3(PIGG):c.361-69dup rs374663154
NM_001127178.3(PIGG):c.361-70_361-69dup rs374663154
NM_001127178.3(PIGG):c.361-71_361-69dup rs374663154
NM_001127178.3(PIGG):c.759+13G>A rs201035016

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