ClinVar Miner

List of variants in gene PIGO reported as likely benign for not specified

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Gene type:
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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_032634.4(PIGO):c.2040G>C (p.Leu680=) rs41274877 0.00511
NM_032634.4(PIGO):c.461C>A (p.Ala154Asp) rs142562923 0.00277
NM_032634.4(PIGO):c.2124G>A (p.Leu708=) rs201657672 0.00095
NM_032634.4(PIGO):c.655+7A>C rs118002220 0.00038
NM_032634.4(PIGO):c.939+12G>C rs370844887 0.00014
NM_032634.4(PIGO):c.2025G>A (p.Ala675=) rs368209276 0.00011
NM_032634.4(PIGO):c.1392C>T (p.Ile464=) rs149790500 0.00006
NM_032634.4(PIGO):c.3141-15C>T rs368599591 0.00006
NM_032634.4(PIGO):c.2910G>A (p.Arg970=) rs1171844461 0.00004
NM_032634.4(PIGO):c.900G>A (p.Leu300=) rs575290480 0.00004
NM_032634.4(PIGO):c.1776C>G (p.Gly592=) rs752370056 0.00003
NM_032634.4(PIGO):c.1935A>G (p.Thr645=) rs138435332 0.00003
NM_032634.4(PIGO):c.2679G>A (p.Ser893=) rs376154801 0.00003
NM_032634.4(PIGO):c.2763C>T (p.Phe921=) rs150780733 0.00003
NM_032634.4(PIGO):c.2854+7C>A rs768338180 0.00003
NM_032634.4(PIGO):c.54C>T (p.Tyr18=) rs773054712 0.00003
NM_032634.4(PIGO):c.939+18C>T rs1173858609 0.00003
NM_032634.4(PIGO):c.2854+10C>T rs535228820 0.00002
NM_032634.4(PIGO):c.2889G>C (p.Leu963=) rs959471469 0.00002
NM_032634.4(PIGO):c.300C>T (p.Phe100=) rs760405794 0.00002
NM_032634.4(PIGO):c.1119+11G>A rs781071758 0.00001
NM_032634.4(PIGO):c.2298G>A (p.Leu766=) rs762673020 0.00001
NM_032634.4(PIGO):c.2316C>T (p.Gly772=) rs761210725 0.00001
NM_032634.4(PIGO):c.459C>T (p.Phe153=) rs201331400 0.00001
NM_032634.4(PIGO):c.512-7C>T rs760113080 0.00001
NM_032634.4(PIGO):c.-2+16_-2+19dup rs1554674000
NM_032634.4(PIGO):c.-26G>T rs911704247
NM_032634.4(PIGO):c.102G>A (p.Glu34=) rs1057523446
NM_032634.4(PIGO):c.1758C>T (p.Val586=) rs144103228
NM_032634.4(PIGO):c.2022G>T (p.Val674=) rs1057522037
NM_032634.4(PIGO):c.2854+8del rs756312077
NM_032634.4(PIGO):c.387C>A (p.Thr129=) rs765968784
NM_032634.4(PIGO):c.511+14A>G rs1554673649
NM_032634.4(PIGO):c.879G>A (p.Glu293=) rs753637423

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