ClinVar Miner

List of variants in gene PIGG reported as likely pathogenic for not provided

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Gene type:
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Total variants: 16
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HGVS dbSNP gnomAD frequency
NM_001127178.3(PIGG):c.1515G>A (p.Trp505Ter) rs150259543 0.00073
NM_001127178.3(PIGG):c.2552A>C (p.Gln851Pro) rs150802299 0.00014
NM_001127178.3(PIGG):c.2180G>A (p.Gly727Glu) rs201842856 0.00005
NM_001127178.3(PIGG):c.2569C>T (p.Gln857Ter) rs1294683568 0.00001
NM_001127178.3(PIGG):c.2625dup (p.Asp876fs) rs1491240980 0.00001
GRCh37/hg19 4p16.3(chr4:499507-502759)x1
NM_001127178.3(PIGG):c.1020del (p.Gly341fs) rs1209087083
NM_001127178.3(PIGG):c.1231C>T (p.Gln411Ter) rs780498908
NM_001127178.3(PIGG):c.1363C>T (p.Gln455Ter)
NM_001127178.3(PIGG):c.1996_2005del (p.Arg666fs) rs1726787605
NM_001127178.3(PIGG):c.2209del (p.Ala737fs) rs2108995799
NM_001127178.3(PIGG):c.2357_2360del (p.Asp786fs) rs1553897582
NM_001127178.3(PIGG):c.2624_2625del (p.Gly874_Leu875insTer) rs771819481
NM_001127178.3(PIGG):c.2736-1G>T rs1731469688
NM_001127178.3(PIGG):c.562del (p.Tyr188fs)
NM_001127178.3(PIGG):c.570+1G>A rs1719513784

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