ClinVar Miner

List of variants in gene PEX19 studied for abdominal and pelvic region disorder

Included ClinVar conditions (1030):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 94
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HGVS dbSNP
NM_001193644.1(PEX19):c.*2425_*2426CT[2] rs143491060
NM_001193644.1(PEX19):c.-17A>C
NM_002857.3(PEX19):c.*1084T>C rs77962224
NM_002857.3(PEX19):c.*1103C>T rs561417695
NM_002857.3(PEX19):c.*1163T>C rs575199724
NM_002857.3(PEX19):c.*1330G>A rs886045442
NM_002857.3(PEX19):c.*1335G>T rs748536788
NM_002857.3(PEX19):c.*1450T>A rs886045441
NM_002857.3(PEX19):c.*1592G>A rs779471097
NM_002857.3(PEX19):c.*169C>T rs192931972
NM_002857.3(PEX19):c.*172G>C rs886045449
NM_002857.3(PEX19):c.*1745T>C rs186821837
NM_002857.3(PEX19):c.*1761C>A rs761868324
NM_002857.3(PEX19):c.*1790A>G rs886045440
NM_002857.3(PEX19):c.*1852C>G rs370387085
NM_002857.3(PEX19):c.*1980T>C rs372976790
NM_002857.3(PEX19):c.*2057T>G rs56089807
NM_002857.3(PEX19):c.*2068T>C rs536872409
NM_002857.3(PEX19):c.*2155C>T rs886045439
NM_002857.3(PEX19):c.*2156C>G rs10594
NM_002857.3(PEX19):c.*2353G>T rs9853
NM_002857.3(PEX19):c.*2536A>G rs141829599
NM_002857.3(PEX19):c.*2555T>G rs148123121
NM_002857.3(PEX19):c.*2637G>A rs41265787
NM_002857.3(PEX19):c.*2717A>G rs574056299
NM_002857.3(PEX19):c.*328A>G rs115260345
NM_002857.3(PEX19):c.*361G>A rs886045448
NM_002857.3(PEX19):c.*427A>G rs886045447
NM_002857.3(PEX19):c.*469C>T rs886045446
NM_002857.3(PEX19):c.*487T>A rs16831724
NM_002857.3(PEX19):c.*662C>T rs773981843
NM_002857.3(PEX19):c.*77del rs771535781
NM_002857.3(PEX19):c.*854G>A rs747191827
NM_002857.3(PEX19):c.*896A>G rs886045445
NM_002857.3(PEX19):c.*898A>G rs8989
NM_002857.3(PEX19):c.*934A>G rs886045444
NM_002857.3(PEX19):c.*998G>A rs886045443
NM_002857.3(PEX19):c.-14T>G rs2301297
NM_002857.3(PEX19):c.-41C>T rs113442137
NM_002857.3(PEX19):c.-4C>T rs201541204
NM_002857.3(PEX19):c.115C>T (p.Pro39Ser) rs144256391
NM_002857.3(PEX19):c.149C>T (p.Pro50Leu) rs11550117
NM_002857.3(PEX19):c.16G>A (p.Glu6Lys) rs145845197
NM_002857.3(PEX19):c.181-15A>G rs114403769
NM_002857.3(PEX19):c.181-4G>T rs747572423
NM_002857.3(PEX19):c.181-5C>T rs199818690
NM_002857.3(PEX19):c.215A>G (p.Gln72Arg) rs543271441
NM_002857.3(PEX19):c.21C>G (p.Gly7=) rs140039683
NM_002857.3(PEX19):c.254C>T (p.Ala85Val) rs11550119
NM_002857.3(PEX19):c.255G>A (p.Ala85=) rs150928521
NM_002857.3(PEX19):c.261C>T (p.Phe87=) rs146644725
NM_002857.3(PEX19):c.30C>T (p.Val10=) rs144440223
NM_002857.3(PEX19):c.320del (p.Lys107fs) rs1571138735
NM_002857.3(PEX19):c.347-7C>T rs753523567
NM_002857.3(PEX19):c.362C>T (p.Ser121Phe) rs1557854775
NM_002857.3(PEX19):c.402T>C (p.Ser134=) rs139828188
NM_002857.3(PEX19):c.432+2T>C rs757078881
NM_002857.3(PEX19):c.433-11G>T rs41265791
NM_002857.3(PEX19):c.459G>A (p.Leu153=) rs78340311
NM_002857.3(PEX19):c.498T>G (p.Asp166Glu) rs142780305
NM_002857.3(PEX19):c.564G>A (p.Leu188=) rs149058086
NM_002857.3(PEX19):c.630A>C (p.Leu210=) rs202174805
NM_002857.3(PEX19):c.763dup (p.Met255fs) rs267608186
NM_002857.3(PEX19):c.771+3A>G rs141133579
NM_002857.3(PEX19):c.857C>G (p.Ser286Trp) rs149976198
NM_002857.3(PEX19):c.878G>C (p.Gly293Ala) rs139875266
NM_002857.3(PEX19):c.879T>C (p.Gly293=) rs74125561
NM_002857.3(PEX19):c.87C>T (p.Phe29=) rs141911166
NM_002857.4(PEX19):c.*1013G>A
NM_002857.4(PEX19):c.*1069G>A
NM_002857.4(PEX19):c.*1145C>T
NM_002857.4(PEX19):c.*138C>T
NM_002857.4(PEX19):c.*1462C>G
NM_002857.4(PEX19):c.*1471A>T
NM_002857.4(PEX19):c.*1802G>C
NM_002857.4(PEX19):c.*2224G>T
NM_002857.4(PEX19):c.*2383C>G
NM_002857.4(PEX19):c.*2413C>T
NM_002857.4(PEX19):c.*2417C>T
NM_002857.4(PEX19):c.*582G>A
NM_002857.4(PEX19):c.*716C>A
NM_002857.4(PEX19):c.*741C>T
NM_002857.4(PEX19):c.*864C>T
NM_002857.4(PEX19):c.*971G>A
NM_002857.4(PEX19):c.149C>A (p.Pro50His)
NM_002857.4(PEX19):c.272T>C (p.Met91Thr)
NM_002857.4(PEX19):c.346+14A>G
NM_002857.4(PEX19):c.366A>G (p.Gln122=)
NM_002857.4(PEX19):c.40G>C (p.Ala14Pro)
NM_002857.4(PEX19):c.41C>T (p.Ala14Val)
NM_002857.4(PEX19):c.424G>C (p.Asp142His)
NM_002857.4(PEX19):c.536T>G (p.Met179Arg)
NM_002857.4(PEX19):c.594G>C (p.Lys198Asn)
NM_002857.4(PEX19):c.667A>G (p.Ser223Gly)

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