ClinVar Miner

List of variants in gene SERPINA1 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 55
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HGVS dbSNP
NM_000295.4(SERPINA1):c.*1141A>G rs139136785
NM_000295.4(SERPINA1):c.*1195G>A rs886050918
NM_000295.4(SERPINA1):c.*1235C>T rs886050917
NM_000295.4(SERPINA1):c.*1287G>A rs9944155
NM_000295.4(SERPINA1):c.*1292C>T rs78367974
NM_000295.4(SERPINA1):c.*1294T>C rs886050916
NM_000295.4(SERPINA1):c.*1414G>A rs139506803
NM_000295.4(SERPINA1):c.*1494A>T rs781709902
NM_000295.4(SERPINA1):c.*1567C>G rs79555504
NM_000295.4(SERPINA1):c.*172T>C rs886050922
NM_000295.4(SERPINA1):c.*1C>T rs72547410
NM_000295.4(SERPINA1):c.*263C>T rs753776140
NM_000295.4(SERPINA1):c.*400C>T rs886050921
NM_000295.4(SERPINA1):c.*419C>A rs529148469
NM_000295.4(SERPINA1):c.*500G>A rs111349695
NM_000295.4(SERPINA1):c.*678C>T rs151205402
NM_000295.4(SERPINA1):c.*694A>T rs886050920
NM_000295.4(SERPINA1):c.*725G>A rs886050919
NM_000295.4(SERPINA1):c.*792C>T rs139984116
NM_000295.4(SERPINA1):c.-10T>C rs11558258
NM_000295.4(SERPINA1):c.-143C>T rs886050924
NM_000295.4(SERPINA1):c.-176C>T rs756761971
NM_000295.4(SERPINA1):c.-188G>A rs55961721
NM_000295.4(SERPINA1):c.-190G>A rs180723265
NM_000295.4(SERPINA1):c.-191C>T rs886050925
NM_000295.4(SERPINA1):c.-208C>T rs55973910
NM_000295.4(SERPINA1):c.-223A>G rs55967149
NM_000295.4(SERPINA1):c.-7A>G rs559054925
NM_000295.4(SERPINA1):c.-98delC rs202122479
NM_000295.4(SERPINA1):c.1075A>G (p.Lys359Glu) rs200945035
NM_000295.4(SERPINA1):c.1095C>T (p.Asp365=) rs201774333
NM_000295.4(SERPINA1):c.115C>A (p.His39Asn) rs138070585
NM_000295.4(SERPINA1):c.1177C>T (p.Pro393Ser) rs61761869
NM_000295.4(SERPINA1):c.171C>T (p.Phe57=) rs150784949
NM_000295.4(SERPINA1):c.206C>T (p.Ser69Phe) rs199687431
NM_000295.4(SERPINA1):c.211A>C (p.Ser71Arg) rs11575873
NM_000295.4(SERPINA1):c.299T>A (p.Ile100Asn) rs1555369135
NM_000295.4(SERPINA1):c.333T>G (p.Ile111Met) rs886050923
NM_000295.4(SERPINA1):c.436G>A (p.Glu146Lys) rs537285845
NM_000295.4(SERPINA1):c.43C>T (p.Leu15=) rs147283849
NM_000295.4(SERPINA1):c.514G>A (p.Gly172Arg) rs112030253
NM_000295.4(SERPINA1):c.587T>C (p.Leu196Ser) rs368433503
NM_000295.4(SERPINA1):c.608_609AC[1] (p.Thr204Serfs)
NM_000295.4(SERPINA1):c.626T>C (p.Val209Ala) rs1555368958
NM_000295.4(SERPINA1):c.6G>A (p.Pro2=) rs200936638
NM_000295.4(SERPINA1):c.701T>A (p.Val234Glu) rs746197812
NM_000295.4(SERPINA1):c.745G>C (p.Gly249Arg) rs764220898
NM_000295.4(SERPINA1):c.848A>T (p.Lys283Ile) rs864622044
NM_000295.4(SERPINA1):c.875C>T (p.Thr292Ile)
NM_000295.4(SERPINA1):c.880G>A (p.Asp294Asn) rs772436715
NM_000295.4(SERPINA1):c.967C>T (p.Leu323=) rs150455534
NM_001127701.1(SERPINA1):c.17C>T (p.Ser6Leu) rs140814100
NM_001127701.1(SERPINA1):c.236T>A (p.Val79Glu) rs864622047
NM_001127701.1(SERPINA1):c.682G>A (p.Glu228Lys) rs199422208
NM_001127701.1(SERPINA1):c.739C>T (p.Arg247Cys) rs28929470

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