ClinVar Miner

List of variants in gene LPIN2 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_001375808.2(LPIN2):c.*438C>T rs150379164 0.00868
NM_001375808.2(LPIN2):c.1801G>A (p.Glu601Lys) rs61735393 0.00824
NM_001375808.2(LPIN2):c.*358G>A rs184193388 0.00608
NM_001375808.2(LPIN2):c.1510C>T (p.Leu504Phe) rs104895500 0.00253
NM_001375808.2(LPIN2):c.1735T>C (p.Ser579Pro) rs150022314 0.00221
NM_001375808.2(LPIN2):c.991G>T (p.Ala331Ser) rs80338805 0.00142
NM_001375808.2(LPIN2):c.1159A>G (p.Lys387Glu) rs104895501 0.00083
NM_001375808.2(LPIN2):c.1876C>T (p.Pro626Ser) rs150806357 0.00083
NM_001375808.2(LPIN2):c.1043C>T (p.Pro348Leu) rs34676691 0.00051
NM_001375808.2(LPIN2):c.446C>T (p.Pro149Leu) rs147615538 0.00038
NM_001375808.2(LPIN2):c.2610C>T (p.Ser870=) rs145412418 0.00025
NM_001375808.2(LPIN2):c.2625G>A (p.Pro875=) rs187572602 0.00025
NM_001375808.2(LPIN2):c.1132C>T (p.Pro378Ser) rs201678207 0.00018
NM_001375808.2(LPIN2):c.1904A>G (p.Tyr635Cys) rs747422654 0.00007
NM_001375808.2(LPIN2):c.608C>T (p.Ser203Phe) rs144555528 0.00006
NM_001375808.2(LPIN2):c.1281C>T (p.Pro427=) rs778559792 0.00004
NM_001375808.2(LPIN2):c.1456+4C>G rs373685201 0.00004
NM_001375808.2(LPIN2):c.2316C>T (p.Ser772=) rs145270447 0.00003
NM_001375808.2(LPIN2):c.131A>G (p.Gln44Arg) rs747502342 0.00001
NM_001375808.2(LPIN2):c.1332A>G (p.Pro444=) rs1297660489 0.00001
NM_001375808.2(LPIN2):c.2224G>A (p.Asp742Asn) rs779538504 0.00001
NM_001375808.2(LPIN2):c.2493C>T (p.Thr831=) rs1167923626 0.00001
NM_001375808.2(LPIN2):c.704A>G (p.Tyr235Cys) rs750268013 0.00001
NM_001375808.2(LPIN2):c.*90C>T rs547359065
NM_001375808.2(LPIN2):c.1026G>A (p.Val342=) rs1232642116
NM_001375808.2(LPIN2):c.1169-7del rs746626720
NM_001375808.2(LPIN2):c.146A>G (p.His49Arg) rs1206251835
NM_001375808.2(LPIN2):c.1812C>A (p.Ser604=) rs879254186
NM_001375808.2(LPIN2):c.1830A>C (p.Ser610=)
NM_001375808.2(LPIN2):c.2088-10_2088-8del rs1454496778
NM_001375808.2(LPIN2):c.2621G>T (p.Cys874Phe) rs201160155
NM_001375808.2(LPIN2):c.273G>A (p.Glu91=)
NM_001375808.2(LPIN2):c.501G>C (p.Lys167Asn) rs751939691
NM_001375808.2(LPIN2):c.699C>G (p.Thr233=) rs766689905
NM_001375808.2(LPIN2):c.718T>C (p.Cys240Arg) rs1555675288
NM_001375808.2(LPIN2):c.948C>T (p.Ser316=)

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