ClinVar Miner

List of variants in gene combination ASTN2, TRIM32 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (902):
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Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP
NC_000009.11:g.(?_119460012)_(119461993_?)dup
NM_001365068.1(ASTN2):c.2806+24577T>G rs886063388
NM_001365068.1(ASTN2):c.2806+24653_2806+24656dup rs758130716
NM_001365068.1(ASTN2):c.2806+24860T>C rs886063386
NM_001365068.1(ASTN2):c.2806+24990G>A rs41266677
NM_001365068.1(ASTN2):c.2806+25007A>G rs886063385
NM_001365068.1(ASTN2):c.2806+25132T>C rs886063384
NM_001365068.1(ASTN2):c.2806+25201T>G rs886063383
NM_001365068.1(ASTN2):c.2806+25258del rs886063382
NM_001365068.1(ASTN2):c.2806+25330A>G rs549857802
NM_001365068.1(ASTN2):c.2806+25375G>C rs116058338
NM_001365068.1(ASTN2):c.2806+25478C>T rs16933835
NM_001365068.1(ASTN2):c.2806+25555T>A rs144172952
NM_001365068.1(ASTN2):c.2806+25588C>A rs543534409
NM_001365068.1(ASTN2):c.2806+25784C>A rs886063381
NM_001365068.1(ASTN2):c.2806+25890G>A rs149956877
NM_001365068.1(ASTN2):c.2806+25915A>C rs868402796
NM_001365068.1(ASTN2):c.2806+25955C>T rs886063380
NM_001365068.1(ASTN2):c.2806+25983T>G rs571526516
NM_012210.3(TRIM32):c.-109T>C rs886063378
NM_012210.3(TRIM32):c.-124G>A rs752864284
NM_012210.3(TRIM32):c.1004G>A (p.Ser335Asn) rs778321975
NM_012210.3(TRIM32):c.1012G>A (p.Ala338Thr) rs141806013
NM_012210.3(TRIM32):c.1039G>C (p.Glu347Gln) rs1564217118
NM_012210.3(TRIM32):c.1042G>T (p.Ala348Ser)
NM_012210.3(TRIM32):c.1046C>G (p.Ala349Gly) rs774316527
NM_012210.3(TRIM32):c.1168C>T (p.Arg390Cys) rs754554333
NM_012210.3(TRIM32):c.1181G>A (p.Arg394His) rs121434447
NM_012210.3(TRIM32):c.1196C>T (p.Thr399Ile) rs1182257457
NM_012210.3(TRIM32):c.1223G>A (p.Arg408His) rs183136193
NM_012210.3(TRIM32):c.1225C>T (p.Arg409Cys)
NM_012210.3(TRIM32):c.1226G>A (p.Arg409His) rs145828717
NM_012210.3(TRIM32):c.1354C>T (p.Leu452Phe) rs747067557
NM_012210.3(TRIM32):c.1384G>A (p.Val462Met) rs772922696
NM_012210.3(TRIM32):c.1386G>A (p.Val462=) rs762905941
NM_012210.3(TRIM32):c.1432T>G (p.Leu478Val) rs371002754
NM_012210.3(TRIM32):c.1488C>G (p.Phe496Leu)
NM_012210.3(TRIM32):c.1619G>A (p.Arg540Gln)
NM_012210.3(TRIM32):c.1642G>A (p.Gly548Ser)
NM_012210.3(TRIM32):c.164G>T (p.Ser55Ile) rs1564215128
NM_012210.3(TRIM32):c.1685del (p.Gly562fs) rs1564218190
NM_012210.3(TRIM32):c.1688G>A (p.Arg563His) rs138056275
NM_012210.3(TRIM32):c.1720G>T (p.Asp574Tyr) rs886063379
NM_012210.3(TRIM32):c.1757G>T (p.Arg586Leu)
NM_012210.3(TRIM32):c.1838G>A (p.Arg613Gln) rs199704873
NM_012210.3(TRIM32):c.1857G>A (p.Pro619=)
NM_012210.3(TRIM32):c.1882G>A (p.Gly628Arg) rs1360716233
NM_012210.3(TRIM32):c.1930A>G (p.Ser644Gly) rs1462453134
NM_012210.3(TRIM32):c.1954A>G (p.Thr652Ala) rs763172140
NM_012210.3(TRIM32):c.257T>C (p.Ile86Thr) rs200326473
NM_012210.3(TRIM32):c.27G>C (p.Leu9=) rs201891227
NM_012210.3(TRIM32):c.292C>A (p.Leu98Ile) rs201877419
NM_012210.3(TRIM32):c.316C>T (p.Arg106Cys) rs1390593037
NM_012210.3(TRIM32):c.330A>G (p.Gln110=) rs770015462
NM_012210.3(TRIM32):c.337C>T (p.Arg113Trp) rs762785784
NM_012210.3(TRIM32):c.370C>T (p.Arg124Trp) rs572052810
NM_012210.3(TRIM32):c.377C>T (p.Ala126Val)
NM_012210.3(TRIM32):c.404C>T (p.Thr135Ile) rs141953092
NM_012210.3(TRIM32):c.409C>T (p.Pro137Ser) rs200997003
NM_012210.3(TRIM32):c.43C>T (p.Arg15Trp)
NM_012210.3(TRIM32):c.440G>A (p.Arg147Gln) rs552938001
NM_012210.3(TRIM32):c.464G>A (p.Arg155His) rs777914761
NM_012210.3(TRIM32):c.479T>C (p.Met160Thr)
NM_012210.3(TRIM32):c.479T>G (p.Met160Arg)
NM_012210.3(TRIM32):c.480G>A (p.Met160Ile) rs200196832
NM_012210.3(TRIM32):c.488T>C (p.Leu163Pro)
NM_012210.3(TRIM32):c.496C>T (p.Arg166Trp) rs752016708
NM_012210.3(TRIM32):c.497G>A (p.Arg166Gln) rs759945386
NM_012210.3(TRIM32):c.521C>T (p.Ser174Phe) rs138699534
NM_012210.3(TRIM32):c.688A>G (p.Ile230Val)
NM_012210.3(TRIM32):c.69C>T (p.Cys23=) rs575633576
NM_012210.3(TRIM32):c.700C>A (p.Gln234Lys) rs886043553
NM_012210.3(TRIM32):c.770C>G (p.Thr257Arg) rs3747834
NM_012210.3(TRIM32):c.812G>A (p.Arg271Gln)
NM_012210.3(TRIM32):c.863C>A (p.Pro288His)
NM_012210.3(TRIM32):c.873T>G (p.Ile291Met) rs766687896
NM_012210.3(TRIM32):c.875G>A (p.Gly292Glu) rs1554732992
NM_012210.3(TRIM32):c.889A>G (p.Lys297Glu)
NM_012210.3(TRIM32):c.907G>A (p.Val303Met) rs144532174
NM_012210.3(TRIM32):c.986C>T (p.Pro329Leu) rs377510422

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