ClinVar Miner

List of variants in gene combination ASTN2, TRIM32 reported as likely benign for not provided

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_012210.4(TRIM32):c.-81-291A>G rs114597839 0.00887
NM_012210.4(TRIM32):c.*692C>G rs116058338 0.00526
NM_012210.4(TRIM32):c.*1152A>G rs557939030 0.00190
NM_012210.4(TRIM32):c.558G>C (p.Gln186His) rs117599771 0.00183
NM_012210.4(TRIM32):c.*512A>T rs144172952 0.00160
NM_012210.4(TRIM32):c.1222C>T (p.Arg408Cys) rs3747835 0.00113
NM_012210.4(TRIM32):c.6T>G (p.Ala2=) rs141352486 0.00086
NM_012210.4(TRIM32):c.*1G>A rs142781513 0.00053
NM_012210.4(TRIM32):c.276C>T (p.Ser92=) rs140589523 0.00051
NM_012210.4(TRIM32):c.770C>G (p.Thr257Arg) rs3747834 0.00017
NM_012210.4(TRIM32):c.409C>T (p.Pro137Ser) rs200997003 0.00011
NM_012210.4(TRIM32):c.1416A>G (p.Pro472=) rs374136376 0.00006
NM_012210.4(TRIM32):c.201T>C (p.Ile67=) rs780799984 0.00004
NM_012210.4(TRIM32):c.1191C>G (p.Val397=) rs757752867 0.00003
NM_012210.4(TRIM32):c.370C>T (p.Arg124Trp) rs572052810 0.00002
NM_012210.4(TRIM32):c.375G>A (p.Glu125=) rs780765510 0.00001
NM_012210.4(TRIM32):c.*479G>T rs543534409
NM_012210.4(TRIM32):c.1179T>C (p.Tyr393=) rs1009255684
NM_012210.4(TRIM32):c.1356C>G (p.Leu452=) rs1588217979
NM_012210.4(TRIM32):c.282T>C (p.Ala94=)
NM_012210.4(TRIM32):c.452A>C (p.Glu151Ala)

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