ClinVar Miner

List of variants in gene combination ASTN2, TRIM32 studied for not specified

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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_012210.4(TRIM32):c.1254G>A (p.Val418=) rs1661300 0.10569
NM_012210.4(TRIM32):c.558G>C (p.Gln186His) rs117599771 0.00183
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.770C>G (p.Thr257Arg) rs3747834 0.00017
NM_012210.4(TRIM32):c.366C>G (p.Pro122=) rs137947083 0.00009
NM_012210.4(TRIM32):c.238C>T (p.Leu80=) rs760820148 0.00007
NM_012210.4(TRIM32):c.1662T>C (p.Ser554=) rs372044621 0.00006
NM_012210.4(TRIM32):c.467T>C (p.Leu156Pro) rs145907585 0.00005
NM_012210.4(TRIM32):c.693A>C (p.Ala231=) rs368455215 0.00005
NM_012210.4(TRIM32):c.1134C>T (p.Tyr378=) rs776448126 0.00004
NM_012210.4(TRIM32):c.127A>G (p.Ile43Val) rs764366522 0.00004
NM_012210.4(TRIM32):c.1623G>A (p.Gln541=) rs201083322 0.00004
NM_012210.4(TRIM32):c.501G>A (p.Lys167=) rs200085883 0.00004
NM_012210.4(TRIM32):c.603C>T (p.Arg201=) rs767937527 0.00002
NM_012210.4(TRIM32):c.858T>C (p.Val286=) rs762342489 0.00001
GRCh37/hg19 9q33.1(chr9:119365259-119488641)
GRCh37/hg19 9q33.1(chr9:119378438-119499035)x1
GRCh37/hg19 9q33.1(chr9:119378438-119547311)
GRCh37/hg19 9q33.1(chr9:119387755-119511830)
GRCh37/hg19 9q33.1(chr9:119431587-119475882)x1
GRCh37/hg19 9q33.1(chr9:119445398-119564804)
GRCh37/hg19 9q33.1(chr9:119449856-119510525)
GRCh37/hg19 9q33.1(chr9:119449856-119593736)x1
GRCh37/hg19 9q33.1(chr9:119461795-119539531)
NM_012210.4(TRIM32):c.1068C>T (p.Leu356=) rs1057522634
NM_012210.4(TRIM32):c.1194T>C (p.Phe398=) rs980926202
NM_012210.4(TRIM32):c.1503A>G (p.Gly501=) rs1057524533
NM_012210.4(TRIM32):c.1710G>A (p.Ser570=) rs555217187
NM_012210.4(TRIM32):c.463C>T (p.Arg155Cys) rs374055553
NM_012210.4(TRIM32):c.660G>A (p.Val220=) rs3747833
NM_012210.4(TRIM32):c.699G>C (p.Val233=) rs1057521228
NM_012210.4(TRIM32):c.882T>C (p.Ala294=) rs751714214

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