ClinVar Miner

List of variants in gene SP110 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_004509.4(SP110):c.1100C>T (p.Thr367Met) rs59573011
NM_004509.4(SP110):c.1447G>A (p.Gly483Arg) rs149485401
NM_004509.4(SP110):c.1464C>T (p.Cys488=) rs147355697
NM_004509.4(SP110):c.1591-9C>T rs202101309
NM_004509.4(SP110):c.1650T>C (p.Gly550=) rs35495464
NM_004509.4(SP110):c.1731C>T (p.Cys577=) rs13018234
NM_004509.4(SP110):c.1737G>A (p.Met579Ile) rs3948463
NM_004509.4(SP110):c.1815+14A>G rs34034766

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