ClinVar Miner

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

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_004509.3(SP110):c.1038G>C (p.Ser346=) rs7606916
NM_004509.3(SP110):c.1100C>T (p.Thr367Met) rs59573011
NM_004509.3(SP110):c.1274C>T (p.Ser425Leu) rs3948464
NM_004509.3(SP110):c.1447G>A (p.Gly483Arg) rs149485401
NM_004509.3(SP110):c.1568T>C (p.Met523Thr) rs1135791
NM_004509.3(SP110):c.1647C>T (p.Cys549=) rs116626378
NM_080424.2(SP110):c.*206_*207insAATTAA rs5839361
NM_080424.2(SP110):c.1591-9C>T rs202101309

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