ClinVar Miner

List of variants reported as other for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 14
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HGVS dbSNP
NM_000137.3(FAH):c.1021C>T (p.Arg341Trp) rs11555096
NM_000169.2(GLA):c.937G>T (p.Asp313Tyr) rs28935490
NM_001122821.2(SET):c.740A>G (p.Glu247Gly) rs768759521
NM_001127208.2(TET2):c.4456T>C (p.Ser1486Pro) rs1553918194
NM_001904.4(CTNNB1):c.121A>G (p.Thr41Ala) rs121913412
NM_001904.4(CTNNB1):c.133_135del (p.Ser45del) rs587776850
NM_001904.4(CTNNB1):c.134C>T (p.Ser45Phe) rs121913409
NM_001904.4(CTNNB1):c.1374A>C (p.Glu458Asp) rs1553631848
NM_001904.4(CTNNB1):c.770C>T (p.Thr257Ile) rs1553630452
NM_001904.4(CTNNB1):c.84_95del (p.Gln28_Asp32delinsHis) rs1553630102
NM_002430.3(MN1):c.912_914GCA[5] (p.Gln309del) rs747503495
NM_003506.4(FZD6):c.346C>T (p.Arg116Ter) rs769116796
NM_005120.3(MED12):c.131G>A (p.Gly44Asp) rs199469672
NM_006015.6(ARID1A):c.6259G>A (p.Gly2087Arg) rs1553153748

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