ClinVar Miner

List of variants in gene ANTXR2 reported as benign for bone neoplasm

Included ClinVar conditions (110):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_058172.6(ANTXR2):c.*3695T>C rs4611863 0.98122
NM_058172.6(ANTXR2):c.*1521A>G rs7747 0.80751
NM_058172.6(ANTXR2):c.*784T>G rs1139638 0.80420
NM_058172.6(ANTXR2):c.*785T>C rs63539261 0.80416
NM_058172.6(ANTXR2):c.378+8A>C rs4594664 0.61456
NM_058172.6(ANTXR2):c.636+54T>A rs10745242 0.61408
NM_058172.6(ANTXR2):c.*4272C>T rs56708107 0.57619
NM_058172.6(ANTXR2):c.*4056T>A rs11946205 0.31619
NM_058172.6(ANTXR2):c.-410G>A rs72869605 0.18258
NM_058172.6(ANTXR2):c.*1671T>G rs2760 0.11504
NM_058172.6(ANTXR2):c.*5602C>G rs4331719 0.10728
NM_058172.6(ANTXR2):c.*28C>T rs61048419 0.08261
NM_058172.6(ANTXR2):c.1395G>A (p.Arg465=) rs35798108 0.06853
NM_058172.6(ANTXR2):c.-230_-229del rs80314910 0.06101
NM_058172.6(ANTXR2):c.*1663G>A rs113322831 0.03500
NM_058172.6(ANTXR2):c.*677C>T rs149404014 0.01921
NM_058172.6(ANTXR2):c.-590A>T rs142313419 0.01544
NM_058172.6(ANTXR2):c.225-4G>A rs141355689 0.01410
NM_058172.6(ANTXR2):c.331C>T (p.Arg111Cys) rs61741646 0.01167
NM_058172.6(ANTXR2):c.796+9C>T rs113482034 0.01026
NM_058172.6(ANTXR2):c.808G>A (p.Val270Ile) rs113707133 0.00790
NM_058172.6(ANTXR2):c.*5547T>C rs114779758 0.00613
NM_058172.6(ANTXR2):c.*1558C>T rs150281545 0.00454
NM_058172.6(ANTXR2):c.*336C>T rs4690108
NM_058172.6(ANTXR2):c.1042-114G>A rs4444771
NM_058172.6(ANTXR2):c.1068C>A (p.Pro356=) rs72653288
NM_058172.6(ANTXR2):c.1068C>G (p.Pro356=) rs72653288
NM_058172.6(ANTXR2):c.1069G>C (p.Ala357Pro) rs12647691
NM_058172.6(ANTXR2):c.637-10del rs373672335

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