ClinVar Miner

List of variants reported as benign for connective and soft tissue neoplasm by Illumina Laboratory Services, Illumina

Included ClinVar conditions (55):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 44
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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.*4272C>T rs56708107 0.57619
NM_058172.6(ANTXR2):c.-82C>A rs13140055 0.38249
NM_058172.6(ANTXR2):c.*4056T>A rs11946205 0.31619
NM_058172.6(ANTXR2):c.-319C>G rs11557908 0.18441
NM_058172.6(ANTXR2):c.-410G>A rs72869605 0.18258
NM_058172.6(ANTXR2):c.*1671T>G rs2760 0.11504
NM_003073.5(SMARCB1):c.897G>A (p.Ser299=) rs2229354 0.10948
NM_058172.6(ANTXR2):c.*5602C>G rs4331719 0.10728
NM_058172.6(ANTXR2):c.*28C>T rs61048419 0.08261
NM_003073.5(SMARCB1):c.-117C>T rs11090285 0.08005
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_003073.5(SMARCB1):c.362+7C>T rs34746244 0.00815
NM_058172.6(ANTXR2):c.808G>A (p.Val270Ile) rs113707133 0.00790
NM_058172.6(ANTXR2):c.*5547T>C rs114779758 0.00613
NM_003073.5(SMARCB1):c.438A>G (p.Pro146=) rs35105793 0.00536
NM_003073.5(SMARCB1):c.-31C>T rs34276473 0.00535
NM_058172.6(ANTXR2):c.*1558C>T rs150281545 0.00454
NM_003073.5(SMARCB1):c.-115C>T rs551328283 0.00242
NM_003073.5(SMARCB1):c.628+13C>T rs184021903 0.00235
NM_003073.5(SMARCB1):c.-184G>A rs563943196 0.00165
NM_003073.5(SMARCB1):c.*293C>T rs754865420 0.00051
NM_003073.5(SMARCB1):c.*33T>G rs11541580 0.00034
NM_003073.5(SMARCB1):c.1A>G (p.Met1Val) rs367768260 0.00020
NM_003073.5(SMARCB1):c.-17C>T rs372777519 0.00006
NM_003073.5(SMARCB1):c.1032C>T (p.Gly344=) rs149451748 0.00004
NM_003073.5(SMARCB1):c.978C>T (p.Tyr326=) rs187488637 0.00003
NM_003073.5(SMARCB1):c.*116dup rs397897183
NM_058172.6(ANTXR2):c.*336C>T rs4690108
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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