ClinVar Miner

List of variants reported as benign for Hyaline fibromatosis syndrome by Illumina Clinical Services Laboratory,Illumina

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Total variants: 29
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HGVS dbSNP
NM_058172.6(ANTXR2):c.*1521A>G rs7747
NM_058172.6(ANTXR2):c.*1558C>T rs150281545
NM_058172.6(ANTXR2):c.*1663G>A rs113322831
NM_058172.6(ANTXR2):c.*1671T>G rs2760
NM_058172.6(ANTXR2):c.*28C>T rs61048419
NM_058172.6(ANTXR2):c.*336C>T rs4690108
NM_058172.6(ANTXR2):c.*3695T>C rs4611863
NM_058172.6(ANTXR2):c.*4056T>A rs11946205
NM_058172.6(ANTXR2):c.*4272C>T rs56708107
NM_058172.6(ANTXR2):c.*5547T>C rs114779758
NM_058172.6(ANTXR2):c.*5602C>G rs4331719
NM_058172.6(ANTXR2):c.*677C>T rs149404014
NM_058172.6(ANTXR2):c.*784T>G rs1139638
NM_058172.6(ANTXR2):c.*785T>C rs63539261
NM_058172.6(ANTXR2):c.-230_-229del rs80314910
NM_058172.6(ANTXR2):c.-319C>G rs11557908
NM_058172.6(ANTXR2):c.-410G>A rs72869605
NM_058172.6(ANTXR2):c.-590A>T rs142313419
NM_058172.6(ANTXR2):c.-82C>A rs13140055
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.1395G>A (p.Arg465=) rs35798108
NM_058172.6(ANTXR2):c.225-4G>A rs141355689
NM_058172.6(ANTXR2):c.331C>T (p.Arg111Cys) rs61741646
NM_058172.6(ANTXR2):c.378+8A>C rs4594664
NM_058172.6(ANTXR2):c.637-10del rs373672335
NM_058172.6(ANTXR2):c.796+9C>T rs113482034
NM_058172.6(ANTXR2):c.808G>A (p.Val270Ile) rs113707133

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