ClinVar Miner

List of variants in gene INSR reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 12
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NM_000208.4(INSR):c.1080C>T (p.Cys360=) rs56066516
NM_000208.4(INSR):c.1123+13G>T rs72549236
NM_000208.4(INSR):c.190T>C (p.Leu64=) rs144836032
NM_000208.4(INSR):c.2117C>A (p.Ala706Asp) rs142391704
NM_000208.4(INSR):c.2193G>A (p.Thr731=) rs6413501
NM_000208.4(INSR):c.225C>T (p.Asp75=) rs41352749
NM_000208.4(INSR):c.2295C>T (p.Gly765=) rs142654992
NM_000208.4(INSR):c.2971C>A (p.Leu991Ile) rs150114699
NM_000208.4(INSR):c.653-23TC[8] rs3835070
NM_000208.4(INSR):c.653-7_653-6insTC rs1555746860
NM_000208.4(INSR):c.687C>T (p.Thr229=) rs150568177
NM_000208.4(INSR):c.959C>T (p.Thr320Met) rs138528064

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