ClinVar Miner

List of variants reported as likely benign for Pyogenic bacterial infections due to MyD88 deficiency by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_002468.5(MYD88):c.538C>T (p.Arg180Trp) rs201772694 0.00051
NM_002468.5(MYD88):c.645-18C>G rs375012239 0.00021
NM_002468.5(MYD88):c.737-19G>C rs199529701 0.00020
NM_002468.5(MYD88):c.463+8T>G rs776209293 0.00014
NM_002468.5(MYD88):c.329-13C>G rs372702557 0.00009
NM_002468.5(MYD88):c.394G>A (p.Ala132Thr) rs189773684 0.00007
NM_002468.5(MYD88):c.463+11A>T rs369086722 0.00006
NM_002468.5(MYD88):c.66G>T (p.Leu22=) rs765037478 0.00006
NM_002468.5(MYD88):c.669C>G (p.Val223=) rs1241730152 0.00003
NM_002468.5(MYD88):c.831C>T (p.Thr277=) rs1701074174 0.00002
NM_002468.5(MYD88):c.-7G>C rs1023857738 0.00001
NM_002468.5(MYD88):c.114C>T (p.Asn38=) rs867343970 0.00001
NM_002468.5(MYD88):c.396C>T (p.Ala132=) rs554520522 0.00001
NM_002468.5(MYD88):c.464-4C>G rs955933627 0.00001
NM_002468.5(MYD88):c.504C>T (p.Cys168=) rs564072486 0.00001
NM_002468.5(MYD88):c.510C>T (p.Ser170=) rs1415804686 0.00001
NM_002468.5(MYD88):c.564A>T (p.Arg188=) rs748875466 0.00001
NM_002468.5(MYD88):c.636C>T (p.Ile212=) rs765429031 0.00001
NM_002468.5(MYD88):c.645-11C>T rs753676218 0.00001
NM_002468.5(MYD88):c.723C>T (p.Leu241=) rs151334142 0.00001
NM_002468.5(MYD88):c.736+10A>G rs1445955783 0.00001
NM_002468.5(MYD88):c.737-9G>T rs751069957 0.00001
NM_002468.5(MYD88):c.93C>A (p.Arg31=) rs754580369 0.00001
NM_002468.5(MYD88):c.-16T>G
NM_002468.5(MYD88):c.-31C>G
NM_002468.5(MYD88):c.132G>T (p.Ala44=)
NM_002468.5(MYD88):c.156G>A (p.Glu52=) rs1417201017
NM_002468.5(MYD88):c.168T>C (p.Phe56=)
NM_002468.5(MYD88):c.249C>A (p.Gly83=) rs929732833
NM_002468.5(MYD88):c.276G>C (p.Leu92=)
NM_002468.5(MYD88):c.294C>T (p.Arg98=)
NM_002468.5(MYD88):c.313C>T (p.Leu105=)
NM_002468.5(MYD88):c.321C>T (p.Pro107=) rs2125776194
NM_002468.5(MYD88):c.329-15G>A
NM_002468.5(MYD88):c.329-15G>C
NM_002468.5(MYD88):c.329-16T>C
NM_002468.5(MYD88):c.351C>A (p.Ile117=)
NM_002468.5(MYD88):c.363G>A (p.Gln121=)
NM_002468.5(MYD88):c.463+17G>C
NM_002468.5(MYD88):c.464-20C>T
NM_002468.5(MYD88):c.465G>A (p.Gly155=)
NM_002468.5(MYD88):c.483C>T (p.Phe161=)
NM_002468.5(MYD88):c.48C>T (p.Ser16=)
NM_002468.5(MYD88):c.519G>A (p.Gln173=)
NM_002468.5(MYD88):c.525G>A (p.Val175=)
NM_002468.5(MYD88):c.63C>T (p.Pro21=)
NM_002468.5(MYD88):c.644+17C>T
NM_002468.5(MYD88):c.645-14C>T rs760481307
NM_002468.5(MYD88):c.672T>C (p.Ser224=)
NM_002468.5(MYD88):c.682C>T (p.Leu228=)
NM_002468.5(MYD88):c.6T>C (p.Ala2=)
NM_002468.5(MYD88):c.702C>T (p.Asp234=)
NM_002468.5(MYD88):c.729C>T (p.Leu243=)
NM_002468.5(MYD88):c.736+7del
NM_002468.5(MYD88):c.736+9A>T
NM_002468.5(MYD88):c.737-15C>A
NM_002468.5(MYD88):c.737-18G>T rs2125780174
NM_002468.5(MYD88):c.737-8G>A
NM_002468.5(MYD88):c.75C>T (p.Leu25=)
NM_002468.5(MYD88):c.837C>T (p.Pro279=)
NM_002468.5(MYD88):c.883C>T (p.Leu295=)

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