ClinVar Miner

List of variants in gene MYD88 reported as uncertain significance for Pyogenic bacterial infections due to MyD88 deficiency

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 59
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002468.5(MYD88):c.529G>A (p.Glu177Lys) rs145469177 0.00010
NM_002468.5(MYD88):c.322A>G (p.Ser108Gly) rs768726138 0.00007
NM_002468.5(MYD88):c.-9C>G rs587778544 0.00006
NM_002468.5(MYD88):c.366G>T (p.Gln122His) rs372319724 0.00006
NM_002468.5(MYD88):c.860C>T (p.Thr287Ile) rs138284536 0.00006
NM_002468.5(MYD88):c.479G>A (p.Arg160His) rs772707495 0.00005
NM_002468.5(MYD88):c.646T>A (p.Cys216Ser) rs778597415 0.00005
NM_002468.5(MYD88):c.106T>C (p.Phe36Leu) rs372072898 0.00004
NM_002468.5(MYD88):c.499T>C (p.Tyr167His) rs186265242 0.00004
NM_002468.5(MYD88):c.-39A>G rs763199298 0.00003
NM_002468.5(MYD88):c.157G>A (p.Glu53Lys) rs765198848 0.00002
NM_002468.5(MYD88):c.535A>G (p.Ile179Val) rs751552782 0.00002
NM_002468.5(MYD88):c.-26G>T rs1700983375 0.00001
NM_002468.5(MYD88):c.115G>A (p.Val39Met) rs770387646 0.00001
NM_002468.5(MYD88):c.212C>T (p.Thr71Ile) rs761035975 0.00001
NM_002468.5(MYD88):c.328+6G>A rs1701007375 0.00001
NM_002468.5(MYD88):c.38C>G (p.Pro13Arg) rs587778545 0.00001
NM_002468.5(MYD88):c.458C>A (p.Pro153His) rs746846997 0.00001
NM_002468.5(MYD88):c.500A>G (p.Tyr167Cys) rs759979054 0.00001
NM_002468.5(MYD88):c.586C>T (p.Arg196Cys) rs137853064 0.00001
NM_002468.5(MYD88):c.589G>A (p.Asp197Asn) rs775840670 0.00001
NM_002468.5(MYD88):c.751C>T (p.Arg251Ter) rs748659894 0.00001
NM_002468.5(MYD88):c.755T>C (p.Leu252Pro) rs387907272 0.00001
NM_002468.5(MYD88):c.-24_-6del rs746651350
NM_002468.5(MYD88):c.-26G>C rs1700983375
NM_002468.5(MYD88):c.-29A>C
NM_002468.5(MYD88):c.-30G>A rs541535441
NM_002468.5(MYD88):c.-30G>T rs541535441
NM_002468.5(MYD88):c.-8C>G rs1700984625
NM_002468.5(MYD88):c.113A>G (p.Asn38Ser) rs748676192
NM_002468.5(MYD88):c.121A>T (p.Thr41Ser) rs587778543
NM_002468.5(MYD88):c.160A>G (p.Met54Val)
NM_002468.5(MYD88):c.165C>A (p.Asp55Glu) rs1575273881
NM_002468.5(MYD88):c.193G>A (p.Glu65Lys)
NM_002468.5(MYD88):c.250G>A (p.Ala84Thr)
NM_002468.5(MYD88):c.259G>A (p.Gly87Ser)
NM_002468.5(MYD88):c.295G>A (p.Asp99Asn) rs2125776113
NM_002468.5(MYD88):c.31G>A (p.Ala11Thr)
NM_002468.5(MYD88):c.364C>A (p.Gln122Lys) rs772420311
NM_002468.5(MYD88):c.422C>G (p.Thr141Arg) rs1701033534
NM_002468.5(MYD88):c.434C>A (p.Ala145Glu) rs1216607510
NM_002468.5(MYD88):c.434C>T (p.Ala145Val)
NM_002468.5(MYD88):c.455A>T (p.Asp152Val) rs772098418
NM_002468.5(MYD88):c.484G>A (p.Asp162Asn)
NM_002468.5(MYD88):c.511G>A (p.Asp171Asn) rs1559484615
NM_002468.5(MYD88):c.514A>G (p.Ile172Val)
NM_002468.5(MYD88):c.550C>A (p.Gln184Lys)
NM_002468.5(MYD88):c.573G>C (p.Leu191Phe) rs770441444
NM_002468.5(MYD88):c.587G>A (p.Arg196His)
NM_002468.5(MYD88):c.602G>A (p.Gly201Asp) rs1701052219
NM_002468.5(MYD88):c.62C>G (p.Pro21Arg) rs563686976
NM_002468.5(MYD88):c.653G>A (p.Arg218Gln)
NM_002468.5(MYD88):c.657G>A (p.Met219Ile)
NM_002468.5(MYD88):c.664G>C (p.Val222Leu)
NM_002468.5(MYD88):c.683T>G (p.Leu228Arg)
NM_002468.5(MYD88):c.700G>A (p.Asp234Asn)
NM_002468.5(MYD88):c.754C>G (p.Leu252Val) rs1575278069
NM_002468.5(MYD88):c.838T>G (p.Cys280Gly) rs1156691174
NM_002468.5(MYD88):c.851G>A (p.Trp284Ter)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.