In Depth Mutation Analysis: c.569C>T (p.Thr190Ile)
c.569C>T
p.Thr190Ile (144)
Mutation Type:
Polymorphism
Mutation Effect:
Missense
Domain:
Linker
Location:
Exon 6
No. of bases:
1
CpG:
-
Comments:
dbSNP database
No. of patients reported:
1
Patient Information : Show
Residue Information :
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Structural Implications :
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