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Results for the Protein: NP_891991
33946321
NIN

ninein isoform 5 [Homo sapiens]

Known Diseases associated with this Protein:
  SECKEL SYNDROME 7
2
6
2
6
0
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RefSeq Protein: NP_891991
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Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
dbSNPrs61755995 Polymorphismp.ARG1613CYSN/A
dbSNPrs2295847 Polymorphismp.GLN1934GLUN/A
dbSNPrs12882191 Polymorphismp.GLN1125PRON/A
dbSNPrs2073347 Polymorphismp.GLY1320GLUN/A
dbSNPrs2236316 Polymorphismp.PRO1111ALAN/A
dbSNPrs61742284 Polymorphismp.VAL1152PHEN/A
OMIM608684.0002 Diseasep.ASN1709SERSECKEL SYNDROME 7
OMIM608684.0001 Diseasep.GLN1222ARGSECKEL SYNDROME 7



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