Product Details

SNP ID
rs190766551
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:138128506 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCAGGAAACATAAAACGTATTTCTC[C/T]TTCCGCAGCAGCAAAGTCATTACTC
Phenotype
MIM: 603575
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
NME5 PubMed Links

Gene Details

Gene
NME5
Gene Name
NME/NM23 family member 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003551.2 414 Missense Mutation AGA,GGA R137G NP_003542.1
XM_005272099.1 414 Missense Mutation AGA,GGA R137G XP_005272156.1
XM_006714716.3 414 Missense Mutation AGA,GGA R137G XP_006714779.1
XM_017009945.1 414 Missense Mutation AGA,GGA R137G XP_016865434.1

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