Product Details

SNP ID
rs187042368
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:165210163 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCTTATGGTATGGTTGGAAGCACG[A/G]CCCCAGATTCTCTTTGTGTAAGTGT
Phenotype
MIM: 605774
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
KLHL2 PubMed Links

Gene Details

Gene
KLHL2
Gene Name
kelch like family member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001161521.1 145 Silent Mutation CGA,CGG R7R NP_001154993.1
NM_001161522.1 145 UTR 5 NP_001154994.1
NM_007246.3 145 Intron NP_009177.3
XM_011531572.2 145 Intron XP_011529874.1
XM_011531575.2 145 Intron XP_011529877.1
XM_011531576.2 145 Intron XP_011529878.1
XM_017007674.1 145 Intron XP_016863163.1
XM_017007675.1 145 Intron XP_016863164.1
XM_017007676.1 145 Intron XP_016863165.1
XM_017007677.1 145 Intron XP_016863166.1

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