Product Details

SNP ID
rs9840872
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:39065870 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGATTGGGTAAACGACATTGTACT[C/G]TGTTGTAATGGGAAAACATGTAAGT
Phenotype
MIM: 612167
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
WDR48 PubMed Links

Gene Details

Gene
WDR48
Gene Name
WD repeat domain 48
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001303402.1 289 Intron NP_001290331.1
NM_001303403.1 289 Silent Mutation CTC,CTG L83L NP_001290332.1
NM_020839.3 289 Silent Mutation CTC,CTG L83L NP_065890.1
XM_005265346.3 289 Silent Mutation CTC,CTG L83L XP_005265403.1
XM_011533971.1 289 Silent Mutation CTC,CTG L13L XP_011532273.1
XM_017006960.1 289 Silent Mutation CTC,CTG L13L XP_016862449.1

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