Product Details

SNP ID
rs141963239
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:27766779 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGTCATGAATAGGACTGTGGTAGA[A/T]GACAGCCAGGTTACAGGAAACTGAA
Phenotype
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
MANSC4 PubMed Links

Gene Details

Gene
MANSC4
Gene Name
MANSC domain containing 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001146221.1 250 Missense Mutation ATC,TTC I84F NP_001139693.1
XM_006719024.3 250 Intron XP_006719087.1
XM_011520542.2 250 Missense Mutation ATC,TTC I57F XP_011518844.1

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