Product Details

SNP ID
rs17214448
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:75557771 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGCCCCTGCTTCCAGTTCATCGCTC[A/G]TTCACACACACCCTGGGTCTGCCCG
Phenotype
MIM: 614829
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
C4orf26 PubMed Links

Gene Details

Gene
C4orf26
Gene Name
chromosome 4 open reading frame 26
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001206981.1 Intron NP_001193910.1
NM_001257072.1 Intron NP_001244001.1
NM_178497.3 Intron NP_848592.2
XM_011531668.2 Intron XP_011529970.1

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