Product Details

SNP ID
rs79726112
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:24122454 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTGATGCTACACACAAGCTCCGCT[C/T]CTGGATTTTGATGAGGGCTGCACTG
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FAM228B PubMed Links

Gene Details

Gene
FAM228B
Gene Name
family with sequence similarity 228 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145710.1 454 Intron NP_001139182.1
NM_001291328.1 454 Intron NP_001278257.1
Gene
PFN4
Gene Name
profilin family member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_199346.2 454 Missense Mutation NP_955378.1
XM_005264292.2 454 Missense Mutation XP_005264349.1
XM_006712007.3 454 Missense Mutation XP_006712070.1
XM_011532823.2 454 Missense Mutation XP_011531125.1

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