Product Details

SNP ID
hCV29969676
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:148505942 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGACCAAACTTGAAGAAACCTTTT[G/T]GAGTGTGTGTGTCTGTGTGTGTGTG
Phenotype
MIM: 300806
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
AFF2 PubMed Links

Gene Details

Gene
AFF2
Gene Name
AF4/FMR2 family member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001169122.1 Intron NP_001162593.1
NM_001169123.1 Intron NP_001162594.1
NM_001169124.1 Intron NP_001162595.1
NM_001169125.1 Intron NP_001162596.1
NM_001170628.1 Intron NP_001164099.1
NM_002025.3 Intron NP_002016.2

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