Product Details

SNP ID
rs5980062
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:14693439 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGGGATGTGATTACTATAGATATGT[A/C]TACAACGAATAACATGGCCTCAGAA
Phenotype
MIM: 300515 MIM: 305990
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
FANCB PubMed Links

Gene Details

Gene
FANCB
Gene Name
Fanconi anemia complementation group B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001018113.2 Intron NP_001018123.1
NM_001324162.1 Intron NP_001311091.1
NM_152633.3 Intron NP_689846.1
XM_011545470.2 Intron XP_011543772.1
XM_017029355.1 Intron XP_016884844.1
XM_017029356.1 Intron XP_016884845.1
Gene
GLRA2
Gene Name
glycine receptor alpha 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001118885.1 Intron NP_001112357.1
NM_001118886.1 Intron NP_001112358.1
NM_001171942.1 Intron NP_001165413.1
NM_002063.3 Intron NP_002054.1
XM_006724487.3 Intron XP_006724550.1
XM_011545495.2 Intron XP_011543797.1
XM_011545496.2 Intron XP_011543798.1
XM_017029427.1 Intron XP_016884916.1
XM_017029428.1 Intron XP_016884917.1
XM_017029429.1 Intron XP_016884918.1

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