Product Details

SNP ID
rs5935796
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:14699587 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AACACTTATTTCTTCACCAAATCAT[C/T]TCTTCTAGATATTTTGAAATATACA
Phenotype
MIM: 300515 MIM: 305990
Polymorphism
C/T, Transition 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
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

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