Product Details

SNP ID
rs143942115
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:14874403 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGTACAGTAATTTTGTAAAACATA[C/T]GGAATAACTTATTGTAAATATGGAA
Phenotype
MIM: 300515
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
FANCB PubMed Links

Gene Details

Gene
FANCB
Gene Name
Fanconi anemia complementation group B
There are no transcripts associated with this gene.

Gene
MOSPD2
Gene Name
motile sperm domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001177475.1 Intron NP_001170946.1
NM_152581.3 Intron NP_689794.1
XM_005274451.1 Intron XP_005274508.1

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