Product Details

SNP ID

rs4477177

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:14881290 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGAGGAATGCCTTCATTTTGTTAGG[C/G]TGAAGGAGACAAAGTGGTTAGAGAA

Phenotype

MIM: 300515

Polymorphism

C/G, Transversion 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

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