Product Details

SNP ID

rs2106413

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:14880552 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATAATAGCCTACTTATCTTATTCCT[A/G]ATGATAGAAAGATAGCTCTGAACAT

Phenotype

MIM: 300515

Polymorphism

A/G, 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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