C_355858789_10

• SNP ID: rs779718624
• Gene: FANCB
• Gene Name: Fanconi anemia complementation group B
• Set Membership: -
• Chromosome Location: Chr.X: 14790310 - 14790310 on Build GRCh38
• Polymorphism: A/G, Transition substitution
• Context Sequence [VIC/FAM]:

  AAGGAACAACAAATATTTCATTGTT[A/G]ACTAATGAAATATTCCTGGCAACAG

Assay Details

Species:	Human
dbSNP Submissions:	NA
Phenotype:	MIM: 300515
Literature Links:	FANCB PubMed Links
Allele Nomenclature:
Minor Allele Frequency:

1000Genome	Applied Biosystems^®	HapMap
Global - Not Available	Caucasian - Not Available	CEPH (CEU) - Not Available
EAS - Not Available	African American - Not Available	YRI (Yoruba) - Not Available
SAS - Not Available	Chinese - Not Available	CHB (Han Chinese) - Not Available
AFR - Not Available	Japanese - Not Available	JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available

FANCB - Fanconi anemia complementation group B
Transcript Accession	SNP Location	SNP Type	Observed Codons	Observed Amino Acid	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

More Information

Gene Ontology Categories:

Process(es)

interstrand cross-link repair

Function(s)

protein binding