Product Details

SNP ID
rs7757405
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.6:35455712 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
GTCTGCCTTGTGCTCCCTTCAGCCA[A/G]ACACTTAACTGCTTGCTCTCCCTCT
Phenotype
MIM: 613976
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FANCE PubMed Links

Gene Details

Gene
FANCE
Gene Name
Fanconi anemia complementation group E
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_021922.2 Intron NP_068741.1
XM_005248885.2 Intron XP_005248942.1
XM_005248886.2 Intron XP_005248943.1
XM_005248887.2 Intron XP_005248944.1
XM_005248888.3 Intron XP_005248945.1
XM_011514343.2 Intron XP_011512645.1

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