Product Details

SNP ID

rs11966402

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:35454765 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCATCCCCCGTCTTTCCCCTTTGG[C/T]TCTGTGCATACTGTTTGGAATCTGT

Phenotype

MIM: 613976

Polymorphism

C/T, 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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