Product Details

SNP ID
rs116921853
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:93677099 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACAGTATCTTTTCTAAAGTCATATA[C/T]GCAGGTAAGTATTAGTTCTCAGAAA
Phenotype
MIM: 608866
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FRA10AC1 PubMed Links

Gene Details

Gene
FRA10AC1
Gene Name
fragile site, folic acid type, rare, fra(10)(q23.3) or fra(10)(q24.2) candidate 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_145246.4 Intron NP_660289.2
XM_005269515.4 Intron XP_005269572.1
XM_005269516.4 Intron XP_005269573.1
XM_011539259.2 Intron XP_011537561.1
XM_011539260.2 Intron XP_011537562.1
XM_017015656.1 Intron XP_016871145.1
XM_017015657.1 Intron XP_016871146.1
XM_017015658.1 Intron XP_016871147.1
XM_017015659.1 Intron XP_016871148.1
XM_017015660.1 Intron XP_016871149.1
XM_017015661.1 Intron XP_016871150.1
XM_017015662.1 Intron XP_016871151.1

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