Product Details

SNP ID
rs7583872
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:152339453 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTACATTAGACACTGCATAATATTA[C/T]TCACTCATTTTTGGCTTGCAGTCAC
Phenotype
MIM: 616285
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
FMNL2 PubMed Links

Gene Details

Gene
FMNL2
Gene Name
formin like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_052905.3 Intron NP_443137.2
XM_005246263.2 Intron XP_005246320.1
XM_005246265.3 Intron XP_005246322.1
XM_011510530.1 Intron XP_011508832.1
XM_011510531.1 Intron XP_011508833.1
XM_011510532.2 Intron XP_011508834.1
XM_011510533.2 Intron XP_011508835.1
XM_011510534.1 Intron XP_011508836.1
XM_011510535.2 Intron XP_011508837.1
XM_011510536.2 Intron XP_011508838.1

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