Product Details

SNP ID
rs145972883
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:45230090 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTTGCAAGAGATTTCCTGGTGTTC[A/G]TGAGGCACTGGTGCCCTGGGCCTGG
Phenotype
MIM: 604656
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FMNL1 PubMed Links

Gene Details

Gene
FMNL1
Gene Name
formin like 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005892.3 Intron NP_005883.2
XM_006722062.3 Intron XP_006722125.1
XM_006722063.3 Intron XP_006722126.1
XM_006722064.3 Intron XP_006722127.1
XM_006722065.3 Intron XP_006722128.1
XM_006722066.3 Intron XP_006722129.1
XM_006722069.2 Intron XP_006722132.1
XM_006722070.3 Intron XP_006722133.1
XM_011525179.2 Intron XP_011523481.1
XM_011525180.2 Intron XP_011523482.1
XM_011525182.2 Intron XP_011523484.1

View Full Product Details