Product Details

SNP ID
rs4368273
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:17750209 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCTGTGTAACCTTGGGCAAGTCTCC[A/G]GCCATCTCTGGGCTTTGTGCTGGTA
Phenotype
MIM: 613437
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FCHO1 PubMed Links

Gene Details

Gene
FCHO1
Gene Name
FCH domain only 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001161357.1 Intron NP_001154829.1
NM_001161358.1 Intron NP_001154830.1
NM_001161359.1 Intron NP_001154831.1
NM_015122.2 Intron NP_055937.1
XM_005259831.3 Intron XP_005259888.1
XM_006722701.3 Intron XP_006722764.1
XM_006722702.3 Intron XP_006722765.1
XM_011527824.2 Intron XP_011526126.1
XM_011527825.2 Intron XP_011526127.1
XM_011527826.2 Intron XP_011526128.1
XM_011527827.2 Intron XP_011526129.1
XM_011527828.2 Intron XP_011526130.1
XM_017026519.1 Intron XP_016882008.1
XM_017026520.1 Intron XP_016882009.1
XM_017026521.1 Intron XP_016882010.1
XM_017026522.1 Intron XP_016882011.1
XM_017026523.1 Intron XP_016882012.1
XM_017026524.1 Intron XP_016882013.1
XM_017026525.1 Intron XP_016882014.1
XM_017026526.1 Intron XP_016882015.1
XM_017026527.1 Intron XP_016882016.1
XM_017026528.1 Intron XP_016882017.1

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