Product Details

SNP ID
rs115187112
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:34624715 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCTGAAGTAGAAATTTCCAGGGAT[C/T]CCTCAGAGTTATTTGCTAAAATGTT
Phenotype
MIM: 605439
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
EHF PubMed Links

Gene Details

Gene
EHF
Gene Name
ETS homologous factor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001206615.1 Intron NP_001193544.1
NM_001206616.1 Intron NP_001193545.1
NM_012153.5 Intron NP_036285.2
XM_005252857.1 Intron XP_005252914.1
XM_005252860.1 Intron XP_005252917.1
XM_005252861.1 Intron XP_005252918.1
XM_005252862.1 Intron XP_005252919.1
XM_011519983.1 Intron XP_011518285.1
XM_011519984.1 Intron XP_011518286.1
XM_011519985.1 Intron XP_011518287.1
XM_017017534.1 Intron XP_016873023.1

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