Product Details

SNP ID
rs114890878
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:36361104 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGAGCAATTAACTCAAAAGGATTC[G/T]GGACTTTAAAAAAATCAAGATCACG
Phenotype
MIM: 605255
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
ETV7 PubMed Links

Gene Details

Gene
ETV7
Gene Name
ETS variant 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001207035.1 Intron NP_001193964.1
NM_001207036.1 Intron NP_001193965.1
NM_001207037.1 Intron NP_001193966.1
NM_001207038.1 Intron NP_001193967.1
NM_001207039.1 Intron NP_001193968.1
NM_001207040.1 Intron NP_001193969.1
NM_001207041.1 Intron NP_001193970.1
NM_016135.3 Intron NP_057219.1
XM_011514659.1 Intron XP_011512961.1

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