Product Details

SNP ID
rs6759415
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:36699132 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTAACACTTGGAGGTGTGAGCCAAG[C/T]ATCAGCAGCAGTGGGGACAAGACAG
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
VIT PubMed Links

Gene Details

Gene
VIT
Gene Name
vitrin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001177969.1 Intron NP_001171440.1
NM_001177970.1 Intron NP_001171441.1
NM_001177971.1 Intron NP_001171442.1
NM_001177972.1 Intron NP_001171443.1
NM_053276.3 Intron NP_444506.2
XM_011532905.1 Intron XP_011531207.1
XM_011532906.1 Intron XP_011531208.1
XM_017004325.1 Intron XP_016859814.1
XM_017004326.1 Intron XP_016859815.1
XM_017004327.1 Intron XP_016859816.1
XM_017004328.1 Intron XP_016859817.1

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