Product Details

SNP ID
rs117829259
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:107499311 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTTTCTGTCGTGAAAAGAGGATGT[C/G]ATATAGGTTCACCAAAAGTTTATTG
Phenotype
MIM: 613667
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SOBP PubMed Links

Gene Details

Gene
SOBP
Gene Name
sine oculis binding protein homolog
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018013.3 Intron NP_060483.3
XM_005267041.4 Intron XP_005267098.1
XM_005267042.4 Intron XP_005267099.1
XM_011535920.2 Intron XP_011534222.1
XM_011535921.2 Intron XP_011534223.1
XM_011535923.2 Intron XP_011534225.1
XM_017010991.1 Intron XP_016866480.1
XM_017010992.1 Intron XP_016866481.1
XM_017010993.1 Intron XP_016866482.1
XM_017010994.1 Intron XP_016866483.1

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