Product Details

SNP ID
rs4951301
Assay Type
Functionally tested
NCBI dbSNP Submissions
30
Location
Chr.1:204080085 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTGTGTGGCATAGTAGAGGAAAAGA[A/G]GGAAGAAGTGGGGACAGTATCTCCA
Phenotype
MIM: 604748
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SOX13 PubMed Links

Gene Details

Gene
SOX13
Gene Name
SRY-box 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005686.2 Intron NP_005677.2
XM_005245623.2 Intron XP_005245680.1

View Full Product Details