Product Details

SNP ID
rs17661191
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:157625551 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CATGTTTAAGTCTCGTGTGAGCTAA[C/T]AGAATCTATGCAATTCTGGAGACTA
Phenotype
MIM: 606698
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SOX30 PubMed Links

Gene Details

Gene
SOX30
Gene Name
SRY-box 30
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001308165.1 2157 Intron NP_001295094.1
NM_007017.2 2157 Intron NP_008948.1
NM_178424.1 2157 Intron NP_848511.1
XM_005265803.4 2157 UTR 3 XP_005265860.1
XM_011534420.1 2157 UTR 3 XP_011532722.1

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