Product Details

SNP ID
rs874898
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:113216619 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTCCTGGAGGTGGTTGGCCTAAAGT[C/G]CTAAGTCTCTACAGCCTCCCTCACC
Phenotype
MIM: 167415
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
PAX8 PubMed Links

Gene Details

Gene
PAX8
Gene Name
paired box 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003466.3 3521 UTR 3 NP_003457.1
NM_013952.3 3521 UTR 3 NP_039246.1
NM_013953.3 3521 UTR 3 NP_039247.1
NM_013992.3 3521 UTR 3 NP_054698.1
XM_011511790.1 3521 UTR 3 XP_011510092.1
XM_011511791.1 3521 UTR 3 XP_011510093.1
XM_011511792.1 3521 UTR 3 XP_011510094.1
XM_011511793.1 3521 UTR 3 XP_011510095.1
XM_011511794.1 3521 UTR 3 XP_011510096.1
XM_017004878.1 3521 Intron XP_016860367.1
XM_017004879.1 3521 Intron XP_016860368.1

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