Product Details

SNP ID
rs11190680
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:100746058 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACAGTGGCAAGTTGCGGCTACTGC[A/G]GTTGCAAGCTCCGGCCAACCCGGAG
Phenotype
MIM: 167409
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
PAX2 PubMed Links

Gene Details

Gene
PAX2
Gene Name
paired box 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000278.4 348 UTR 5 NP_000269.3
NM_001304569.1 348 Intron NP_001291498.1
NM_003987.4 348 UTR 5 NP_003978.3
NM_003988.4 348 UTR 5 NP_003979.2
NM_003989.4 348 UTR 5 NP_003980.3
NM_003990.4 348 UTR 5 NP_003981.3
XM_017016281.1 348 Intron XP_016871770.1
XM_017016282.1 348 Intron XP_016871771.1
XM_017016283.1 348 Intron XP_016871772.1
XM_017016284.1 348 Intron XP_016871773.1
XM_017016285.1 348 Intron XP_016871774.1
XM_017016286.1 348 Intron XP_016871775.1
XM_017016287.1 348 Intron XP_016871776.1
XM_017016288.1 348 Intron XP_016871777.1
XM_017016289.1 348 Intron XP_016871778.1

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