Product Details

SNP ID
rs199905091
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:218134863 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GATTTCTGGAAAGGTGAAGATCTTA[A/G]TAATTACAGTTACAGCTCTACCCTG
Phenotype
MIM: 146928
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CXCR2 PubMed Links

Gene Details

Gene
CXCR2
Gene Name
C-X-C motif chemokine receptor 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001168298.1 143 Missense Mutation AAT,AGT N21S NP_001161770.1
NM_001557.3 143 Missense Mutation AAT,AGT N21S NP_001548.1
XM_005246530.3 143 Intron XP_005246587.1
XM_017003990.1 143 Missense Mutation AAT,AGT N21S XP_016859479.1
XM_017003991.1 143 Missense Mutation AAT,AGT N21S XP_016859480.1
XM_017003992.1 143 Missense Mutation AAT,AGT N21S XP_016859481.1

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