Product Details

SNP ID
rs4786500
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.16:4475264 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CACCGTGCCCAGCCCTAACTCACTT[C/T]TGAAGTTGCTGCTACTTGCACTGAT
Phenotype
MIM: 141251
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
HMOX2 PubMed Links

Gene Details

Gene
HMOX2
Gene Name
heme oxygenase 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001127204.1 Intron NP_001120676.1
NM_001127205.1 Intron NP_001120677.1
NM_001127206.2 Intron NP_001120678.1
NM_001286267.1 Intron NP_001273196.1
NM_001286268.1 Intron NP_001273197.1
NM_001286269.1 Intron NP_001273198.1
NM_001286270.1 Intron NP_001273199.1
NM_001286271.1 Intron NP_001273200.1
NM_002134.3 Intron NP_002125.3
XM_011522473.1 Intron XP_011520775.1
XM_017023196.1 Intron XP_016878685.1
XM_017023197.1 Intron XP_016878686.1
Gene
NMRAL1
Gene Name
NmrA-like family domain containing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001305141.1 Intron NP_001292070.1
NM_001305142.1 Intron NP_001292071.1
NM_020677.4 Intron NP_065728.1
XM_006720905.3 Intron XP_006720968.1
XM_006720906.2 Intron XP_006720969.1
XM_011522567.2 Intron XP_011520869.1
XM_017023485.1 Intron XP_016878974.1
XM_017023486.1 Intron XP_016878975.1
XM_017023487.1 Intron XP_016878976.1
XM_017023488.1 Intron XP_016878977.1
XM_017023489.1 Intron XP_016878978.1
XM_017023490.1 Intron XP_016878979.1
XM_017023491.1 Intron XP_016878980.1
XM_017023492.1 Intron XP_016878981.1

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