Product Details

SNP ID
rs199550318
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:56650762 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TATCATGGGGGTAGCCTTCTCTTTG[A/G]GGGCTACTTTCTGGGTGCCATATTT
Phenotype
MIM: 607275
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
HOPX PubMed Links

Gene Details

Gene
HOPX
Gene Name
HOP homeobox
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145459.1 779 Intron NP_001138931.1
NM_001145460.1 779 Silent Mutation NP_001138932.1
NM_032495.5 779 Intron NP_115884.4
NM_139211.4 779 Intron NP_631957.1
NM_139212.3 779 Intron NP_631958.1
XM_006714052.2 779 Silent Mutation XP_006714115.1
XM_017008728.1 779 Intron XP_016864217.1
XM_017008729.1 779 Intron XP_016864218.1
XM_017008730.1 779 Intron XP_016864219.1
XM_017008731.1 779 Intron XP_016864220.1
XM_017008732.1 779 Intron XP_016864221.1
XM_017008733.1 779 Intron XP_016864222.1
XM_017008734.1 779 Intron XP_016864223.1

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