Product Details

SNP ID
rs76751592
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:56648732 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCTGCCATCTCCTTAGTCTGTGAC[A/G]GATCTGCACTCTGAGGGCAGGCCTT
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_001145459.1 677 Silent Mutation TCC,TCT S70S NP_001138931.1
NM_001145460.1 677 UTR 3 NP_001138932.1
NM_032495.5 677 Silent Mutation TCC,TCT S88S NP_115884.4
NM_139211.4 677 Silent Mutation TCC,TCT S70S NP_631957.1
NM_139212.3 677 Silent Mutation TCC,TCT S70S NP_631958.1
XM_006714052.2 677 Intron XP_006714115.1
XM_017008728.1 677 Silent Mutation TCC,TCT S85S XP_016864217.1
XM_017008729.1 677 Silent Mutation TCC,TCT S70S XP_016864218.1
XM_017008730.1 677 Silent Mutation TCC,TCT S70S XP_016864219.1
XM_017008731.1 677 Silent Mutation TCC,TCT S70S XP_016864220.1
XM_017008732.1 677 Silent Mutation TCC,TCT S70S XP_016864221.1
XM_017008733.1 677 Silent Mutation TCC,TCT S70S XP_016864222.1
XM_017008734.1 677 Silent Mutation TCC,TCT S70S XP_016864223.1

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