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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