Product Details
- SNP ID
-
rs2287660
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.5:143820501 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- ATAGGTTCTCTGCATGTTTGGAAGT[A/C]GGAATTGGTTGAAGTTGAAGATGAT
- Phenotype
-
MIM: 609961
- Polymorphism
- A/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
HMHB1
PubMed Links
Gene Details
- Gene
- HMHB1
- Gene Name
- histocompatibility minor HB-1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_021182.1 |
166 |
Missense Mutation |
TAG,TCG |
*20S |
NP_067005.1 |
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