Product Details
- SNP ID
-
rs137856773
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:20447843 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AAAAAGACCTGCGCAGCGACGAGCA[G/T]GTCCGCACAGAGCTGGCCCGCATGA
- Phenotype
-
MIM: 165370
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
RHOB
PubMed Links
Gene Details
- Gene
- RHOB
- Gene Name
- ras homolog family member B
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_004040.3 |
773 |
Missense Mutation |
CAG,CAT |
Q126H |
NP_004031.1 |
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