Product Details
- SNP ID
-
rs200161940
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
2
- Location
-
Chr.1:90714650 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCTCAAAGCTACGCTCCAGTTGATT[A/G]AGCTGGTGGTCGGAAAAAGCTGTCC
- Phenotype
-
MIM: 605212
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
BARHL2
PubMed Links
Gene Details
- Gene
- BARHL2
- Gene Name
- BarH like homeobox 2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_020063.1 |
774 |
Silent Mutation |
CTC,CTT |
L244L |
NP_064447.1 |
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