Product Details
- SNP ID
-
rs200122905
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:44264876 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTGTCATGTGGCCCAGGAAATGGCC[G/T]CACTGTGCTCCTTGGCCTTCATGCG
- Phenotype
-
MIM: 605420
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
ALX4
PubMed Links
Gene Details
- Gene
- ALX4
- Gene Name
- ALX homeobox 4
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_021926.3 |
1318 |
Missense Mutation |
GGG,GTG |
G405V |
NP_068745.2 |
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