Product Details
- SNP ID
-
rs199967021
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.X:73454526 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACTACCTAACACTTTTTTCACCACA[C/T]CATCTGCTGTTCGTGGATTTCAACC
- Phenotype
-
MIM: 300025
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CDX4
PubMed Links
Gene Details
- Gene
- CDX4
- Gene Name
- caudal type homeobox 4
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_005193.1 |
796 |
Missense Mutation |
CCA,TCA |
P266S |
NP_005184.1 |
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