Product Details
- SNP ID
-
rs10089600
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:16993185 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- CTCTTGGACCTGGCGCCATCTCTTG[C/G]AGTTCCGTCTTTGTTAAGTGCCACA
- Phenotype
-
MIM: 605558
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
FGF20
PubMed Links
Gene Details
- Gene
- FGF20
- Gene Name
- fibroblast growth factor 20
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_019851.2 |
656 |
Missense Mutation |
CCA,GCA |
P175A |
NP_062825.1 |
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