Product Details

SNP ID: rs2229989
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:72122794 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGCGCGTGCAGCACAAGAAGGACCA[C/T]CCGGATTACAAGTACCAGCCGCGGC
Phenotype: MIM: 608160
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: SOX9 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000346.3	879	Silent Mutation	CAC,CAT	H169H	NP_000337.1

There are no transcripts associated with this gene.