Product Details

SNP ID: rs76709099
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:219055182 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGCTTCTGGACCCAGTACAGCAGTT[A/C]CAGGAGGGCAGCGGTGGAGTCCTTT
Phenotype: MIM: 600726
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: IHH PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002181.3	1310	UTR 3			NP_002172.2

There are no transcripts associated with this gene.