Product Details

SNP ID: rs6129731
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:41032047 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GATTGATTTATGTAACTATGAAAAA[A/C]ACTTTAAAAAAAGTAGAAATCAATG
Phenotype: MIM: 126420
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: LOC100128988 PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003286.2		Intron			NP_003277.1