Product Details

SNP ID
rs3800202
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:132460072 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CATTTTTAGTAACTACACTTTCCCC[C/T]GTAAACATCAGACTTAAATAGACCA
Phenotype
MIM: 603217
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
STX7 PubMed Links

Gene Details

Gene
STX7
Gene Name
syntaxin 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001326578.1 1722 UTR 3 NP_001313507.1
NM_001326579.1 1722 UTR 3 NP_001313508.1
NM_001326580.1 1722 Intron NP_001313509.1
NM_003569.2 1722 UTR 3 NP_003560.2
XM_011536178.1 1722 Intron XP_011534480.1

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