Product Details

SNP ID
rs1044083
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:132459028 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AACTGATTGTGAAAGCCATGGGGAT[A/G]GGACTTTAAAACAGCGGTAAGACGC
Phenotype
MIM: 603217
Polymorphism
A/G, 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 2766 UTR 3 NP_001313507.1
NM_001326579.1 2766 UTR 3 NP_001313508.1
NM_001326580.1 2766 Intron NP_001313509.1
NM_003569.2 2766 UTR 3 NP_003560.2
XM_011536178.1 2766 Intron XP_011534480.1

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