Product Details

SNP ID
rs139058932
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.10:73376168 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCACCTGCAATCATTGTGCCCAGA[A/G]TCTTCTGATACATCTGAGCGAACAT
Phenotype
MIM: 186360
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
ANXA7 PubMed Links

Gene Details

Gene
ANXA7
Gene Name
annexin A7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001156.4 1469 Missense Mutation ACT,ATT T443I NP_001147.1
NM_001320879.1 1469 Missense Mutation ACT,ATT T403I NP_001307808.1
NM_001320880.1 1469 Missense Mutation ACT,ATT T425I NP_001307809.1
NM_004034.3 1469 Missense Mutation ACT,ATT T465I NP_004025.1
XM_017016162.1 1469 Missense Mutation ACT,ATT T465I XP_016871651.1
XM_017016163.1 1469 Missense Mutation ACT,ATT T443I XP_016871652.1

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