Product Details

SNP ID
rs150742908
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:73376141 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGAAGTCTTCGGTAATCTCCACTC[A/G]TGTCACCTGCAATCATTGTGCCCAG
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 1496 Missense Mutation ACG,ATG T452M NP_001147.1
NM_001320879.1 1496 Missense Mutation ACG,ATG T412M NP_001307808.1
NM_001320880.1 1496 Missense Mutation ACG,ATG T434M NP_001307809.1
NM_004034.3 1496 Missense Mutation ACG,ATG T474M NP_004025.1
XM_017016162.1 1496 Missense Mutation ACG,ATG T474M XP_016871651.1
XM_017016163.1 1496 Missense Mutation ACG,ATG T452M XP_016871652.1

View Full Product Details