Product Details

SNP ID
rs181756549
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:99547645 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTTTCAATACATCCATCAGACTTG[G/T]TGAAATTTCTTTGGATACCAAAGCT
Phenotype
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
FAM200A PubMed Links

Gene Details

Gene
FAM200A
Gene Name
family with sequence similarity 200 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_145111.3 947 Missense Mutation ACA,CCA T255P NP_659802.1
XM_011515911.2 947 Missense Mutation ACA,CCA T255P XP_011514213.1
XM_011515913.2 947 Missense Mutation ACA,CCA T255P XP_011514215.1

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