Product Details

SNP ID
rs143497054
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:33585372 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGCCATCTTGCCTCTTCTGCCACG[A/G]TGGCATCTCTGGGGGTGGAGGTTCG
Phenotype
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
FAM98A PubMed Links

Gene Details

Gene
FAM98A
Gene Name
family with sequence similarity 98 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001304538.1 1102 Missense Mutation CCG,TCG P126S NP_001291467.1
NM_015475.4 1102 Missense Mutation CCG,TCG P321S NP_056290.3

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