Product Details

SNP ID
rs201649265
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:9025555 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTGTCTTCATCGGAAAAAACTCTG[C/T]CACAAAGGTCTTCAAAGTCCTCAAG
Phenotype
MIM: 300478
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FAM9B PubMed Links

Gene Details

Gene
FAM9B
Gene Name
family with sequence similarity 9 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_205849.3 1459 Missense Mutation GAC,GGC D174G NP_995321.1
XM_011545464.2 1459 Missense Mutation GAC,GGC D174G XP_011543766.1
XM_011545465.2 1459 Intron XP_011543767.1

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