Product Details

SNP ID
rs151142608
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:9027964 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTTCTTCTGTTGTTCTTGAAATAT[C/T]CTCTAGAATCCCAAAACAAAATAGT
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 1334 Silent Mutation AGA,AGG R132R NP_995321.1
XM_011545464.2 1334 Silent Mutation AGA,AGG R132R XP_011543766.1
XM_011545465.2 1334 Intron XP_011543767.1

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