Product Details

SNP ID
rs1047042
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:55146212 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCAAGAACTGGGGAAAGTTTGCAT[T/C]GGGTTCAGTAACAATCTGGTTTAAG
Phenotype
Polymorphism
T/C, Transition substitution
Allele Nomenclature
Literature Links
FAM104B PubMed Links

Gene Details

Gene
FAM104B
Gene Name
family with sequence similarity 104 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001166699.1 259 Missense Mutation NP_001160171.1
NM_001166700.1 259 Missense Mutation NP_001160172.1
NM_001166701.1 259 Missense Mutation NP_001160173.1
NM_001166702.1 259 Missense Mutation NP_001160174.1
NM_001166703.1 259 Missense Mutation NP_001160175.1
NM_001166704.1 259 UTR 3 NP_001160176.1
NM_138362.3 259 Missense Mutation NP_612371.2
XM_017029951.1 259 Missense Mutation XP_016885440.1
XM_017029952.1 259 Missense Mutation XP_016885441.1
XM_017029953.1 259 Missense Mutation XP_016885442.1

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