Product Details

SNP ID
rs202196116
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:59124560 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTCAAGTGCCTGCCTAGTGATTCT[C/T]ATTTTAAAATTACATTTGGTCAAAG
Phenotype
MIM: 615584
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FAM111B PubMed Links

Gene Details

Gene
FAM111B
Gene Name
family with sequence similarity 111 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001142703.1 706 Missense Mutation CAT,TAT H125Y NP_001136175.1
NM_001142704.1 706 Missense Mutation CAT,TAT H125Y NP_001136176.1
NM_198947.3 706 Missense Mutation CAT,TAT H155Y NP_945185.1
Gene
LOC101927204
Gene Name
uncharacterized LOC101927204
There are no transcripts associated with this gene.

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