Product Details

SNP ID

rs138558402

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:59109664 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGACTGAAGAAAACAAGTCATTTAG[C/T]GCTATGGAAGATGACCAGAGGACTA

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	282	Intron			NP_001136175.1
NM_001142704.1	282	Intron			NP_001136176.1
NM_198947.3	282	Silent Mutation	AGC,AGT	S13S	NP_945185.1

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