Product Details

SNP ID

rs12223473

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:59123019 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCATATAATATTTTTTACTTATGTT[G/T]TTCATTTCTGTTGCCATCAGATTCT

Phenotype

MIM: 615584

Polymorphism

G/T, Transversion 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		Intron			NP_001136175.1
NM_001142704.1		Intron			NP_001136176.1
NM_198947.3		Intron			NP_945185.1

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