Product Details

SNP ID

rs7009526

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:58011635 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGACCCTGTGAGGCATAAAACCTGA[C/G]CAGTCCTCCCATCTTTGAAGAAAGA

Phenotype

MIM: 611394

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FAM110B PubMed Links

Gene Details

Gene

FAM110B

Gene Name

family with sequence similarity 110 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_147189.2		Intron			NP_671722.1
XM_005251324.2		Intron			XP_005251381.1
XM_005251325.3		Intron			XP_005251382.1
XM_005251326.2		Intron			XP_005251383.1
XM_017013948.1		Intron			XP_016869437.1

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