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SNP ID

rs2783708

Assay Type

Functionally tested

NCBI dbSNP Submissions

14

Location

Chr.1:26159523 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTTCCTGGGACCTTGGAATCTGAC[C/G]CACTGCCAAGGAGACTCCCTGGGAG

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FAM110D PubMed Links

Gene Details

Gene

FAM110D

Gene Name

family with sequence similarity 110 member D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024869.2		Intron			NP_079145.2

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