Product Details

SNP ID

rs10239393

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:128673138 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCCTCTAGCGGTCTAGCCTGAACCC[A/G]TGCTCCTGCGCAGGAGAGCATAACC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM71F2 PubMed Links

Gene Details

Gene

FAM71F2

Gene Name

family with sequence similarity 71 member F2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012454.5		Intron			NP_001012457.3
NM_001128926.3		Intron			NP_001122398.1
NM_001290254.1		Intron			NP_001277183.1
NM_001290255.1		Intron			NP_001277184.1
XM_011516128.2		Intron			XP_011514430.1
XM_011516129.2		Intron			XP_011514431.1
XM_011516130.2		Intron			XP_011514432.1
XM_011516131.2		Intron			XP_011514433.1
XM_011516132.2		Intron			XP_011514434.1
XM_011516134.2		Intron			XP_011514436.1
XM_011516135.2		Intron			XP_011514437.1
XM_011516136.2		Intron			XP_011514438.1
XM_017012147.1		Intron			XP_016867636.1
XM_017012149.1		Intron			XP_016867638.1

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