Product Details

SNP ID

rs11769769

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.7:128672396 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TCCCAAGCCCATTCTTACCAAGAAC[C/T]AATGAGTAAAATCAGGGGCCTCCCA

Phenotype

Polymorphism

C/T, 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	131	UTR 5			NP_001012457.3
NM_001128926.3	131	UTR 5			NP_001122398.1
NM_001290254.1	131	UTR 5			NP_001277183.1
NM_001290255.1	131	UTR 5			NP_001277184.1
XM_011516128.2	131	UTR 5			XP_011514430.1
XM_011516129.2	131	UTR 5			XP_011514431.1
XM_011516130.2	131	UTR 5			XP_011514432.1
XM_011516131.2	131	UTR 5			XP_011514433.1
XM_011516132.2	131	UTR 5			XP_011514434.1
XM_011516134.2	131	Intron			XP_011514436.1
XM_011516135.2	131	Intron			XP_011514437.1
XM_011516136.2	131	Intron			XP_011514438.1
XM_017012147.1	131	UTR 5			XP_016867636.1
XM_017012149.1	131	UTR 5			XP_016867638.1

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