Product Details

SNP ID

rs3190233

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:80155429 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCTCAGCGAGGACACGGTGCTTCA[A/C]CCACCCAGTCGCCCTCACCAGAAAT

Phenotype

MIM: 602572

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

ANXA11 PubMed Links

Additional Information

For this assay, SNP(s) [rs76487007] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

ANXA11

Gene Name

annexin A11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001157.2	2498	UTR 3			NP_001148.1
NM_001278407.1	2498	UTR 3			NP_001265336.1
NM_001278408.1	2498	UTR 3			NP_001265337.1
NM_001278409.1	2498	UTR 3			NP_001265338.1
NM_145868.1	2498	UTR 3			NP_665875.1
NM_145869.1	2498	UTR 3			NP_665876.1
XM_005269741.4	2498	UTR 3			XP_005269798.1
XM_005269742.1	2498	Intron			XP_005269799.1
XM_006717813.1	2498	Intron			XP_006717876.1
XM_006717814.3	2498	Intron			XP_006717877.1
XM_011539735.1	2498	Intron			XP_011538037.1
XM_011539736.2	2498	Intron			XP_011538038.1

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