Product Details

SNP ID
rs145070796
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:105361303 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGAATTCAGATGTCTTTCCCACAGT[C/T]GGGGCACAGGATGTCGTCCCTCTCT
Phenotype
MIM: 602633
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
C2orf49 PubMed Links
Additional Information
For this assay, SNP(s) [rs11124029] are located under a probe and SNP(s) [rs3087523] 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
C2orf49
Gene Name
chromosome 2 open reading frame 49
There are no transcripts associated with this gene.

Gene
FHL2
Gene Name
four and a half LIM domains 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001039492.2 1044 Missense Mutation AAC,GAC N274D NP_001034581.1
NM_001318894.1 1044 Missense Mutation AAC,GAC N274D NP_001305823.1
NM_001318895.1 1044 Missense Mutation AAC,GAC N274D NP_001305824.1
NM_001318896.1 1044 Missense Mutation AAC,GAC N274D NP_001305825.1
NM_001318897.1 1044 Missense Mutation AAC,GAC N160D NP_001305826.1
NM_001318898.1 1044 Missense Mutation AAC,GAC N160D NP_001305827.1
NM_001318899.1 1044 Missense Mutation AAC,GAC N166D NP_001305828.1
NM_001450.3 1044 Missense Mutation AAC,GAC N274D NP_001441.4
NM_201555.1 1044 Missense Mutation AAC,GAC N274D NP_963849.1
NM_201557.3 1044 Missense Mutation AAC,GAC N274D NP_963851.2
XM_011510798.2 1044 Missense Mutation AAC,GAC N274D XP_011509100.1

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