Product Details

SNP ID
rs3087523
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:105361319 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCCCACAGTCGGGGCACAGGATGTC[A/G]TCCCTCTCTGTGAGGAAGCCACGCC
Phenotype
MIM: 602633
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C2orf49 PubMed Links

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 1028 Silent Mutation GAC,GAT D268D NP_001034581.1
NM_001318894.1 1028 Silent Mutation GAC,GAT D268D NP_001305823.1
NM_001318895.1 1028 Silent Mutation GAC,GAT D268D NP_001305824.1
NM_001318896.1 1028 Silent Mutation GAC,GAT D268D NP_001305825.1
NM_001318897.1 1028 Silent Mutation GAC,GAT D154D NP_001305826.1
NM_001318898.1 1028 Silent Mutation GAC,GAT D154D NP_001305827.1
NM_001318899.1 1028 Silent Mutation GAC,GAT D160D NP_001305828.1
NM_001450.3 1028 Silent Mutation GAC,GAT D268D NP_001441.4
NM_201555.1 1028 Silent Mutation GAC,GAT D268D NP_963849.1
NM_201557.3 1028 Silent Mutation GAC,GAT D268D NP_963851.2
XM_011510798.2 1028 Silent Mutation GAC,GAT D268D XP_011509100.1

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