Product Details

SNP ID
rs1044097
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:105360935 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTGGTCATTACCTTATTGAGTTTA[A/G]AAAACTTTCAAGTTCGTGACATATG
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
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286537.1 1412 Intron NP_001273466.1
NM_024093.2 1412 Intron NP_076998.1
XM_017004892.1 1412 Intron XP_016860381.1
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 1412 UTR 3 NP_001034581.1
NM_001318894.1 1412 UTR 3 NP_001305823.1
NM_001318895.1 1412 UTR 3 NP_001305824.1
NM_001318896.1 1412 UTR 3 NP_001305825.1
NM_001318897.1 1412 UTR 3 NP_001305826.1
NM_001318898.1 1412 UTR 3 NP_001305827.1
NM_001318899.1 1412 UTR 3 NP_001305828.1
NM_001450.3 1412 UTR 3 NP_001441.4
NM_201555.1 1412 UTR 3 NP_963849.1
NM_201557.3 1412 UTR 3 NP_963851.2
XM_011510798.2 1412 UTR 3 XP_011509100.1

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