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GAATTCAGATGTCTTTCCCACAGTC[A/G]GGGCACAGGATGTCGTCCCTCTCTG
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602633 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
C2orf49 PubMed Links | |||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | CHB (Han Chinese)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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C2orf49 - chromosome 2 open reading frame 49 | ||||||
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There are no transcripts associated with this gene. |
FHL2 - four and a half LIM domains 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039492.2 | 1043 | Silent Mutation | CCC,CCT | P,P 273 | NP_001034581.1 | |
NM_001318894.1 | 1043 | Silent Mutation | CCC,CCT | P,P 273 | NP_001305823.1 | |
NM_001318895.1 | 1043 | Silent Mutation | CCC,CCT | P,P 273 | NP_001305824.1 | |
NM_001318896.1 | 1043 | Silent Mutation | CCC,CCT | P,P 273 | NP_001305825.1 | |
NM_001318897.1 | 1043 | Silent Mutation | CCC,CCT | P,P 159 | NP_001305826.1 | |
NM_001318898.1 | 1043 | Silent Mutation | CCC,CCT | P,P 159 | NP_001305827.1 | |
NM_001318899.1 | 1043 | Silent Mutation | CCC,CCT | P,P 165 | NP_001305828.1 | |
NM_001450.3 | 1043 | Silent Mutation | CCC,CCT | P,P 273 | NP_001441.4 | |
NM_201555.1 | 1043 | Silent Mutation | CCC,CCT | P,P 273 | NP_963849.1 | |
NM_201557.3 | 1043 | Silent Mutation | CCC,CCT | P,P 273 | NP_963851.2 | |
XM_011510798.2 | 1043 | Silent Mutation | CCC,CCT | P,P 273 | XP_011509100.1 |
Set Membership: |
HapMap |