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GGACGCAGGCAGGGACCGGTGCGAA[C/T]GGAACACAGGAGCCCGTGTGCCACA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610336 MIM: 605217 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
C2CD4C 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 | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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C2CD4C - C2 calcium dependent domain containing 4C | ||||||
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There are no transcripts associated with this gene. |
SHC2 - SHC adaptor protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012435.2 | Intron | NP_036567.2 | ||||
XM_011527893.2 | Intron | XP_011526195.1 | ||||
XM_011527894.2 | Intron | XP_011526196.1 | ||||
XM_011527895.2 | Intron | XP_011526197.1 | ||||
XM_011527896.2 | Intron | XP_011526198.1 | ||||
XM_017026567.1 | Intron | XP_016882056.1 |
Set Membership: |
HapMap |