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ACCCAACGGACAGCCCGGGGTTCAA[A/G]ACCTAGCCTTTTTTATGAGATGGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610055 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C19orf57 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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C19orf57 - chromosome 19 open reading frame 57 | ||||||
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There are no transcripts associated with this gene. |
CC2D1A - coiled-coil and C2 domain containing 1A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017721.4 | Intron | NP_060191.3 | ||||
XM_005259972.2 | Intron | XP_005260029.1 | ||||
XM_005259973.2 | Intron | XP_005260030.1 | ||||
XM_005259974.2 | Intron | XP_005260031.1 | ||||
XM_005259975.2 | Intron | XP_005260032.1 |