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TTCTGAATCTGCTCCGTCCCCAACG[C/T]CTTCAGCAAGAGCCCTCTCACTTCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607198 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
EFCAB11 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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EFCAB11 - EF-hand calcium binding domain 11 | ||||||
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There are no transcripts associated with this gene. |
TDP1 - tyrosyl-DNA phosphodiesterase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008744.1 | Intron | NP_001008744.1 | ||||
NM_018319.3 | Intron | NP_060789.2 | ||||
XM_005267847.2 | Intron | XP_005267904.1 | ||||
XM_005267848.2 | Intron | XP_005267905.1 | ||||
XM_006720197.3 | Intron | XP_006720260.1 | ||||
XM_006720198.3 | Intron | XP_006720261.1 | ||||
XM_006720199.1 | Intron | XP_006720262.1 | ||||
XM_011536942.2 | Intron | XP_011535244.1 | ||||
XM_011536943.2 | Intron | XP_011535245.1 | ||||
XM_011536944.1 | Intron | XP_011535246.1 | ||||
XM_017021439.1 | Intron | XP_016876928.1 | ||||
XM_017021440.1 | Intron | XP_016876929.1 | ||||
XM_017021441.1 | Intron | XP_016876930.1 | ||||
XM_017021442.1 | Intron | XP_016876931.1 | ||||
XM_017021443.1 | Intron | XP_016876932.1 | ||||
XM_017021444.1 | Intron | XP_016876933.1 | ||||
XM_017021445.1 | Intron | XP_016876934.1 | ||||
XM_017021446.1 | Intron | XP_016876935.1 |