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AGCAACCCCAGTTGTGATTACTCTT[C/T]CTTCTGAATTCCTGCAGCACCCATA
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606045 MIM: 603574 | |||||||||||||||||||||||
Literature Links: |
EFCAB12 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 - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
EFCAB12 - EF-hand calcium binding domain 12 | ||||||
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There are no transcripts associated with this gene. |
IFT122 - intraflagellar transport 122 | ||||||
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There are no transcripts associated with this gene. |
MBD4 - methyl-CpG binding domain 4, DNA glycosylase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001276270.1 | Intron | NP_001263199.1 | ||||
NM_001276271.1 | Intron | NP_001263200.1 | ||||
NM_001276272.1 | Intron | NP_001263201.1 | ||||
NM_001276273.1 | Intron | NP_001263202.1 | ||||
NM_003925.2 | Intron | NP_003916.1 | ||||
XM_011513268.2 | Intron | XP_011511570.1 |