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TTTCTCATCTCTGTCTTTTTCAGCC[C/T]AGACTGGCAGTGTTTCTGTTGGTAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300286 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KLF8 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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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
|
KLF8 - Kruppel like factor 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001159296.2 | Intron | NP_001152768.1 | ||||
NM_001324099.1 | Intron | NP_001311028.1 | ||||
NM_001324100.1 | Intron | NP_001311029.1 | ||||
NM_001324102.1 | Intron | NP_001311031.1 | ||||
NM_001324104.1 | Intron | NP_001311033.1 | ||||
NM_001324105.1 | Intron | NP_001311034.1 | ||||
NM_007250.5 | Intron | NP_009181.2 | ||||
XM_005261977.2 | Intron | XP_005262034.1 | ||||
XM_005261979.3 | Intron | XP_005262036.1 | ||||
XM_006724575.2 | Intron | XP_006724638.1 | ||||
XM_006724576.3 | Intron | XP_006724639.1 | ||||
XM_011530759.2 | Intron | XP_011529061.1 | ||||
XM_017029250.1 | Intron | XP_016884739.1 |