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AGATATGTCTCTTCATGTGGAGGGC[A/G]AGATGGTCAGACCTGGAAAAACACC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604865 | ||||||||||||||||||||
Literature Links: |
KLF7 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | 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 |
KLF7 - Kruppel like factor 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270942.1 | 1116 | Missense Mutation | TCG,TTG | S,L 227 | NP_001257871.1 | |
NM_001270943.1 | 1116 | Silent Mutation | CTC,CTT | L,L 261 | NP_001257872.1 | |
NM_001270944.1 | 1116 | Silent Mutation | CTC,CTT | L,L 266 | NP_001257873.1 | |
NM_003709.3 | 1116 | Silent Mutation | CTC,CTT | L,L 294 | NP_003700.1 | |
XM_005246926.3 | 1116 | Silent Mutation | CTC,CTT | L,L 295 | XP_005246983.1 | |
XM_006712815.3 | 1116 | Silent Mutation | CTC,CTT | L,L 295 | XP_006712878.1 | |
XM_011512072.2 | 1116 | Silent Mutation | CTC,CTT | L,L 295 | XP_011510374.1 | |
XM_011512073.2 | 1116 | Silent Mutation | CTC,CTT | L,L 264 | XP_011510375.1 | |
XM_011512074.2 | 1116 | Silent Mutation | CTC,CTT | L,L 262 | XP_011510376.1 | |
XM_011512075.1 | 1116 | Intron | XP_011510377.1 | |||
XM_017005161.1 | 1116 | Silent Mutation | CTC,CTT | L,L 294 | XP_016860650.1 | |
XM_017005162.1 | 1116 | Silent Mutation | CTC,CTT | L,L 267 | XP_016860651.1 | |
XM_017005163.1 | 1116 | Intron | XP_016860652.1 | |||
XM_017005164.1 | 1116 | Missense Mutation | TCG,TTG | S,L 227 | XP_016860653.1 |