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CACTGACCTCATCTCCTTCTGGCTG[C/T]AGGCAGCTCACAGCTGGGCAGATGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
7 submissions
|
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Phenotype: |
MIM: 605393 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KDM5B 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
|
KDM5B - lysine demethylase 5B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001314042.1 | 5752 | Silent Mutation | CTA,CTG | L,L 1529 | NP_001300971.1 | |
NM_006618.4 | 5752 | Silent Mutation | CTA,CTG | L,L 1493 | NP_006609.3 | |
XM_011509088.2 | 5752 | Silent Mutation | CTA,CTG | L,L 1448 | XP_011507390.1 | |
XM_011509090.2 | 5752 | Silent Mutation | CTA,CTG | L,L 1371 | XP_011507392.1 | |
XM_011509091.2 | 5752 | Silent Mutation | CTA,CTG | L,L 1371 | XP_011507393.1 | |
XM_011509092.2 | 5752 | Silent Mutation | CTA,CTG | L,L 1335 | XP_011507394.1 |