Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300128 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KDM6A 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
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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KDM6A - lysine demethylase 6A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001291415.1 | 465 | Missense Mutation | ACG,GCG | T,A 30 | NP_001278344.1 | |
NM_001291416.1 | 465 | Missense Mutation | ACG,GCG | T,A 30 | NP_001278345.1 | |
NM_001291417.1 | 465 | Missense Mutation | ACG,GCG | T,A 30 | NP_001278346.1 | |
NM_001291418.1 | 465 | Missense Mutation | ACG,GCG | T,A 30 | NP_001278347.1 | |
NM_001291421.1 | 465 | UTR 5 | NP_001278350.1 | |||
NM_021140.3 | 465 | Missense Mutation | ACG,GCG | T,A 30 | NP_066963.2 | |
XM_005272656.4 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_005272713.1 | |
XM_005272659.4 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_005272716.1 | |
XM_011543957.2 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542259.1 | |
XM_011543958.2 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542260.1 | |
XM_011543959.2 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542261.1 | |
XM_011543960.2 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542262.1 | |
XM_011543961.2 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542263.1 | |
XM_011543962.2 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542264.1 | |
XM_011543963.2 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542265.1 | |
XM_011543964.2 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542266.1 | |
XM_011543965.2 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542267.1 | |
XM_011543966.2 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542268.1 | |
XM_011543967.2 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542269.1 | |
XM_011543968.2 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542270.1 | |
XM_011543969.2 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542271.1 | |
XM_011543970.2 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542272.1 | |
XM_011543971.2 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542273.1 | |
XM_011543972.2 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542274.1 | |
XM_011543973.2 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542275.1 | |
XM_011543974.1 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_011542276.1 | |
XM_011543975.2 | 465 | Intron | XP_011542277.1 | |||
XM_017029782.1 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_016885271.1 | |
XM_017029783.1 | 465 | Missense Mutation | ACG,GCG | T,A 30 | XP_016885272.1 | |
XM_017029784.1 | 465 | UTR 5 | XP_016885273.1 | |||
XM_017029785.1 | 465 | UTR 5 | XP_016885274.1 |