Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600025 MIM: 600675 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
KLC1 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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KLC1 - kinesin light chain 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130107.1 | 1102 | Intron | NP_001123579.1 | |||
NM_005552.4 | 1102 | Intron | NP_005543.2 | |||
NM_182923.3 | 1102 | Intron | NP_891553.2 |
XRCC3 - X-ray repair cross complementing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001100118.1 | 1102 | Missense Mutation | ACG,ATG | T,M 241 | NP_001093588.1 | |
NM_001100119.1 | 1102 | Missense Mutation | ACG,ATG | T,M 241 | NP_001093589.1 | |
NM_005432.3 | 1102 | Missense Mutation | ACG,ATG | T,M 241 | NP_005423.1 | |
XM_005268046.2 | 1102 | Missense Mutation | ACG,ATG | T,M 241 | XP_005268103.1 | |
XM_011537138.2 | 1102 | Missense Mutation | ACG,ATG | T,M 241 | XP_011535440.1 |
Set Membership: |
HapMap |