Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CATGGCTGCACTCACCCCAGCGGCC[C/T]GTGTGCTGCGCCCTGCTCCTCCATG
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 |
---|---|---|
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 |
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 | 1191 | Intron | NP_001123579.1 | |||
NM_005552.4 | 1191 | Intron | NP_005543.2 | |||
NM_182923.3 | 1191 | 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 | 1191 | Missense Mutation | AGG,GGG | R,G 271 | NP_001093588.1 | |
NM_001100119.1 | 1191 | Missense Mutation | AGG,GGG | R,G 271 | NP_001093589.1 | |
NM_005432.3 | 1191 | Missense Mutation | AGG,GGG | R,G 271 | NP_005423.1 | |
XM_005268046.2 | 1191 | Missense Mutation | AGG,GGG | R,G 271 | XP_005268103.1 | |
XM_011537138.2 | 1191 | Missense Mutation | AGG,GGG | R,G 271 | XP_011535440.1 |