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TGAGGGTCTTGCTGTCACCACTAAG[C/T]GAATCCTGCAGCAGGTAGGTGAGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 602703 MIM: 604535 | ||||||||||||||||||||
Literature Links: |
KATNB1 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 |
KATNB1 - katanin regulatory subunit B1 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
KIFC3 - kinesin family member C3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130099.1 | 2949 | Silent Mutation | TCA,TCG | S,S 593 | NP_001123571.1 | |
NM_001130100.1 | 2949 | Silent Mutation | TCA,TCG | S,S 732 | NP_001123572.1 | |
NM_001318710.1 | 2949 | Silent Mutation | TCA,TCG | S,S 754 | NP_001305639.1 | |
NM_001318711.1 | 2949 | Silent Mutation | TCA,TCG | S,S 674 | NP_001305640.1 | |
NM_001318712.1 | 2949 | Silent Mutation | TCA,TCG | S,S 630 | NP_001305641.1 | |
NM_001318713.1 | 2949 | Silent Mutation | TCA,TCG | S,S 590 | NP_001305642.1 | |
NM_001318714.1 | 2949 | Silent Mutation | TCA,TCG | S,S 593 | NP_001305643.1 | |
NM_001318715.1 | 2949 | Silent Mutation | TCA,TCG | S,S 593 | NP_001305644.1 | |
NM_005550.3 | 2949 | Silent Mutation | TCA,TCG | S,S 732 | NP_005541.3 | |
XM_005255937.1 | 2949 | Silent Mutation | TCA,TCG | S,S 895 | XP_005255994.1 | |
XM_005255944.1 | 2949 | Silent Mutation | TCA,TCG | S,S 674 | XP_005256001.1 | |
XM_006721188.1 | 2949 | Silent Mutation | TCA,TCG | S,S 921 | XP_006721251.1 | |
XM_011523075.1 | 2949 | Silent Mutation | TCA,TCG | S,S 781 | XP_011521377.1 | |
XM_011523076.1 | 2949 | Silent Mutation | TCA,TCG | S,S 781 | XP_011521378.1 | |
XM_011523077.1 | 2949 | Silent Mutation | TCA,TCG | S,S 760 | XP_011521379.1 | |
XM_011523078.1 | 2949 | Silent Mutation | TCA,TCG | S,S 593 | XP_011521380.1 | |
XM_011523079.1 | 2949 | Silent Mutation | TCA,TCG | S,S 593 | XP_011521381.1 | |
XM_017023219.1 | 2949 | Silent Mutation | TCA,TCG | S,S 978 | XP_016878708.1 | |
XM_017023220.1 | 2949 | Silent Mutation | TCA,TCG | S,S 956 | XP_016878709.1 | |
XM_017023221.1 | 2949 | Silent Mutation | TCA,TCG | S,S 895 | XP_016878710.1 | |
XM_017023222.1 | 2949 | Silent Mutation | TCA,TCG | S,S 811 | XP_016878711.1 | |
XM_017023223.1 | 2949 | Silent Mutation | TCA,TCG | S,S 754 | XP_016878712.1 | |
XM_017023224.1 | 2949 | Silent Mutation | TCA,TCG | S,S 811 | XP_016878713.1 | |
XM_017023225.1 | 2949 | Silent Mutation | TCA,TCG | S,S 675 | XP_016878714.1 | |
XM_017023226.1 | 2949 | Silent Mutation | TCA,TCG | S,S 674 | XP_016878715.1 | |
XM_017023227.1 | 2949 | Silent Mutation | TCA,TCG | S,S 674 | XP_016878716.1 |