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AGGCTCCTCGGGGCTCTGGGCCTCA[C/T]GCAGGAAGCGCTGGTAGCGCTCCAG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606994 | |||||||||||||||||||||||
Literature Links: |
LOC101929697 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 - 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 |
LOC101929697 - uncharacterized LOC101929697 | ||||||
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There are no transcripts associated with this gene. |
TNK2 - tyrosine kinase non receptor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001010938.1 | 3173 | Missense Mutation | CAT,CGT | H,R 955 | NP_001010938.1 | |
NM_001308046.1 | 3173 | Missense Mutation | CAT,CGT | H,R 909 | NP_001294975.1 | |
NM_005781.4 | 3173 | Missense Mutation | CAT,CGT | H,R 877 | NP_005772.3 | |
XM_005269268.3 | 3173 | Missense Mutation | CAT,CGT | H,R 955 | XP_005269325.1 | |
XM_005269270.3 | 3173 | Missense Mutation | CAT,CGT | H,R 892 | XP_005269327.1 | |
XM_005269274.3 | 3173 | Missense Mutation | CAT,CGT | H,R 653 | XP_005269331.1 | |
XM_005269275.3 | 3173 | Missense Mutation | CAT,CGT | H,R 578 | XP_005269332.1 | |
XM_011512317.2 | 3173 | Missense Mutation | CAT,CGT | H,R 1056 | XP_011510619.1 | |
XM_011512318.2 | 3173 | Missense Mutation | CAT,CGT | H,R 924 | XP_011510620.2 | |
XM_011512320.1 | 3173 | Missense Mutation | CAT,CGT | H,R 892 | XP_011510622.1 | |
XM_011512321.2 | 3173 | Missense Mutation | CAT,CGT | H,R 816 | XP_011510623.1 | |
XM_017005508.1 | 3173 | Missense Mutation | CAT,CGT | H,R 909 | XP_016860997.1 | |
XM_017005509.1 | 3173 | Missense Mutation | CAT,CGT | H,R 909 | XP_016860998.1 | |
XM_017005510.1 | 3173 | Missense Mutation | CAT,CGT | H,R 924 | XP_016860999.1 |