Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGTGCTCCTAGGGGAGGCTCAGTGT[C/G]GTCTCGTCTGCCCAAGCATTTTCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600758 | ||||||||||||||||||||
Literature Links: |
PTK2 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 |
PTK2 - protein tyrosine kinase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199649.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1064 | NP_001186578.1 | |
NM_001316342.1 | 3258 | Missense Mutation | CCA,CGA | P,R 954 | NP_001303271.1 | |
NM_005607.4 | 3258 | Missense Mutation | CCA,CGA | P,R 1073 | NP_005598.3 | |
NM_153831.3 | 3258 | Missense Mutation | CCA,CGA | P,R 1051 | NP_722560.1 | |
XM_005251003.2 | 3258 | Missense Mutation | CCA,CGA | P,R 1139 | XP_005251060.1 | |
XM_005251012.2 | 3258 | Missense Mutation | CCA,CGA | P,R 1095 | XP_005251069.1 | |
XM_005251013.2 | 3258 | Missense Mutation | CCA,CGA | P,R 982 | XP_005251070.1 | |
XM_006716608.2 | 3258 | Missense Mutation | CCA,CGA | P,R 1095 | XP_006716671.1 | |
XM_006716609.2 | 3258 | Missense Mutation | CCA,CGA | P,R 982 | XP_006716672.1 | |
XM_006716610.2 | 3258 | Missense Mutation | CCA,CGA | P,R 982 | XP_006716673.1 | |
XM_011517194.2 | 3258 | Missense Mutation | CCA,CGA | P,R 1095 | XP_011515496.1 | |
XM_017013651.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1092 | XP_016869140.1 | |
XM_017013652.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1074 | XP_016869141.1 | |
XM_017013653.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1111 | XP_016869142.1 | |
XM_017013654.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1105 | XP_016869143.1 | |
XM_017013655.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1103 | XP_016869144.1 | |
XM_017013656.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1102 | XP_016869145.1 | |
XM_017013657.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1098 | XP_016869146.1 | |
XM_017013658.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1088 | XP_016869147.1 | |
XM_017013659.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1030 | XP_016869148.1 | |
XM_017013660.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1067 | XP_016869149.1 | |
XM_017013661.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1067 | XP_016869150.1 | |
XM_017013662.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1061 | XP_016869151.1 | |
XM_017013663.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1061 | XP_016869152.1 | |
XM_017013664.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1060 | XP_016869153.1 | |
XM_017013665.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1060 | XP_016869154.1 | |
XM_017013666.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1059 | XP_016869155.1 | |
XM_017013667.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1059 | XP_016869156.1 | |
XM_017013668.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1059 | XP_016869157.1 | |
XM_017013669.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1058 | XP_016869158.1 | |
XM_017013670.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1057 | XP_016869159.1 | |
XM_017013671.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1054 | XP_016869160.1 | |
XM_017013672.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1054 | XP_016869161.1 | |
XM_017013673.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1051 | XP_016869162.1 | |
XM_017013674.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1046 | XP_016869163.1 | |
XM_017013675.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1046 | XP_016869164.1 | |
XM_017013676.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1033 | XP_016869165.1 | |
XM_017013677.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1031 | XP_016869166.1 | |
XM_017013678.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1015 | XP_016869167.1 | |
XM_017013679.1 | 3258 | Missense Mutation | CCA,CGA | P,R 1010 | XP_016869168.1 | |
XM_017013680.1 | 3258 | Missense Mutation | CCA,CGA | P,R 994 | XP_016869169.1 | |
XM_017013681.1 | 3258 | Missense Mutation | CCA,CGA | P,R 979 | XP_016869170.1 | |
XM_017013682.1 | 3258 | Missense Mutation | CCA,CGA | P,R 975 | XP_016869171.1 | |
XM_017013683.1 | 3258 | Missense Mutation | CCA,CGA | P,R 954 | XP_016869172.1 | |
XM_017013684.1 | 3258 | Missense Mutation | CCA,CGA | P,R 948 | XP_016869173.1 | |
XM_017013685.1 | 3258 | Missense Mutation | CCA,CGA | P,R 947 | XP_016869174.1 | |
XM_017013686.1 | 3258 | Missense Mutation | CCA,CGA | P,R 941 | XP_016869175.1 | |
XM_017013687.1 | 3258 | Missense Mutation | CCA,CGA | P,R 933 | XP_016869176.1 | |
XM_017013688.1 | 3258 | Missense Mutation | CCA,CGA | P,R 918 | XP_016869177.1 | |
XM_017013689.1 | 3258 | Missense Mutation | CCA,CGA | P,R 918 | XP_016869178.1 | |
XM_017013690.1 | 3258 | Missense Mutation | CCA,CGA | P,R 912 | XP_016869179.1 |