Product Details
- SNP ID
-
rs17852609
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:140659473 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CGTGCTCCTAGGGGAGGCTCAGTGT[C/G]GTCTCGTCTGCCCAAGCATTTTCAG
- Phenotype
-
MIM: 600758
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
PTK2
PubMed Links
Gene Details
- Gene
- PTK2
- Gene Name
- protein tyrosine kinase 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001199649.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1064R |
NP_001186578.1 |
NM_001316342.1 |
3258 |
Missense Mutation |
CCA,CGA |
P954R |
NP_001303271.1 |
NM_005607.4 |
3258 |
Missense Mutation |
CCA,CGA |
P1073R |
NP_005598.3 |
NM_153831.3 |
3258 |
Missense Mutation |
CCA,CGA |
P1051R |
NP_722560.1 |
XM_005251003.2 |
3258 |
Missense Mutation |
CCA,CGA |
P1139R |
XP_005251060.1 |
XM_005251012.2 |
3258 |
Missense Mutation |
CCA,CGA |
P1095R |
XP_005251069.1 |
XM_005251013.2 |
3258 |
Missense Mutation |
CCA,CGA |
P982R |
XP_005251070.1 |
XM_006716608.2 |
3258 |
Missense Mutation |
CCA,CGA |
P1095R |
XP_006716671.1 |
XM_006716609.2 |
3258 |
Missense Mutation |
CCA,CGA |
P982R |
XP_006716672.1 |
XM_006716610.2 |
3258 |
Missense Mutation |
CCA,CGA |
P982R |
XP_006716673.1 |
XM_011517194.2 |
3258 |
Missense Mutation |
CCA,CGA |
P1095R |
XP_011515496.1 |
XM_017013651.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1092R |
XP_016869140.1 |
XM_017013652.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1074R |
XP_016869141.1 |
XM_017013653.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1111R |
XP_016869142.1 |
XM_017013654.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1105R |
XP_016869143.1 |
XM_017013655.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1103R |
XP_016869144.1 |
XM_017013656.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1102R |
XP_016869145.1 |
XM_017013657.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1098R |
XP_016869146.1 |
XM_017013658.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1088R |
XP_016869147.1 |
XM_017013659.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1030R |
XP_016869148.1 |
XM_017013660.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1067R |
XP_016869149.1 |
XM_017013661.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1067R |
XP_016869150.1 |
XM_017013662.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1061R |
XP_016869151.1 |
XM_017013663.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1061R |
XP_016869152.1 |
XM_017013664.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1060R |
XP_016869153.1 |
XM_017013665.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1060R |
XP_016869154.1 |
XM_017013666.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1059R |
XP_016869155.1 |
XM_017013667.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1059R |
XP_016869156.1 |
XM_017013668.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1059R |
XP_016869157.1 |
XM_017013669.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1058R |
XP_016869158.1 |
XM_017013670.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1057R |
XP_016869159.1 |
XM_017013671.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1054R |
XP_016869160.1 |
XM_017013672.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1054R |
XP_016869161.1 |
XM_017013673.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1051R |
XP_016869162.1 |
XM_017013674.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1046R |
XP_016869163.1 |
XM_017013675.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1046R |
XP_016869164.1 |
XM_017013676.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1033R |
XP_016869165.1 |
XM_017013677.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1031R |
XP_016869166.1 |
XM_017013678.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1015R |
XP_016869167.1 |
XM_017013679.1 |
3258 |
Missense Mutation |
CCA,CGA |
P1010R |
XP_016869168.1 |
XM_017013680.1 |
3258 |
Missense Mutation |
CCA,CGA |
P994R |
XP_016869169.1 |
XM_017013681.1 |
3258 |
Missense Mutation |
CCA,CGA |
P979R |
XP_016869170.1 |
XM_017013682.1 |
3258 |
Missense Mutation |
CCA,CGA |
P975R |
XP_016869171.1 |
XM_017013683.1 |
3258 |
Missense Mutation |
CCA,CGA |
P954R |
XP_016869172.1 |
XM_017013684.1 |
3258 |
Missense Mutation |
CCA,CGA |
P948R |
XP_016869173.1 |
XM_017013685.1 |
3258 |
Missense Mutation |
CCA,CGA |
P947R |
XP_016869174.1 |
XM_017013686.1 |
3258 |
Missense Mutation |
CCA,CGA |
P941R |
XP_016869175.1 |
XM_017013687.1 |
3258 |
Missense Mutation |
CCA,CGA |
P933R |
XP_016869176.1 |
XM_017013688.1 |
3258 |
Missense Mutation |
CCA,CGA |
P918R |
XP_016869177.1 |
XM_017013689.1 |
3258 |
Missense Mutation |
CCA,CGA |
P918R |
XP_016869178.1 |
XM_017013690.1 |
3258 |
Missense Mutation |
CCA,CGA |
P912R |
XP_016869179.1 |
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