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GCGAACATGTCGAAGTAGTCCTTGC[A/G]ACAGTAGGCCTTGCCGTCCTTCTCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602505 | ||||||||||||||||||||
Literature Links: |
PXN 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 |
PXN - paxillin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080855.2 | 2216 | Missense Mutation | CGC,TGC | R,C 465 | NP_001074324.1 | |
NM_001243756.1 | 2216 | Missense Mutation | CGC,TGC | R,C 479 | NP_001230685.1 | |
NM_002859.3 | 2216 | Missense Mutation | CGC,TGC | R,C 431 | NP_002850.2 | |
NM_025157.4 | 2216 | Missense Mutation | CGC,TGC | R,C 298 | NP_079433.3 | |
XM_005253917.3 | 2216 | Missense Mutation | CGC,TGC | R,C 277 | XP_005253974.1 | |
XM_006719532.1 | 2216 | Missense Mutation | CGC,TGC | R,C 1003 | XP_006719595.1 | |
XM_006719534.1 | 2216 | Missense Mutation | CGC,TGC | R,C 870 | XP_006719597.1 | |
XM_006719535.3 | 2216 | Missense Mutation | CGC,TGC | R,C 870 | XP_006719598.1 | |
XM_006719536.2 | 2216 | Missense Mutation | CGC,TGC | R,C 870 | XP_006719599.1 | |
XM_011538622.1 | 2216 | Missense Mutation | CGC,TGC | R,C 870 | XP_011536924.1 | |
XM_011538623.1 | 2216 | Missense Mutation | CGC,TGC | R,C 870 | XP_011536925.1 | |
XM_017019726.1 | 2216 | Missense Mutation | CGC,TGC | R,C 1009 | XP_016875215.1 | |
XM_017019727.1 | 2216 | Missense Mutation | CGC,TGC | R,C 1004 | XP_016875216.1 | |
XM_017019728.1 | 2216 | Missense Mutation | CGC,TGC | R,C 1001 | XP_016875217.1 | |
XM_017019729.1 | 2216 | Missense Mutation | CGC,TGC | R,C 961 | XP_016875218.1 | |
XM_017019730.1 | 2216 | Missense Mutation | CGC,TGC | R,C 1009 | XP_016875219.1 | |
XM_017019731.1 | 2216 | Missense Mutation | CGC,TGC | R,C 870 | XP_016875220.1 | |
XM_017019732.1 | 2216 | Intron | XP_016875221.1 | |||
XM_017019733.1 | 2216 | Missense Mutation | CGC,TGC | R,C 814 | XP_016875222.1 | |
XM_017019734.1 | 2216 | Missense Mutation | CGC,TGC | R,C 762 | XP_016875223.1 | |
XM_017019735.1 | 2216 | Missense Mutation | CGC,TGC | R,C 732 | XP_016875224.1 | |
XM_017019736.1 | 2216 | Missense Mutation | CGC,TGC | R,C 622 | XP_016875225.1 | |
XM_017019737.1 | 2216 | Missense Mutation | CGC,TGC | R,C 574 | XP_016875226.1 | |
XM_017019738.1 | 2216 | Missense Mutation | CGC,TGC | R,C 519 | XP_016875227.1 | |
XM_017019739.1 | 2216 | Missense Mutation | CGC,TGC | R,C 485 | XP_016875228.1 | |
XM_017019740.1 | 2216 | Missense Mutation | CGC,TGC | R,C 471 | XP_016875229.1 | |
XM_017019741.1 | 2216 | Missense Mutation | CGC,TGC | R,C 463 | XP_016875230.1 | |
XM_017019742.1 | 2216 | Missense Mutation | CGC,TGC | R,C 437 | XP_016875231.1 | |
XM_017019743.1 | 2216 | Missense Mutation | CGC,TGC | R,C 298 | XP_016875232.1 |
PXN-AS1 - PXN antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |