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- SNP ID:
- rs150356089
- Gene
-
PXNPXN-AS1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.12: 120212377 - 120212377 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
GCTTGTCGTTCTGCTCCTTGAAGGT[A/G]CCCTTGTTGAGCTGCTTGAGGCAGA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 602505
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Literature Links: |
PXN PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| PXN - paxillin | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001080855.2 | 2536 | Silent Mutation | GGC,GGT | G,G 571 | NP_001074324.1 | |
| NM_001243756.1 | 2536 | Silent Mutation | GGC,GGT | G,G 585 | NP_001230685.1 | |
| NM_002859.3 | 2536 | Silent Mutation | GGC,GGT | G,G 537 | NP_002850.2 | |
| NM_025157.4 | 2536 | Silent Mutation | GGC,GGT | G,G 404 | NP_079433.3 | |
| XM_005253917.3 | 2536 | Silent Mutation | GGC,GGT | G,G 383 | XP_005253974.1 | |
| XM_006719532.1 | 2536 | Silent Mutation | GGC,GGT | G,G 1109 | XP_006719595.1 | |
| XM_006719534.1 | 2536 | Silent Mutation | GGC,GGT | G,G 976 | XP_006719597.1 | |
| XM_006719535.3 | 2536 | Silent Mutation | GGC,GGT | G,G 976 | XP_006719598.1 | |
| XM_006719536.2 | 2536 | Silent Mutation | GGC,GGT | G,G 976 | XP_006719599.1 | |
| XM_011538622.1 | 2536 | Silent Mutation | GGC,GGT | G,G 976 | XP_011536924.1 | |
| XM_011538623.1 | 2536 | Silent Mutation | GGC,GGT | G,G 976 | XP_011536925.1 | |
| XM_017019726.1 | 2536 | Silent Mutation | GGC,GGT | G,G 1115 | XP_016875215.1 | |
| XM_017019727.1 | 2536 | Silent Mutation | GGC,GGT | G,G 1110 | XP_016875216.1 | |
| XM_017019728.1 | 2536 | Silent Mutation | GGC,GGT | G,G 1107 | XP_016875217.1 | |
| XM_017019729.1 | 2536 | Silent Mutation | GGC,GGT | G,G 1067 | XP_016875218.1 | |
| XM_017019730.1 | 2536 | Intron | XP_016875219.1 | |||
| XM_017019731.1 | 2536 | Silent Mutation | GGC,GGT | G,G 976 | XP_016875220.1 | |
| XM_017019732.1 | 2536 | Intron | XP_016875221.1 | |||
| XM_017019733.1 | 2536 | Silent Mutation | GGC,GGT | G,G 920 | XP_016875222.1 | |
| XM_017019734.1 | 2536 | Silent Mutation | GGC,GGT | G,G 868 | XP_016875223.1 | |
| XM_017019735.1 | 2536 | Silent Mutation | GGC,GGT | G,G 838 | XP_016875224.1 | |
| XM_017019736.1 | 2536 | Silent Mutation | GGC,GGT | G,G 728 | XP_016875225.1 | |
| XM_017019737.1 | 2536 | Silent Mutation | GGC,GGT | G,G 680 | XP_016875226.1 | |
| XM_017019738.1 | 2536 | Silent Mutation | GGC,GGT | G,G 625 | XP_016875227.1 | |
| XM_017019739.1 | 2536 | Silent Mutation | GGC,GGT | G,G 591 | XP_016875228.1 | |
| XM_017019740.1 | 2536 | Silent Mutation | GGC,GGT | G,G 577 | XP_016875229.1 | |
| XM_017019741.1 | 2536 | Silent Mutation | GGC,GGT | G,G 569 | XP_016875230.1 | |
| XM_017019742.1 | 2536 | Silent Mutation | GGC,GGT | G,G 543 | XP_016875231.1 | |
| XM_017019743.1 | 2536 | Silent Mutation | GGC,GGT | G,G 404 | XP_016875232.1 | |
| PXN-AS1 - PXN antisense RNA 1 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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