Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGGATACTCTCATCTGCGTCAGGA[C/G]CCAGGTTGTACACAAATATACACCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601673 | ||||||||||||||||||||
Literature Links: |
ELAVL2 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 |
ELAVL2 - ELAV like neuron-specific RNA binding protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001171195.1 | 1366 | Missense Mutation | GCT,GGT | A,G 271 | NP_001164666.1 | |
NM_001171197.1 | 1366 | Missense Mutation | GCT,GGT | A,G 271 | NP_001164668.1 | |
NM_004432.3 | 1366 | Missense Mutation | GCT,GGT | A,G 284 | NP_004423.2 | |
XM_005251393.3 | 1366 | Missense Mutation | GCT,GGT | A,G 285 | XP_005251450.1 | |
XM_005251394.3 | 1366 | Missense Mutation | GCT,GGT | A,G 285 | XP_005251451.1 | |
XM_005251395.3 | 1366 | Missense Mutation | GCT,GGT | A,G 285 | XP_005251452.1 | |
XM_006716734.3 | 1366 | Missense Mutation | GCT,GGT | A,G 314 | XP_006716797.1 | |
XM_006716735.3 | 1366 | Missense Mutation | GCT,GGT | A,G 314 | XP_006716798.1 | |
XM_006716736.3 | 1366 | Missense Mutation | GCT,GGT | A,G 285 | XP_006716799.1 | |
XM_011517774.2 | 1366 | Missense Mutation | GCT,GGT | A,G 313 | XP_011516076.1 | |
XM_011517776.2 | 1366 | Missense Mutation | GCT,GGT | A,G 301 | XP_011516078.1 | |
XM_011517777.2 | 1366 | Missense Mutation | GCT,GGT | A,G 300 | XP_011516079.1 | |
XM_011517778.2 | 1366 | Missense Mutation | GCT,GGT | A,G 317 | XP_011516080.2 | |
XM_011517779.2 | 1366 | Missense Mutation | GCT,GGT | A,G 314 | XP_011516081.1 | |
XM_011517780.2 | 1366 | Missense Mutation | GCT,GGT | A,G 314 | XP_011516082.1 | |
XM_011517783.2 | 1366 | Missense Mutation | GCT,GGT | A,G 299 | XP_011516085.1 | |
XM_011517784.2 | 1366 | Missense Mutation | GCT,GGT | A,G 285 | XP_011516086.1 | |
XM_011517785.2 | 1366 | Missense Mutation | GCT,GGT | A,G 285 | XP_011516087.1 | |
XM_011517786.2 | 1366 | Missense Mutation | GCT,GGT | A,G 285 | XP_011516088.1 | |
XM_017014408.1 | 1366 | Missense Mutation | GCT,GGT | A,G 313 | XP_016869897.1 | |
XM_017014409.1 | 1366 | Missense Mutation | GCT,GGT | A,G 313 | XP_016869898.1 | |
XM_017014410.1 | 1366 | Missense Mutation | GCT,GGT | A,G 313 | XP_016869899.1 | |
XM_017014411.1 | 1366 | Missense Mutation | GCT,GGT | A,G 313 | XP_016869900.1 | |
XM_017014412.1 | 1366 | Missense Mutation | GCT,GGT | A,G 313 | XP_016869901.1 | |
XM_017014413.1 | 1366 | Missense Mutation | GCT,GGT | A,G 312 | XP_016869902.1 | |
XM_017014414.1 | 1366 | Missense Mutation | GCT,GGT | A,G 312 | XP_016869903.1 | |
XM_017014415.1 | 1366 | Missense Mutation | GCT,GGT | A,G 301 | XP_016869904.1 | |
XM_017014416.1 | 1366 | Missense Mutation | GCT,GGT | A,G 300 | XP_016869905.1 | |
XM_017014417.1 | 1366 | Missense Mutation | GCT,GGT | A,G 298 | XP_016869906.1 | |
XM_017014418.1 | 1366 | Missense Mutation | GCT,GGT | A,G 285 | XP_016869907.1 | |
XM_017014419.1 | 1366 | Missense Mutation | GCT,GGT | A,G 284 | XP_016869908.1 | |
XM_017014420.1 | 1366 | Missense Mutation | GCT,GGT | A,G 284 | XP_016869909.1 | |
XM_017014421.1 | 1366 | Missense Mutation | GCT,GGT | A,G 284 | XP_016869910.1 | |
XM_017014422.1 | 1366 | Missense Mutation | GCT,GGT | A,G 284 | XP_016869911.1 | |
XM_017014423.1 | 1366 | Missense Mutation | GCT,GGT | A,G 284 | XP_016869912.1 | |
XM_017014424.1 | 1366 | Missense Mutation | GCT,GGT | A,G 271 | XP_016869913.1 | |
XM_017014425.1 | 1366 | Missense Mutation | GCT,GGT | A,G 271 | XP_016869914.1 | |
XM_017014426.1 | 1366 | Missense Mutation | GCT,GGT | A,G 150 | XP_016869915.1 |