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CATGGCTTTCCACTTTCACCACTTC[C/G]ACCTCCCAAAGTCTCACTGAGCCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612927 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
AVL9 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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AVL9 - AVL9 cell migration associated | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015060.2 | 1966 | Silent Mutation | TCC,TCG | S,S 635 | NP_055875.1 | |
XM_005249668.2 | 1966 | Silent Mutation | TCC,TCG | S,S 639 | XP_005249725.1 | |
XM_005249669.2 | 1966 | Silent Mutation | TCC,TCG | S,S 621 | XP_005249726.1 | |
XM_005249670.2 | 1966 | Silent Mutation | TCC,TCG | S,S 541 | XP_005249727.1 | |
XM_005249671.4 | 1966 | Intron | XP_005249728.1 | |||
XM_011515227.2 | 1966 | Missense Mutation | CCA,CGA | P,R 582 | XP_011513529.1 | |
XM_017011891.1 | 1966 | Silent Mutation | TCC,TCG | S,S 537 | XP_016867380.1 | |
XM_017011892.1 | 1966 | Silent Mutation | TCC,TCG | S,S 378 | XP_016867381.1 |
DPY19L1P1 - DPY19L1 pseudogene 1 | ||||||
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There are no transcripts associated with this gene. |