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TGTTTTACATCACATTTTTTGATTT[C/G]TTATGAGGCTGGACACTTTTTTATA
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 | |||
---|---|---|---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba)
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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 |
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 | Intron | NP_055875.1 | ||||
XM_005249668.2 | Intron | XP_005249725.1 | ||||
XM_005249669.2 | Intron | XP_005249726.1 | ||||
XM_005249670.2 | Intron | XP_005249727.1 | ||||
XM_005249671.4 | Intron | XP_005249728.1 | ||||
XM_011515227.2 | Intron | XP_011513529.1 | ||||
XM_017011891.1 | Intron | XP_016867380.1 | ||||
XM_017011892.1 | Intron | XP_016867381.1 |