Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CATCCAGGCCAGTCAGTTGGAGGAG[C/T]TTTTTCCAGTGCAAAGACAGCTATG
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) - 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 |
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 | 1911 | Missense Mutation | GCT,GTT | A,V 617 | NP_055875.1 | |
XM_005249668.2 | 1911 | Missense Mutation | GCT,GTT | A,V 621 | XP_005249725.1 | |
XM_005249669.2 | 1911 | Missense Mutation | GCT,GTT | A,V 603 | XP_005249726.1 | |
XM_005249670.2 | 1911 | Missense Mutation | GCT,GTT | A,V 523 | XP_005249727.1 | |
XM_005249671.4 | 1911 | Intron | XP_005249728.1 | |||
XM_011515227.2 | 1911 | Missense Mutation | CTT,TTT | L,F 564 | XP_011513529.1 | |
XM_017011891.1 | 1911 | Missense Mutation | GCT,GTT | A,V 519 | XP_016867380.1 | |
XM_017011892.1 | 1911 | Missense Mutation | GCT,GTT | A,V 360 | XP_016867381.1 |
DPY19L1P1 - DPY19L1 pseudogene 1 | ||||||
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There are no transcripts associated with this gene. |