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TTCTCCAGGCCCCCATCAGAAGACG[A/G]AAAGCAGCACTCACCCCAGCTATCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602572 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ANXA11 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
|
ANXA11 - annexin A11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001157.2 | Intron | NP_001148.1 | ||||
NM_001278407.1 | Intron | NP_001265336.1 | ||||
NM_001278408.1 | Intron | NP_001265337.1 | ||||
NM_001278409.1 | Intron | NP_001265338.1 | ||||
NM_145868.1 | Intron | NP_665875.1 | ||||
NM_145869.1 | Intron | NP_665876.1 | ||||
XM_005269741.4 | Intron | XP_005269798.1 | ||||
XM_005269742.1 | Intron | XP_005269799.1 | ||||
XM_006717813.1 | Intron | XP_006717876.1 | ||||
XM_006717814.3 | Intron | XP_006717877.1 | ||||
XM_011539735.1 | Intron | XP_011538037.1 | ||||
XM_011539736.2 | Intron | XP_011538038.1 |