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CCAGGGTCACCTTGAGTTCATGGCA[A/G]GTTGTATATGCCAAGCACCCCATCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602572 MIM: 612857 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ANXA11 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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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 |
PLAC9 - placenta specific 9 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |