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AAGCCAGCGCGCTGGCAGAGTCAAG[A/G]GATGGGGCAGGGGCTGCCGGGGCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612034 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
APC2 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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APC2 - APC2, WNT signaling pathway regulator | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005883.2 | 75 | Intron | NP_005874.1 | |||
XM_005259475.2 | 75 | Intron | XP_005259532.1 | |||
XM_006722607.2 | 75 | Intron | XP_006722670.1 | |||
XM_006722608.3 | 75 | Intron | XP_006722671.2 | |||
XM_006722609.3 | 75 | UTR 5 | XP_006722672.1 | |||
XM_006722610.3 | 75 | Intron | XP_006722673.2 |