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GCTGAGACCCCCCAGGTTAGATCCC[C/T]GGAAGCAGAGCCAGAAAGCAGAAAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612034 MIM: 600487 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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)
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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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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 | 2129 | Intron | NP_005874.1 | |||
XM_005259475.2 | 2129 | Intron | XP_005259532.1 | |||
XM_006722607.2 | 2129 | Intron | XP_006722670.1 | |||
XM_006722608.3 | 2129 | Intron | XP_006722671.2 | |||
XM_006722609.3 | 2129 | Intron | XP_006722672.1 | |||
XM_006722610.3 | 2129 | Intron | XP_006722673.2 |
C19orf25 - chromosome 19 open reading frame 25 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152482.2 | 2129 | UTR 3 | NP_689695.2 | |||
XM_005259506.3 | 2129 | UTR 3 | XP_005259563.1 | |||
XM_006722653.3 | 2129 | UTR 3 | XP_006722716.1 | |||
XM_017026374.1 | 2129 | UTR 3 | XP_016881863.1 |
PCSK4 - proprotein convertase subtilisin/kexin type 4 | ||||||
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There are no transcripts associated with this gene. |