Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCAAGCTGGAGACAGAGACGTCGG[C/G]CATGAAGGTGGGGGCCTACATGGAG
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 | 486 | Missense Mutation | GCC,GGC | A,G 45 | NP_005874.1 | |
XM_005259475.2 | 486 | Missense Mutation | GCC,GGC | A,G 69 | XP_005259532.1 | |
XM_006722607.2 | 486 | Missense Mutation | GCC,GGC | A,G 69 | XP_006722670.1 | |
XM_006722608.3 | 486 | Missense Mutation | GCC,GGC | A,G 146 | XP_006722671.2 | |
XM_006722609.3 | 486 | Missense Mutation | GCC,GGC | A,G 45 | XP_006722672.1 | |
XM_006722610.3 | 486 | Missense Mutation | GCC,GGC | A,G 146 | XP_006722673.2 |