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ACATGCCGCAGAGGACGGGGCCTCC[A/G]AGGGTCACGGCCAGGAGGCTCAGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612034 MIM: 600487 MIM: 609346 | ||||||||||||||||||||
Literature Links: |
APC2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
APC2 - APC2, WNT signaling pathway regulator | ||||||
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There are no transcripts associated with this gene. |
C19orf25 - chromosome 19 open reading frame 25 | ||||||
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There are no transcripts associated with this gene. |
PCSK4 - proprotein convertase subtilisin/kexin type 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017573.4 | 1821 | Silent Mutation | CTC,CTT | L,L 719 | NP_060043.2 | |
XM_005259586.1 | 1821 | Silent Mutation | CTC,CTT | L,L 531 | XP_005259643.1 | |
XM_011528085.2 | 1821 | Silent Mutation | CTC,CTT | L,L 746 | XP_011526387.1 | |
XM_011528086.2 | 1821 | Silent Mutation | CTC,CTT | L,L 737 | XP_011526388.1 | |
XM_011528087.2 | 1821 | Silent Mutation | CTC,CTT | L,L 688 | XP_011526389.1 | |
XM_011528088.2 | 1821 | Silent Mutation | CTC,CTT | L,L 684 | XP_011526390.1 | |
XM_011528089.2 | 1821 | Silent Mutation | CTC,CTT | L,L 652 | XP_011526391.1 | |
XM_011528090.2 | 1821 | Silent Mutation | CTC,CTT | L,L 625 | XP_011526392.1 | |
XM_011528091.2 | 1821 | Silent Mutation | CTC,CTT | L,L 622 | XP_011526393.1 | |
XM_011528092.2 | 1821 | Intron | XP_011526394.1 | |||
XM_011528093.2 | 1821 | UTR 3 | XP_011526395.1 | |||
XM_011528094.1 | 1821 | Silent Mutation | CTC,CTT | L,L 531 | XP_011526396.1 | |
XM_011528095.2 | 1821 | Intron | XP_011526397.1 | |||
XM_011528096.1 | 1821 | Silent Mutation | CTC,CTT | L,L 497 | XP_011526398.1 | |
XM_017026897.1 | 1821 | Intron | XP_016882386.1 |
REEP6 - receptor accessory protein 6 | ||||||
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There are no transcripts associated with this gene. |