Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGTTAATCAGCTCAAAGATTTGTTG[C/T]GCCAACAAGCAGATAAGGAAAGTGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
6 submissions
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Phenotype: |
MIM: 613524 | ||||||||||||||||||||
Literature Links: |
SDCCAG8 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 |
SDCCAG8 - serologically defined colon cancer antigen 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006642.3 | 381 | Missense Mutation | CGC,TGC | R,C 82 | NP_006633.1 | |
XM_005273013.4 | 381 | Missense Mutation | CGC,TGC | R,C 82 | XP_005273070.1 | |
XM_005273018.1 | 381 | UTR 5 | XP_005273075.1 | |||
XM_005273021.4 | 381 | UTR 5 | XP_005273078.1 | |||
XM_005273022.3 | 381 | UTR 5 | XP_005273079.1 | |||
XM_005273023.4 | 381 | Missense Mutation | CGC,TGC | R,C 82 | XP_005273080.1 | |
XM_006711727.3 | 381 | Missense Mutation | CGC,TGC | R,C 92 | XP_006711790.1 | |
XM_006711728.3 | 381 | Missense Mutation | CGC,TGC | R,C 92 | XP_006711791.1 | |
XM_011544021.2 | 381 | Missense Mutation | CGC,TGC | R,C 92 | XP_011542323.1 | |
XM_011544022.2 | 381 | Missense Mutation | CGC,TGC | R,C 82 | XP_011542324.1 | |
XM_011544023.2 | 381 | Missense Mutation | CGC,TGC | R,C 92 | XP_011542325.1 | |
XM_011544024.2 | 381 | Missense Mutation | CGC,TGC | R,C 92 | XP_011542326.1 | |
XM_011544026.2 | 381 | Missense Mutation | CGC,TGC | R,C 92 | XP_011542328.1 | |
XM_011544028.2 | 381 | Missense Mutation | CGC,TGC | R,C 92 | XP_011542330.1 | |
XM_011544029.2 | 381 | Missense Mutation | CGC,TGC | R,C 92 | XP_011542331.1 | |
XM_011544030.2 | 381 | Intron | XP_011542332.1 | |||
XM_017000103.1 | 381 | Missense Mutation | CGC,TGC | R,C 92 | XP_016855592.1 | |
XM_017000104.1 | 381 | Missense Mutation | CGC,TGC | R,C 82 | XP_016855593.1 | |
XM_017000105.1 | 381 | Missense Mutation | CGC,TGC | R,C 82 | XP_016855594.1 | |
XM_017000106.1 | 381 | UTR 5 | XP_016855595.1 | |||
XM_017000107.1 | 381 | UTR 5 | XP_016855596.1 | |||
XM_017000108.1 | 381 | UTR 5 | XP_016855597.1 | |||
XM_017000109.1 | 381 | Missense Mutation | CGC,TGC | R,C 92 | XP_016855598.1 |