Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGATCTTCCCAAAAGACGTGAGAAG[C/T]ATCAGAGAATTGCAAATGCAAGGTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 200350 | ||||||||||||||||||||
Literature Links: |
ACACA 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 |
ACACA - acetyl-CoA carboxylase alpha | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_198834.2 | 504 | Intron | NP_942131.1 | |||
NM_198836.2 | 504 | Intron | NP_942133.1 | |||
NM_198837.1 | 504 | Intron | NP_942134.1 | |||
NM_198838.1 | 504 | Intron | NP_942135.1 | |||
NM_198839.2 | 504 | Intron | NP_942136.1 | |||
XM_005257267.4 | 504 | Intron | XP_005257324.1 | |||
XM_006721853.1 | 504 | Intron | XP_006721916.1 | |||
XM_011524701.1 | 504 | Intron | XP_011523003.1 | |||
XM_011524703.1 | 504 | Intron | XP_011523005.1 | |||
XM_011524704.2 | 504 | Intron | XP_011523006.1 | |||
XM_017024553.1 | 504 | Intron | XP_016880042.1 | |||
XM_017024554.1 | 504 | Intron | XP_016880043.1 | |||
XM_017024555.1 | 504 | Intron | XP_016880044.1 |
C17orf78 - chromosome 17 open reading frame 78 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321399.1 | 504 | Silent Mutation | AGC,AGT | S,S 41 | NP_001308328.1 | |
NM_173625.4 | 504 | Silent Mutation | AGC,AGT | S,S 41 | NP_775896.3 | |
XM_011524647.2 | 504 | Intron | XP_011522949.1 | |||
XM_011524648.2 | 504 | Silent Mutation | AGC,AGT | S,S 41 | XP_011522950.1 | |
XM_011524649.2 | 504 | Silent Mutation | AGC,AGT | S,S 41 | XP_011522951.1 |