Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCCTCTCTCGGAGTTGGCAGGAAG[C/T]CAGGTTGCAGGGTGTCCGCTTCCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 610465 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ACSF2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
ACSF2 - acyl-CoA synthetase family member 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001288968.1 | 205 | Missense Mutation | GCC,GTC | A,V 34 | NP_001275897.1 | |
NM_001288969.1 | 205 | Missense Mutation | GCC,GTC | A,V 34 | NP_001275898.1 | |
NM_001288970.1 | 205 | Missense Mutation | GCC,GTC | A,V 34 | NP_001275899.1 | |
NM_001288971.1 | 205 | UTR 5 | NP_001275900.1 | |||
NM_001288972.1 | 205 | UTR 5 | NP_001275901.1 | |||
NM_025149.5 | 205 | Missense Mutation | GCC,GTC | A,V 34 | NP_079425.3 | |
XM_006722110.3 | 205 | Missense Mutation | GCC,GTC | A,V 34 | XP_006722173.1 | |
XM_011525294.1 | 205 | Missense Mutation | GCC,GTC | A,V 34 | XP_011523596.1 |