Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCAAATGATTCAAAATAAGGCAGC[A/G]ATTGATAGATGGCAAATGCTGTTAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615941 | ||||||||||||||||||||
Literature Links: |
HACD4 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 |
HACD4 - 3-hydroxyacyl-CoA dehydratase 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001010915.4 | 937 | Missense Mutation | TCG,TTG | S,L 170 | NP_001010915.2 | |
NM_001321883.1 | 937 | Missense Mutation | TCG,TTG | S,L 133 | NP_001308812.1 | |
NM_001321903.1 | 937 | Missense Mutation | TCG,TTG | S,L 221 | NP_001308832.1 | |
XM_011517876.2 | 937 | Missense Mutation | TCG,TTG | S,L 96 | XP_011516178.1 | |
XM_017014713.1 | 937 | Missense Mutation | TCG,TTG | S,L 184 | XP_016870202.1 | |
XM_017014714.1 | 937 | Missense Mutation | CGC,TGC | R,C 202 | XP_016870203.1 |