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TGAAGAGCAGAAAGAATTTCAAAAA[A/G]TGGCCTTTGACTTTGCTGCCCGAGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604773 MIM: 613739 MIM: 610027 | ||||||||||||||||||||
Literature Links: |
ACAD8 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 |
ACAD8 - acyl-CoA dehydrogenase family member 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014384.2 | 220 | Missense Mutation | ATG,GTG | M,V 51 | NP_055199.1 | |
XM_005271505.3 | 220 | Missense Mutation | ATG,GTG | M,V 51 | XP_005271562.1 | |
XM_011542750.2 | 220 | Missense Mutation | ATG,GTG | M,V 51 | XP_011541052.1 | |
XM_017017542.1 | 220 | Missense Mutation | ATG,GTG | M,V 51 | XP_016873031.1 | |
XM_017017543.1 | 220 | Missense Mutation | ATG,GTG | M,V 51 | XP_016873032.1 | |
XM_017017544.1 | 220 | Missense Mutation | ATG,GTG | M,V 51 | XP_016873033.1 | |
XM_017017545.1 | 220 | Missense Mutation | ATG,GTG | M,V 51 | XP_016873034.1 | |
XM_017017546.1 | 220 | Silent Mutation | AAA,AAG | K,K 9 | XP_016873035.1 | |
XM_017017547.1 | 220 | Silent Mutation | AAA,AAG | K,K 9 | XP_016873036.1 | |
XM_017017548.1 | 220 | Missense Mutation | ATG,GTG | M,V 51 | XP_016873037.1 | |
XM_017017549.1 | 220 | Missense Mutation | ATG,GTG | M,V 51 | XP_016873038.1 |
THYN1 - thymocyte nuclear protein 1 | ||||||
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There are no transcripts associated with this gene. |
VPS26B - VPS26, retromer complex component B | ||||||
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There are no transcripts associated with this gene. |