Product Details

SNP ID
rs150692762
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:81312551 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTTCTATTCCTTTACAGAGCGAAT[C/G]GTCACAGTTGGTCGCTGGGCAAAGG
Phenotype
MIM: 614315
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
ACOT12 PubMed Links

Gene Details

Gene
ACOT12
Gene Name
acyl-CoA thioesterase 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_130767.2 1195 Intron NP_570123.1
XM_006714531.2 1195 Intron XP_006714594.1
XM_006714532.3 1195 Intron XP_006714595.1
XM_017009045.1 1195 Intron XP_016864534.1
XM_017009046.1 1195 Intron XP_016864535.1
XM_017009047.1 1195 Intron XP_016864536.1
XM_017009048.1 1195 Intron XP_016864537.1
Gene
ZCCHC9
Gene Name
zinc finger CCHC-type containing 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001131035.1 1195 Missense Mutation ATC,ATG I235M NP_001124507.1
NM_001131036.1 1195 Missense Mutation ATC,ATG I235M NP_001124508.1
NM_032280.2 1195 Missense Mutation ATC,ATG I235M NP_115656.1
XM_005248616.3 1195 Missense Mutation ATC,ATG I84M XP_005248673.1

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