Product Details

SNP ID
rs188624641
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:99828152 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCAAACTTTGCCATGGAAACATGG[A/G]TTCTTGTGGCTACCAGCCTGGTACT
Phenotype
MIM: 606534
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CYP3A43 PubMed Links

Gene Details

Gene
CYP3A43
Gene Name
cytochrome P450 family 3 subfamily A member 43
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001278921.1 140 Missense Mutation ATT,GTT I13V NP_001265850.1
NM_022820.4 140 Missense Mutation ATT,GTT I13V NP_073731.1
NM_057095.2 140 Missense Mutation ATT,GTT I13V NP_476436.1
NM_057096.3 140 Missense Mutation ATT,GTT I13V NP_476437.1
XM_017012542.1 140 Intron XP_016868031.1
XM_017012543.1 140 Intron XP_016868032.1
XM_017012544.1 140 Intron XP_016868033.1
XM_017012545.1 140 Intron XP_016868034.1

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