Product Details

SNP ID
rs142741321
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:139737987 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCAGGGAACAGGCTGATAAATATTA[G/T]AAGAATTATAGCCAACCATGTGGAT
Phenotype
MIM: 300516
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
ATP11C PubMed Links

Gene Details

Gene
ATP11C
Gene Name
ATPase phospholipid transporting 11C
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001010986.2 3942 Silent Mutation NP_001010986.1
NM_173694.4 3942 Silent Mutation NP_775965.2
XM_017029439.1 3942 Silent Mutation XP_016884928.1
XM_017029440.1 3942 Silent Mutation XP_016884929.1
XM_017029441.1 3942 Silent Mutation XP_016884930.1
XM_017029442.1 3942 Silent Mutation XP_016884931.1
XM_017029443.1 3942 Silent Mutation XP_016884932.1
XM_017029444.1 3942 Silent Mutation XP_016884933.1
XM_017029445.1 3942 Silent Mutation XP_016884934.1
XM_017029446.1 3942 Silent Mutation XP_016884935.1
XM_017029447.1 3942 Silent Mutation XP_016884936.1
XM_017029448.1 3942 Missense Mutation XP_016884937.1
XM_017029449.1 3942 Silent Mutation XP_016884938.1

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