Product Details

SNP ID
rs145066502
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:139738794 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTGTCTGAGCTGAACCACAGAGAG[C/T]CTCAGTAGGTGAAGCTATTGTTCTT
Phenotype
MIM: 300516
Polymorphism
C/T, Transition 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 Intron NP_001010986.1
NM_173694.4 Intron NP_775965.2
XM_017029439.1 Intron XP_016884928.1
XM_017029440.1 Intron XP_016884929.1
XM_017029441.1 Intron XP_016884930.1
XM_017029442.1 Intron XP_016884931.1
XM_017029443.1 Intron XP_016884932.1
XM_017029444.1 Intron XP_016884933.1
XM_017029445.1 Intron XP_016884934.1
XM_017029446.1 Intron XP_016884935.1
XM_017029447.1 Intron XP_016884936.1
XM_017029448.1 Intron XP_016884937.1
XM_017029449.1 Intron XP_016884938.1

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