Product Details

SNP ID
rs7591759
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:178828240 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCCCTAAAAACGTTTCCAGAATCCA[C/T]AGGAAATTCACACAGACAGAGAAGC
Phenotype
MIM: 616031
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CCDC141 PubMed Links

Gene Details

Gene
CCDC141
Gene Name
coiled-coil domain containing 141
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001316745.1 6286 Intron NP_001303674.1
NM_173648.3 6286 Intron NP_775919.3
XM_011510991.2 6286 Intron XP_011509293.1
XM_011510992.2 6286 UTR 3 XP_011509294.1
XM_011510993.2 6286 UTR 3 XP_011509295.1
XM_017003867.1 6286 UTR 3 XP_016859356.1
XM_017003868.1 6286 UTR 3 XP_016859357.1
XM_017003869.1 6286 UTR 3 XP_016859358.1
XM_017003870.1 6286 UTR 3 XP_016859359.1
XM_017003871.1 6286 Intron XP_016859360.1

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