Product Details

SNP ID
rs201290666
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:36579906 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTACGACGAGATAGCCCAGTGCCTA[A/G]TGTCTGTGCCGCCTACCAGGCAGAG
Phenotype
MIM: 615626
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C15orf41 PubMed Links

Gene Details

Gene
C15orf41
Gene Name
chromosome 15 open reading frame 41
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001130010.2 304 Missense Mutation ATG,GTG M16V NP_001123482.1
NM_001290232.1 304 Intron NP_001277161.1
NM_001290233.1 304 Missense Mutation ATG,GTG M16V NP_001277162.1
NM_001321756.1 304 UTR 5 NP_001308685.1
NM_001321757.1 304 UTR 5 NP_001308686.1
NM_001321758.1 304 Missense Mutation ATG,GTG M16V NP_001308687.1
NM_001321759.1 304 Missense Mutation ATG,GTG M16V NP_001308688.1
NM_001321760.1 304 Missense Mutation ATG,GTG M16V NP_001308689.1
NM_001321761.1 304 Missense Mutation ATG,GTG M16V NP_001308690.1
NM_032499.5 304 Intron NP_115888.1
XM_011522111.1 304 Missense Mutation ATG,GTG M16V XP_011520413.1
XM_017022676.1 304 Missense Mutation ATG,GTG M16V XP_016878165.1
XM_017022677.1 304 Missense Mutation ATG,GTG M16V XP_016878166.1

View Full Product Details