Product Details

SNP ID
rs201068807
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:93131343 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAACAGATATTACTGGTATTTTTAT[C/T]TTTTCCTCTGTTCCATATTCTACAG
Phenotype
MIM: 611170
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SAMD9L PubMed Links

Gene Details

Gene
SAMD9L
Gene Name
sterile alpha motif domain containing 9 like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001303496.1 4667 Silent Mutation NP_001290425.1
NM_001303497.1 4667 Silent Mutation NP_001290426.1
NM_001303498.1 4667 Silent Mutation NP_001290427.1
NM_001303500.1 4667 Silent Mutation NP_001290429.1
NM_152703.3 4667 Silent Mutation NP_689916.2
XM_005250193.3 4667 Silent Mutation XP_005250250.1
XM_006715890.1 4667 Silent Mutation XP_006715953.1
XM_011515903.2 4667 Silent Mutation XP_011514205.1
XM_017011822.1 4667 Silent Mutation XP_016867311.1
XM_017011823.1 4667 Silent Mutation XP_016867312.1

View Full Product Details