Product Details

SNP ID
rs144122877
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:81802476 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCTGTTTCTGACACATCCAGTGAT[C/T]CTTCAGGTTCTAAAGACAATGTTCT
Phenotype
MIM: 614903
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SNX16 PubMed Links

Gene Details

Gene
SNX16
Gene Name
sorting nexin 16
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_022133.3 1103 Missense Mutation GAA,GGA E281G NP_071416.2
NM_152836.2 1103 Missense Mutation GAA,GGA E281G NP_690049.1
NM_152837.2 1103 Missense Mutation GAA,GGA E252G NP_690050.1
XM_005251282.4 1103 Missense Mutation GAA,GGA E252G XP_005251339.1
XM_005251283.2 1103 Missense Mutation GAA,GGA E252G XP_005251340.1
XM_011517574.2 1103 Missense Mutation GAA,GGA E124G XP_011515876.1

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