Product Details

SNP ID
rs1802247
Assay Type
Functionally tested
NCBI dbSNP Submissions
1
Location
Chr.1:54036642 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAACATACTGCTCCACAGCTGTAG[C/T]AACAGTTGCACAACAAATCCAAAGC
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
TMEM59 PubMed Links

Gene Details

Gene
TMEM59
Gene Name
transmembrane protein 59
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001305043.1 707 Missense Mutation ACT,GCT T263A NP_001291972.1
NM_001305049.1 707 Missense Mutation ACT,GCT T132A NP_001291978.1
NM_001305050.1 707 Missense Mutation ACT,GCT T196A NP_001291979.1
NM_001305051.1 707 Missense Mutation ACT,GCT T131A NP_001291980.1
NM_001305052.1 707 Missense Mutation ACT,GCT T131A NP_001291981.1
NM_001305066.1 707 Intron NP_001291995.1
NM_004872.4 707 Missense Mutation ACT,GCT T262A NP_004863.2
XM_006711051.1 707 Missense Mutation ACT,GCT T195A XP_006711114.1

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