Product Details

SNP ID
rs143694876
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:72184095 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCACTTCTCAAGCAGGGTCAGAGC[A/G]GTCACTGGGTTTACCCGGAGGTACT
Phenotype
MIM: 607880
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
EXOC6B PubMed Links

Gene Details

Gene
EXOC6B
Gene Name
exocyst complex component 6B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001321729.1 1713 Silent Mutation ACC,ACT T763T NP_001308658.1
NM_001321730.1 1713 Silent Mutation ACC,ACT T718T NP_001308659.1
NM_001321731.1 1713 Silent Mutation ACC,ACT T763T NP_001308660.1
NM_001321733.1 1713 Silent Mutation ACC,ACT T718T NP_001308662.1
NM_001321734.1 1713 Silent Mutation ACC,ACT T650T NP_001308663.1
NM_015189.2 1713 Silent Mutation ACC,ACT T763T NP_056004.1
XM_005264224.1 1713 Silent Mutation ACC,ACT T431T XP_005264281.1
XM_011532711.2 1713 Intron XP_011531013.1
XM_011532712.2 1713 Intron XP_011531014.1
XM_017003641.1 1713 Silent Mutation ACC,ACT T581T XP_016859130.1
XM_017003642.1 1713 Silent Mutation ACC,ACT T431T XP_016859131.1

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