Product Details

SNP ID
rs201207995
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:72184104 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAAGCAGGGTCAGAGCAGTCACTGG[A/G]TTTACCCGGAGGTACTTGCAGTTGG
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 1704 Silent Mutation AAC,AAT N760N NP_001308658.1
NM_001321730.1 1704 Silent Mutation AAC,AAT N715N NP_001308659.1
NM_001321731.1 1704 Silent Mutation AAC,AAT N760N NP_001308660.1
NM_001321733.1 1704 Silent Mutation AAC,AAT N715N NP_001308662.1
NM_001321734.1 1704 Silent Mutation AAC,AAT N647N NP_001308663.1
NM_015189.2 1704 Silent Mutation AAC,AAT N760N NP_056004.1
XM_005264224.1 1704 Silent Mutation AAC,AAT N428N XP_005264281.1
XM_011532711.2 1704 Intron XP_011531013.1
XM_011532712.2 1704 Intron XP_011531014.1
XM_017003641.1 1704 Silent Mutation AAC,AAT N578N XP_016859130.1
XM_017003642.1 1704 Silent Mutation AAC,AAT N428N XP_016859131.1

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