Product Details

SNP ID
rs147145432
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:121664611 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTCGCTTCCATCCAACGCCACTCC[A/G]GGTCTGAAAGAAAAATGTGAAAGTC
Phenotype
MIM: 602500 MIM: 601306
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
GOLGB1 PubMed Links

Gene Details

Gene
GOLGB1
Gene Name
golgin B1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001256486.1 10154 Missense Mutation NP_001243415.1
NM_001256487.1 10154 Missense Mutation NP_001243416.1
NM_001256488.1 10154 Missense Mutation NP_001243417.1
NM_004487.4 10154 Missense Mutation NP_004478.3
XM_005247371.4 10154 Missense Mutation XP_005247428.1
XM_005247372.4 10154 Missense Mutation XP_005247429.1
XM_005247373.1 10154 Missense Mutation XP_005247430.1
XM_006713587.1 10154 Missense Mutation XP_006713650.1
XM_006713588.1 10154 Missense Mutation XP_006713651.1
XM_006713589.1 10154 Missense Mutation XP_006713652.1
XM_006713590.1 10154 Missense Mutation XP_006713653.1
XM_006713591.1 10154 Missense Mutation XP_006713654.1
XM_011512699.2 10154 Missense Mutation XP_011511001.1
XM_017006189.1 10154 Missense Mutation XP_016861678.1
XM_017006190.1 10154 Missense Mutation XP_016861679.1
XM_017006191.1 10154 Missense Mutation XP_016861680.1
XM_017006192.1 10154 Missense Mutation XP_016861681.1
XM_017006193.1 10154 Missense Mutation XP_016861682.1
XM_017006194.1 10154 Missense Mutation XP_016861683.1
XM_017006195.1 10154 Missense Mutation XP_016861684.1
Gene
HCLS1
Gene Name
hematopoietic cell-specific Lyn substrate 1
There are no transcripts associated with this gene.

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