Product Details

SNP ID
rs9989626
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.18:606495 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCATGACATTTCTTTGCAAAGTCCC[A/G]GAACCCACAGCTCTGAGACTCTGGC
Phenotype
MIM: 616990
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
CLUL1 PubMed Links

Gene Details

Gene
CLUL1
Gene Name
clusterin like 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001289036.1 Intron NP_001275965.1
NM_001318522.1 Intron NP_001305451.1
NM_014410.4 Intron NP_055225.1
NM_199167.1 Intron NP_954636.1
XM_005258103.3 Intron XP_005258160.1
XM_006722322.2 Intron XP_006722385.1
XM_011525648.2 Intron XP_011523950.1
XM_011525649.1 Intron XP_011523951.1
XM_011525651.2 Intron XP_011523953.1
XM_011525652.1 Intron XP_011523954.1
XM_011525653.2 Intron XP_011523955.1
XM_017025707.1 Intron XP_016881196.1

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