Product Details

SNP ID
rs3827495
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:46670017 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCTGCACAAATCCACCCTCTCCCTA[C/T]GCTTTGCCCTGGACACTTTCAGAAC
Phenotype
MIM: 612402
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ALS2CL PubMed Links

Gene Details

Gene
ALS2CL
Gene Name
ALS2 C-terminal like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001190707.1 3925 UTR 3 NP_001177636.1
NM_147129.4 3925 UTR 3 NP_667340.2
XM_005265025.1 3925 UTR 3 XP_005265082.1
XM_006713091.2 3925 Intron XP_006713154.1
XM_006713093.3 3925 Intron XP_006713156.1
XM_006713094.3 3925 Intron XP_006713157.1
XM_011533572.2 3925 Intron XP_011531874.1
XM_017006120.1 3925 Intron XP_016861609.1

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