Product Details

SNP ID
rs146989129
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:46671542 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCCTCCTGTGTGGTTGGGGTCCAT[C/T]ATGTCACGGATCAGGTGGATCTCGG
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 2823 Missense Mutation NP_001177636.1
NM_147129.4 2823 Missense Mutation NP_667340.2
XM_005265025.1 2823 Missense Mutation XP_005265082.1
XM_006713091.2 2823 Intron XP_006713154.1
XM_006713093.3 2823 Intron XP_006713156.1
XM_006713094.3 2823 Intron XP_006713157.1
XM_011533572.2 2823 Intron XP_011531874.1
XM_017006120.1 2823 Intron XP_016861609.1

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