Product Details

SNP ID

hCV28012639

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:46671175 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACCCACCTCCCAACCCAGAGGAGG[C/G]GTGTCTCCAACTCAGCCCTCAGCCA

Phenotype

MIM: 612402

Polymorphism

C/G, Transversion 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		Intron			NP_001177636.1
NM_147129.4		Intron			NP_667340.2

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