Product Details

SNP ID

rs148519712

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:205791622 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCCCAGTGCCAAGCAGGTCCCCCA[C/G]AGCAGTCAAGTATGGGATGGAGAAG

Phenotype

MIM: 610801

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SLC41A1 PubMed Links

Gene Details

Gene

SLC41A1

Gene Name

solute carrier family 41 member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173854.5	2488	Missense Mutation	CTG,GTG	L485V	NP_776253.3
XM_005245069.2	2488	Missense Mutation	CTG,GTG	L485V	XP_005245126.1

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