Product Details

SNP ID

rs121909065

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:71719903 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGATCGAAGCGCTGCAAGAAGTCTT[C/G]AAGAAGCTCAAGAGTAAACGTGTTC

Phenotype

MIM: 602606

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

CARTPT PubMed Links

Gene Details

Gene

CARTPT

Gene Name

CART prepropeptide

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004291.3	314	Missense Mutation	TTC,TTG	F61L	NP_004282.1

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