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SNP ID

rs200101942

Assay Type

Functionally tested

NCBI dbSNP Submissions

3

Location

Chr.1:6192959 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGAGAAAGGCACCTCGGATGTCAC[A/G]GTGATCTTGCTCTTGCTCCTTTCGA

Phenotype

MIM: 180474

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RPL22 PubMed Links

Gene Details

Gene

RPL22

Gene Name

ribosomal protein L22

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000983.3	259	Silent Mutation			NP_000974.1

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