Product Details

SNP ID

rs13462

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:170866460 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCGTAGGTCTCCTTGTCAGATGCAA[C/A]CACTCGAAGCCAATCACGAAGATTG

Phenotype

Polymorphism

C/A, Transversion substitution

Allele Nomenclature

Literature Links

RPL22L1 PubMed Links

Gene Details

Gene

RPL22L1

Gene Name

ribosomal protein L22 like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001099645.1	375	Missense Mutation	GTT,TTT	V97F	NP_001093115.1
NM_001320451.1	375	Missense Mutation	GTT,TTT	V96F	NP_001307380.1

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