Product Details

SNP ID

rs151100410

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:18081261 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCCATTGATTTAGATCCACTGGGA[C/T]GTCTCTTTTCTTTGAGTTTGAAGTT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RERGL PubMed Links

Gene Details

Gene

RERGL

Gene Name

RERG like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286201.1	755	Missense Mutation	CAT,CGT	H182R	NP_001273130.1
NM_024730.3	755	Missense Mutation	CAT,CGT	H183R	NP_079006.1

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