Product Details

SNP ID

rs112511627

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:18081280 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGGACGTCTCTTTTCTTTGAGTT[C/T]GAAGTTTATCAGGATGTCCTTGATA

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	736	Missense Mutation	AAA,GAA	K176E	NP_001273130.1
NM_024730.3	736	Missense Mutation	AAA,GAA	K177E	NP_079006.1

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