Product Details

SNP ID

rs200801104

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:18081436 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCTCTCGCACATGACAAAGATCTC[A/G]TTTGTTGCCAACCAAAAACACTGCT

Phenotype

Polymorphism

A/G, 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	580	Nonsense Mutation	CGA,TGA	R124*	NP_001273130.1
NM_024730.3	580	Nonsense Mutation	CGA,TGA	R125*	NP_079006.1

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