Product Details

SNP ID

rs941048

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:18081322 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCTTGATAATTCTGATAAACATCA[C/T]TTCCACCTCCAGAGACTGCTCTGCT

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	694	Missense Mutation	ATG,GTG	M162V	NP_001273130.1
NM_024730.3	694	Missense Mutation	ATG,GTG	M163V	NP_079006.1

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