Product Details

SNP ID

rs1880095

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:187699866 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTAGAGTCCCAGTCTCAGGAAGTGT[G/T]GTGGGTGGTAGCCTGGGGCTCATCT

Phenotype

MIM: 609138

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

LOC100131635 PubMed Links

Gene Details

Gene

LOC100131635

Gene Name

hCG1645011-like

There are no transcripts associated with this gene.

Gene

RTP2

Gene Name

receptor transporter protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004312.2		Intron			NP_001004312.2
XM_017006301.1		Intron			XP_016861790.1
XM_017006302.1		Intron			XP_016861791.1

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