Product Details

SNP ID

rs200461678

Assay Type

Functionally Tested

NCBI dbSNP Submissions

1

Location

Chr.3:187698974 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGTGGAAGAGGATGACCACATGGG[C/G]AGACTGCCAGGTGTGCCAGCACCAG

Phenotype

MIM: 609138

Polymorphism

C/G, 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	776	Missense Mutation	CCC,GCC	P68A	NP_001004312.2
XM_017006301.1	776	Missense Mutation	CCC,GCC	P68A	XP_016861790.1
XM_017006302.1	776	Missense Mutation	CCC,GCC	P68A	XP_016861791.1

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