Product Details

SNP ID

rs145717807

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:187698724 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGCAGGCCTCACAGAACTCTGCA[C/T]GATGCGGCCCGCTGTCCGGGCGGCT

Phenotype

MIM: 609138

Polymorphism

C/T, Transition 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	1026	Missense Mutation	CAT,CGT	H151R	NP_001004312.2
XM_017006301.1	1026	Missense Mutation	CAT,CGT	H151R	XP_016861790.1
XM_017006302.1	1026	Missense Mutation	CAT,CGT	H151R	XP_016861791.1

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