Product Details

SNP ID

rs150455107

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:1980451 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCCACTTGAGCTTGGGACGAATGC[A/G]CCGCAAGAAGCCCCCATAGCGTTTG

Phenotype

MIM: 131340

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

LOC727993 PubMed Links

Gene Details

Gene

LOC727993

Gene Name

uncharacterized LOC727993

There are no transcripts associated with this gene.

Gene

PDYN

Gene Name

prodynorphin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001190892.1	912	Missense Mutation	CGC,TGC	R213C	NP_001177821.1
NM_001190898.2	912	Missense Mutation	CGC,TGC	R213C	NP_001177827.1
NM_001190899.2	912	Missense Mutation	CGC,TGC	R213C	NP_001177828.1
NM_001190900.1	912	Missense Mutation	CGC,TGC	R213C	NP_001177829.1
NM_024411.4	912	Missense Mutation	CGC,TGC	R213C	NP_077722.1
XM_011529244.1	912	Missense Mutation	CGC,TGC	R213C	XP_011527546.1
XM_011529245.1	912	Missense Mutation	CGC,TGC	R213C	XP_011527547.1
XM_011529246.2	912	Missense Mutation	CGC,TGC	R213C	XP_011527548.1
XM_011529247.1	912	Missense Mutation	CGC,TGC	R213C	XP_011527549.1
XM_011529248.1	912	Missense Mutation	CGC,TGC	R213C	XP_011527550.1
XM_011529249.2	912	Missense Mutation	CGC,TGC	R213C	XP_011527551.1
XM_011529250.2	912	Missense Mutation	CGC,TGC	R213C	XP_011527552.1
XM_017027878.1	912	Missense Mutation	CGC,TGC	R213C	XP_016883367.1

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