Product Details

SNP ID

rs200037738

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:1980441 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTCTGGTTGTCCCACTTGAGCTTG[A/G]GACGAATGCGCCGCAAGAAGCCCCC

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	922	Missense Mutation	CCC,CTC	P216L	NP_001177821.1
NM_001190898.2	922	Missense Mutation	CCC,CTC	P216L	NP_001177827.1
NM_001190899.2	922	Missense Mutation	CCC,CTC	P216L	NP_001177828.1
NM_001190900.1	922	Missense Mutation	CCC,CTC	P216L	NP_001177829.1
NM_024411.4	922	Missense Mutation	CCC,CTC	P216L	NP_077722.1
XM_011529244.1	922	Missense Mutation	CCC,CTC	P216L	XP_011527546.1
XM_011529245.1	922	Missense Mutation	CCC,CTC	P216L	XP_011527547.1
XM_011529246.2	922	Missense Mutation	CCC,CTC	P216L	XP_011527548.1
XM_011529247.1	922	Missense Mutation	CCC,CTC	P216L	XP_011527549.1
XM_011529248.1	922	Missense Mutation	CCC,CTC	P216L	XP_011527550.1
XM_011529249.2	922	Missense Mutation	CCC,CTC	P216L	XP_011527551.1
XM_011529250.2	922	Missense Mutation	CCC,CTC	P216L	XP_011527552.1
XM_017027878.1	922	Missense Mutation	CCC,CTC	P216L	XP_016883367.1

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