ClinVar

NM_024411.5(PDYN):c.106G>T (p.Gly36Cys)

Genes:

PDYN-AS1:PDYN antisense RNA 1 [Gene - HGNC]
PDYN:prodynorphin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

20p13

Genomic location:

• Chr20: 1982979 (on Assembly GRCh38)
• Chr20: 1963625 (on Assembly GRCh37)

Preferred name:

NM_024411.5(PDYN):c.106G>T (p.Gly36Cys)

HGVS:

• NC_000020.11:g.1982979C>A
• NG_028027.1:g.16267G>T
• NM_001190892.1:c.106G>T
• NM_001190898.3:c.106G>T
• NM_001190899.2:c.106G>T
• NM_001190900.1:c.106G>T
• NM_024411.5:c.106G>TMANE SELECT
• NP_001177821.1:p.Gly36Cys
• NP_001177827.1:p.Gly36Cys
• NP_001177828.1:p.Gly36Cys
• NP_001177829.1:p.Gly36Cys
• NP_077722.1:p.Gly36Cys
• LRG_667t1:c.106G>T
• LRG_667:g.16267G>T
• LRG_667p1:p.Gly36Cys
• NC_000020.10:g.1963625C>A
• NM_024411.4:c.106G>T

This HGVS expression did not pass validation

Protein change:

G36C

Links:

dbSNP: rs149056587

NCBI 1000 Genomes Browser:

rs149056587

Molecular consequence:

• NM_001190892.1:c.106G>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001190898.3:c.106G>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001190899.2:c.106G>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001190900.1:c.106G>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_024411.5:c.106G>T - missense variant - [Sequence Ontology: SO:0001583]