ClinVar

NM_014953.5(DIS3):c.1211G>A (p.Gly404Asp)

Gene:

DIS3:DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

13q21.33

Genomic location:

• Chr13: 72773712 (on Assembly GRCh38)
• Chr13: 73347850 (on Assembly GRCh37)

Preferred name:

NM_014953.5(DIS3):c.1211G>A (p.Gly404Asp)

HGVS:

• NC_000013.11:g.72773712C>T
• NM_001128226.3:c.1121G>A
• NM_001322348.2:c.842G>A
• NM_001322349.2:c.725G>A
• NM_014953.5:c.1211G>AMANE SELECT
• NP_001121698.1:p.Gly374Asp
• NP_001309277.1:p.Gly281Asp
• NP_001309278.1:p.Gly242Asp
• NP_055768.3:p.Gly404Asp
• NC_000013.10:g.73347850C>T
• NM_014953.3:c.1211G>A

This HGVS expression did not pass validation

Protein change:

G242D

Molecular consequence:

• NM_001128226.3:c.1121G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001322348.2:c.842G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001322349.2:c.725G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_014953.5:c.1211G>A - missense variant - [Sequence Ontology: SO:0001583]