ClinVar

NM_006266.4(RALGDS):c.2595C>T (p.Asn865=)

Gene:

RALGDS:ral guanine nucleotide dissociation stimulator [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9q34.13

Genomic location:

• Chr9: 133098737 (on Assembly GRCh38)
• Chr9: 135974124 (on Assembly GRCh37)

Preferred name:

NM_006266.4(RALGDS):c.2595C>T (p.Asn865=)

HGVS:

• NC_000009.12:g.133098737G>A
• NM_001042368.3:c.2430C>T
• NM_001271774.2:c.2508C>T
• NM_001271775.2:c.2592C>T
• NM_001271776.2:c.2559C>T
• NM_006266.4:c.2595C>TMANE SELECT
• NP_001035827.1:p.Asn810=
• NP_001258703.1:p.Asn836=
• NP_001258704.1:p.Asn864=
• NP_001258705.1:p.Asn853=
• NP_006257.1:p.Asn865=
• NC_000009.11:g.135974124G>A
• NM_006266.3:c.2595C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs745773402

NCBI 1000 Genomes Browser:

rs745773402

Molecular consequence:

• NM_001042368.3:c.2430C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001271774.2:c.2508C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001271775.2:c.2592C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001271776.2:c.2559C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_006266.4:c.2595C>T - synonymous variant - [Sequence Ontology: SO:0001819]