Variant #0000558288 (NC_000016.9:g.4848622A>G, NM_024589.1:c.479T>C (ROGDI))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.4848622A>G
DNA change (hg38) g.4798621A>G
Published as ROGDI(NM_024589.3):c.479T>C (p.L160P)
ISCN -
DB-ID GLYR1_000003
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMIM22 NM_001253790.1 ?/. - c.*2390A>G r.(=) p.(=)
ROGDI NM_024589.1 ?/. - c.479T>C r.(?) p.(Leu160Pro)
GLYR1 NM_032569.3 ?/. - c.*6615T>C r.(=) p.(=)
SEPT12 NM_144605.4 ?/. - c.-10364T>C r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.