Variant #0000863026 (NC_000012.11:g.50498520T>C, NM_005276.3:c.205T>C (GPD1))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.50498520T>C
DNA change (hg38) -
Published as GPD1(NM_005276.3):c.205T>C (p.L69=)
ISCN -
DB-ID COX14_000087
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) 0.00015 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCD1 NM_003076.4 -?/. - c.*5737T>C r.(=) p.(=)
GPD1 NM_005276.3 -?/. - c.205T>C r.(?) p.(Leu69=)
COX14 NM_032901.3 -?/. - c.-7573T>C r.(?) p.(=)


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