Variant #0000975553 (NC_000003.11:g.127786290T>G, NM_021937.3:c.-86061T>G (EEFSEC))

Chromosome 3
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.127786290T>G
DNA change (hg38) -
Published as SEC61A1(NM_013336.4):c.1002T>G (p.R334=)
ISCN -
DB-ID RUVBL1_000014
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) 0.00039 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RUVBL1 NM_003707.2 -?/. - c.*13803A>C r.(=) p.(=)
SEC61A1 NM_013336.3 -?/. - c.1002T>G r.(?) p.(=)
EEFSEC NM_021937.3 -?/. - c.-86061T>G r.(?) p.(=)


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