Variant #0000545991 (NC_000011.9:g.830709G>C, NM_173584.3:c.782G>C (EFCAB4A))

Chromosome 11
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.830709G>C
DNA change (hg38) g.830709G>C
Published as EFCAB4A(NM_173584.4):c.782G>C (p.(Arg261Pro))
ISCN -
DB-ID CD151_000010
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPLP2 NM_001004.3 -?/. - c.*17873G>C r.(=) p.(=)
CD151 NM_004357.4 -?/. - c.-2387G>C r.(?) p.(=)
PNPLA2 NM_020376.3 -?/. - c.*5847G>C r.(=) p.(=)
EFCAB4A NM_173584.3 -?/. - c.782G>C r.(?) p.(Arg261Pro)


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