Variant #0000545992 (NC_000011.9:g.831534G>C, NC_000011.9(NM_173584.3):c.859-1G>C (EFCAB4A))

Chromosome 11
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.831534G>C
DNA change (hg38) g.831534G>C
Published as EFCAB4A(NM_173584.4):c.859-1G>C (p.?)
ISCN -
DB-ID CD151_000011
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 View details
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 2020-06-29 13:03:07 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPLP2 NM_001004.3 ?/. - c.*18698G>C r.(=) p.(=)
CD151 NM_004357.4 ?/. - c.-1562G>C r.(?) p.(=)
PNPLA2 NM_020376.3 ?/. - c.*6672G>C r.(=) p.(=)
EFCAB4A NM_173584.3 ?/. - c.859-1G>C r.spl? p.?


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