Variant #0000613769 (NC_000011.9:g.829478_829480dup, NM_173584.3:c.396_398dup (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.829478_829480dup
DNA change (hg38) g.829478_829480dup
Published as EFCAB4A(NM_173584.4):c.387_388insGAG (p.(Asp129_Glu130insGlu))
ISCN -
DB-ID CD151_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) 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPLP2 NM_001004.3 -?/. - c.*16642_*16644dup r.(=) p.(=)
CD151 NM_004357.4 -?/. - c.-3618_-3616dup r.(?) p.(=)
PNPLA2 NM_020376.3 -?/. - c.*4616_*4618dup r.(=) p.(=)
EFCAB4A NM_173584.3 -?/. - c.396_398dup r.(?) p.(Glu136dup)


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