Variant #0000862732 (NC_000011.9:g.836380A>G, NM_173584.3:c.*4819A>G (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.836380A>G
DNA change (hg38) -
Published as CD151(NM_004357.4):c.214A>G (p.M72V)
ISCN -
DB-ID CD151_000016
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_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     
CD151 NM_004357.4 ?/. - c.214A>G r.(?) p.(Met72Val)
POLR2L NM_021128.4 ?/. - c.*3992T>C r.(=) p.(=)
EFCAB4A NM_173584.3 ?/. - c.*4819A>G r.(=) p.(=)


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