Variant #0000719932 (NC_000004.11:g.5710046_5710050dup, NM_153717.2:c.-3062_-3058dup (EVC))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.5710046_5710050dup
DNA change (hg38) -
Published as EVC2(NM_147127.4):c.194_198dupGGCGG (p.S67Gfs*17)
ISCN -
DB-ID EVC2_000133 See all 3 reported entries
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EVC2 NM_147127.4 +/. - c.194_198dup r.(?) p.(Ser67GlyfsTer17)
EVC NM_153717.2 +/. - c.-3062_-3058dup r.(?) p.(=)


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