Variant #0001034608 (NC_000004.11:g.5710195dup, NM_153717.2:c.-2913dup (EVC))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.5710195dup
DNA change (hg38) -
Published as EVC2(NM_147127.5):c.50dup (p.(Leu18Serfs*38))
ISCN -
DB-ID EVC_000187
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EVC2 NM_147127.4 +?/. - c.50dup r.(?) p.(Leu18Serfs*38)
EVC NM_153717.2 +?/. - c.-2913dup r.(?) p.(=)


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