Variant #0001050408 (NC_000001.10:g.204124147_204124153del, NM_000537.3:c.1212_1218del (REN))

Chromosome 1
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.204124147_204124153del
DNA change (hg38) -
Published as REN(NM_000537.4):c.1212_1218del (p.(Leu404Phefs*57))
ISCN -
DB-ID ETNK2_000009
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
REN NM_000537.3 ?/. - c.1212_1218del r.(?) p.(Leu404Phefs*57)
ETNK2 NM_018208.2 ?/. - c.-3173_-3167del r.(?) p.(=)


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