Variant #0000504927 (NC_000001.10:g.204125485_204125492dup, NC_000001.10(NM_000537.3):c.819-25_819-18dup (REN))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.204125485_204125492dup
DNA change (hg38) g.204156357_204156364dup
Published as REN(NM_000537.4):c.819-25_819-18dupTCTGTCTG
ISCN -
DB-ID ETNK2_000004
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
REN NM_000537.3 -/. - c.819-25_819-18dup r.(=) p.(=)
ETNK2 NM_018208.2 -/. - c.-4492_-4485dup r.(?) p.(=)


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