Variant #0000883619 (NC_000001.10:g.8421118_8421129del, NM_001042681.1:c.2439_2450del (RERE))

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.8421118_8421129del
DNA change (hg38) -
Published as RERE(NM_012102.4):c.2439_2450delACCGCATCCCCC (p.P817_P820del)
ISCN -
DB-ID RERE_000073
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RERE NM_001042681.1 ?/. - c.2439_2450del r.(?) p.(Pro817_Pro820del)


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