Variant #0000620702 (NC_000001.10:g.8421116_8421127dup, NM_001042681.1:c.2449_2460dup (RERE))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.8421116_8421127dup
DNA change (hg38) g.8361056_8361067dup
Published as RERE(NM_012102.4):c.2449_2460dupCCGCCGCATCCC (p.P817_P820dup)
ISCN -
DB-ID RERE_000036
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 2019-12-06 12:43:26 +01:00 (CET)
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     
RERE NM_001042681.1 -?/. - c.2449_2460dup r.(?) p.(Pro817_Pro820dup)


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