Variant #0000719323 (NC_000003.11:g.196229726_196229739del, NC_000003.11(NM_152617.3):c.301+7_301+20del (RNF168))

Chromosome 3
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.196229726_196229739del
DNA change (hg38) -
Published as RNF168(NM_152617.3):c.301+7_301+20delAAACCATGGCGTGT
ISCN -
DB-ID C3orf43_000006
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C3orf43 NM_001077657.1 -?/. - c.*5021_*5034del r.(=) p.(=)
RNF168 NM_152617.3 -?/. - c.301+7_301+20del r.(=) p.(=)


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