Variant #0000518484 (NC_000003.11:g.170584183_170584184del, NM_001099645.1:c.356_357del (RPL22L1))

Chromosome 3
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.170584183_170584184del
DNA change (hg38) g.170866394_170866395del
Published as RPL22L1(NM_001099645.2):c.356_357delAG (p.E119Vfs*61)
ISCN -
DB-ID RPL22L1_000001
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-16 08:49:08 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL22L1 NM_001099645.1 ?/. - c.356_357del r.(?) p.(Glu119ValfsTer61)


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