Variant #0000523514 (NC_000004.11:g.89013403_89013425dup, NM_004827.2:c.1930_1952dup (ABCG2))

Chromosome 4
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.89013403_89013425dup
DNA change (hg38) g.88092251_88092273dup
Published as ABCG2(NM_004827.2):c.1930_1952dupGCCTACCTGAAATTGTTATTTCT (p.K652Pfs*3)
ISCN -
DB-ID ABCG2_000002
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 13:35:10 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCG2 NM_004827.2 -/. - c.1930_1952dup r.(?) p.(Lys652ProfsTer3)


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