Variant #0000791286 (NC_000002.11:g.(?_43991388)_(44102695_?)del, NM_022436.2:c.-140_*644{0} (ABCG5))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_43991388)_(44102695_?)del
DNA change (hg38) -
Published as g.43991388_44102695del
ISCN -
DB-ID ABCG5_000258
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Wenjuan Qiu
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Wenjuan Qiu
Date created 2021-07-21 04:33:22 +02:00 (CEST)
Date last edited 2022-07-22 10:58:53 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCG5 NM_022436.2 +?/. -1_13_ c.-140_*644{0} r.0? p.0?



Screenings

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