Variant #0000992856 (NC_000002.11:g.44041651A>G, NM_022436.2:c.1727T>C (ABCG5))

Chromosome 2
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.44041651A>G
DNA change (hg38) -
Published as ABCG5(NM_022436.3):c.1727T>C (p.V576A), DYNC2LI1(NM_001348913.2):c.*15+3988A>G
ISCN -
DB-ID ABCG5_000351
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) 8.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DYNC2LI1 NM_016008.3 ?/. - c.*4745A>G r.(=) p.(=)
ABCG5 NM_022436.2 ?/. - c.1727T>C r.(?) p.(Val576Ala)


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