Variant #0001033333 (NC_000002.11:g.44021664T>C, NM_022436.2:c.*18591A>G (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.44021664T>C
DNA change (hg38) -
Published as DYNC2LI1(NM_016008.4):c.389T>C (p.(Leu130Pro))
ISCN -
DB-ID ABCG5_000377
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) 0.0002 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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.389T>C r.(?) p.(Leu130Pro)
ABCG5 NM_022436.2 ?/. - c.*18591A>G r.(=) p.(=)


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