Variant #0000515831 (NC_000002.11:g.44041659C>A, NM_022436.2:c.1719G>T (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.44041659C>A
DNA change (hg38) g.43814520C>A
Published as ABCG5(NM_022436.3):c.1719G>T (p.E573D), DYNC2LI1(NM_001348913.2):c.*15+3996C>A
ISCN -
DB-ID ABCG5_000057
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 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DYNC2LI1 NM_016008.3 ?/. - c.*4753C>A r.(=) p.(=)
ABCG5 NM_022436.2 ?/. - c.1719G>T r.(?) p.(Glu573Asp)


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